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queries/queries_genetics.jsonl

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+{"id": "genetics_T1_328", "domain": "genetics", "type": "T1_entity", "query": "What is Variant Classification?", "ground_truth": ["Variant Classification", "BIOINFO"], "concept_id": 328, "hop_depth": 0}
+{"id": "genetics_T1_58", "domain": "genetics", "type": "T1_entity", "query": "What is Telomere Structure?", "ground_truth": ["Telomere Structure", "GSTR"], "concept_id": 58, "hop_depth": 0}
+{"id": "genetics_T1_13", "domain": "genetics", "type": "T1_entity", "query": "What is X-Linked Dominant Pedigree?", "ground_truth": ["X-Linked Dominant Pedigree", "PED"], "concept_id": 13, "hop_depth": 0}
+{"id": "genetics_T1_380", "domain": "genetics", "type": "T1_entity", "query": "What is BRCA Genes?", "ground_truth": ["BRCA Genes", "CLIN"], "concept_id": 380, "hop_depth": 0}
+{"id": "genetics_T1_141", "domain": "genetics", "type": "T1_entity", "query": "What is Parametric Linkage?", "ground_truth": ["Parametric Linkage", "MAP"], "concept_id": 141, "hop_depth": 0}
+{"id": "genetics_T1_126", "domain": "genetics", "type": "T1_entity", "query": "What is Restriction Fragment Length?", "ground_truth": ["Restriction Fragment Length", "MAP"], "concept_id": 126, "hop_depth": 0}
+{"id": "genetics_T1_115", "domain": "genetics", "type": "T1_entity", "query": "What is Recombination Frequency?", "ground_truth": ["Recombination Frequency", "MAP"], "concept_id": 115, "hop_depth": 0}
+{"id": "genetics_T1_72", "domain": "genetics", "type": "T1_entity", "query": "What is Barr Body?", "ground_truth": ["Barr Body", "GSTR"], "concept_id": 72, "hop_depth": 0}
+{"id": "genetics_T1_378", "domain": "genetics", "type": "T1_entity", "query": "What is Microsatellite Instability?", "ground_truth": ["Microsatellite Instability", "CLIN"], "concept_id": 378, "hop_depth": 0}
+{"id": "genetics_T1_53", "domain": "genetics", "type": "T1_entity", "query": "What is Euchromatin?", "ground_truth": ["Euchromatin", "GSTR"], "concept_id": 53, "hop_depth": 0}
+{"id": "genetics_T1_347", "domain": "genetics", "type": "T1_entity", "query": "What is Mendelian Disease?", "ground_truth": ["Mendelian Disease", "CLIN"], "concept_id": 347, "hop_depth": 0}
+{"id": "genetics_T1_280", "domain": "genetics", "type": "T1_entity", "query": "What is Yeast Genetics?", "ground_truth": ["Yeast Genetics", "EXP"], "concept_id": 280, "hop_depth": 0}
+{"id": "genetics_T1_45", "domain": "genetics", "type": "T1_entity", "query": "What is Genomic Imprinting?", "ground_truth": ["Genomic Imprinting", "PED"], "concept_id": 45, "hop_depth": 0}
+{"id": "genetics_T1_303", "domain": "genetics", "type": "T1_entity", "query": "What is Phenotype Scoring?", "ground_truth": ["Phenotype Scoring", "EXP"], "concept_id": 303, "hop_depth": 0}
+{"id": "genetics_T1_217", "domain": "genetics", "type": "T1_entity", "query": "What is Specific Transcription Factor?", "ground_truth": ["Specific Transcription Factor", "REG"], "concept_id": 217, "hop_depth": 0}
+{"id": "genetics_T1_17", "domain": "genetics", "type": "T1_entity", "query": "What is Expressivity?", "ground_truth": ["Expressivity", "PED"], "concept_id": 17, "hop_depth": 0}
+{"id": "genetics_T1_16", "domain": "genetics", "type": "T1_entity", "query": "What is Incomplete Penetrance?", "ground_truth": ["Incomplete Penetrance", "PED"], "concept_id": 16, "hop_depth": 0}
+{"id": "genetics_T1_48", "domain": "genetics", "type": "T1_entity", "query": "What is Mosaicism?", "ground_truth": ["Mosaicism", "PED"], "concept_id": 48, "hop_depth": 0}
+{"id": "genetics_T1_112", "domain": "genetics", "type": "T1_entity", "query": "What is Genetic Linkage?", "ground_truth": ["Genetic Linkage", "MAP"], "concept_id": 112, "hop_depth": 0}
+{"id": "genetics_T1_120", "domain": "genetics", "type": "T1_entity", "query": "What is Three-Point Cross?", "ground_truth": ["Three-Point Cross", "MAP"], "concept_id": 120, "hop_depth": 0}
+{"id": "genetics_T1_259", "domain": "genetics", "type": "T1_entity", "query": "What is Cell Identity?", "ground_truth": ["Cell Identity", "REG"], "concept_id": 259, "hop_depth": 0}
+{"id": "genetics_T1_309", "domain": "genetics", "type": "T1_entity", "query": "What is Next-Gen Sequencing?", "ground_truth": ["Next-Gen Sequencing", "BIOINFO"], "concept_id": 309, "hop_depth": 0}
+{"id": "genetics_T1_14", "domain": "genetics", "type": "T1_entity", "query": "What is Carrier Probability?", "ground_truth": ["Carrier Probability", "PED"], "concept_id": 14, "hop_depth": 0}
+{"id": "genetics_T1_288", "domain": "genetics", "type": "T1_entity", "query": "What is RNA Interference Screen?", "ground_truth": ["RNA Interference Screen", "MAP"], "concept_id": 288, "hop_depth": 0}
+{"id": "genetics_T1_102", "domain": "genetics", "type": "T1_entity", "query": "What is Gene Family?", "ground_truth": ["Gene Family", "GVAR"], "concept_id": 102, "hop_depth": 0}
+{"id": "genetics_T1_367", "domain": "genetics", "type": "T1_entity", "query": "What is Precision Medicine?", "ground_truth": ["Precision Medicine", "CLIN"], "concept_id": 367, "hop_depth": 0}
+{"id": "genetics_T1_333", "domain": "genetics", "type": "T1_entity", "query": "What is NCBI Database?", "ground_truth": ["NCBI Database", "BIOINFO"], "concept_id": 333, "hop_depth": 0}
+{"id": "genetics_T1_360", "domain": "genetics", "type": "T1_entity", "query": "What is Presymptomatic Testing?", "ground_truth": ["Presymptomatic Testing", "CLIN"], "concept_id": 360, "hop_depth": 0}
+{"id": "genetics_T1_215", "domain": "genetics", "type": "T1_entity", "query": "What is Transcription Factor?", "ground_truth": ["Transcription Factor", "REG"], "concept_id": 215, "hop_depth": 0}
+{"id": "genetics_T1_113", "domain": "genetics", "type": "T1_entity", "query": "What is Recombination?", "ground_truth": ["Recombination", "MAP"], "concept_id": 113, "hop_depth": 0}
+{"id": "genetics_T1_230", "domain": "genetics", "type": "T1_entity", "query": "What is Feed-Forward Loop?", "ground_truth": ["Feed-Forward Loop", "REG"], "concept_id": 230, "hop_depth": 0}
+{"id": "genetics_T1_302", "domain": "genetics", "type": "T1_entity", "query": "What is Functional Genomics?", "ground_truth": ["Functional Genomics", "FOUND"], "concept_id": 302, "hop_depth": 0}
+{"id": "genetics_T1_143", "domain": "genetics", "type": "T1_entity", "query": "What is Recombination Hotspots?", "ground_truth": ["Recombination Hotspots", "MAP"], "concept_id": 143, "hop_depth": 0}
+{"id": "genetics_T1_415", "domain": "genetics", "type": "T1_entity", "query": "What is Science Communication?", "ground_truth": ["Science Communication", "ETHICS"], "concept_id": 415, "hop_depth": 0}
+{"id": "genetics_T1_446", "domain": "genetics", "type": "T1_entity", "query": "What is Computational Workflow?", "ground_truth": ["Computational Workflow", "BIOINFO"], "concept_id": 446, "hop_depth": 0}
+{"id": "genetics_T1_4", "domain": "genetics", "type": "T1_entity", "query": "What is Bayesian Reasoning?", "ground_truth": ["Bayesian Reasoning", "PROB"], "concept_id": 4, "hop_depth": 0}
+{"id": "genetics_T1_389", "domain": "genetics", "type": "T1_entity", "query": "What is Antisense Therapy?", "ground_truth": ["Antisense Therapy", "CLIN"], "concept_id": 389, "hop_depth": 0}
+{"id": "genetics_T1_413", "domain": "genetics", "type": "T1_entity", "query": "What is Genetic Literacy?", "ground_truth": ["Genetic Literacy", "ETHICS"], "concept_id": 413, "hop_depth": 0}
+{"id": "genetics_T1_82", "domain": "genetics", "type": "T1_entity", "query": "What is Tandem Repeat?", "ground_truth": ["Tandem Repeat", "GVAR"], "concept_id": 82, "hop_depth": 0}
+{"id": "genetics_T1_358", "domain": "genetics", "type": "T1_entity", "query": "What is Diagnostic Testing?", "ground_truth": ["Diagnostic Testing", "CLIN"], "concept_id": 358, "hop_depth": 0}
+{"id": "genetics_T1_175", "domain": "genetics", "type": "T1_entity", "query": "What is Quantitative Trait Locus?", "ground_truth": ["Quantitative Trait Locus", "QUANT"], "concept_id": 175, "hop_depth": 0}
+{"id": "genetics_T1_80", "domain": "genetics", "type": "T1_entity", "query": "What is Chromosomal Deletion?", "ground_truth": ["Chromosomal Deletion", "GVAR"], "concept_id": 80, "hop_depth": 0}
+{"id": "genetics_T1_111", "domain": "genetics", "type": "T1_entity", "query": "What is Linkage?", "ground_truth": ["Linkage", "FOUND"], "concept_id": 111, "hop_depth": 0}
+{"id": "genetics_T1_391", "domain": "genetics", "type": "T1_entity", "query": "What is Genetic Ethics?", "ground_truth": ["Genetic Ethics", "FOUND"], "concept_id": 391, "hop_depth": 0}
+{"id": "genetics_T1_173", "domain": "genetics", "type": "T1_entity", "query": "What is Concordance Rate?", "ground_truth": ["Concordance Rate", "QUANT"], "concept_id": 173, "hop_depth": 0}
+{"id": "genetics_T1_195", "domain": "genetics", "type": "T1_entity", "query": "What is Natural Selection?", "ground_truth": ["Natural Selection", "POP"], "concept_id": 195, "hop_depth": 0}
+{"id": "genetics_T1_50", "domain": "genetics", "type": "T1_entity", "query": "What is Germline Mosaicism?", "ground_truth": ["Germline Mosaicism", "PED"], "concept_id": 50, "hop_depth": 0}
+{"id": "genetics_T1_184", "domain": "genetics", "type": "T1_entity", "query": "What is False Discovery Rate?", "ground_truth": ["False Discovery Rate", "QUANT"], "concept_id": 184, "hop_depth": 0}
+{"id": "genetics_T1_434", "domain": "genetics", "type": "T1_entity", "query": "What is Metagenomics?", "ground_truth": ["Metagenomics", "FOUND"], "concept_id": 434, "hop_depth": 0}
+{"id": "genetics_T1_177", "domain": "genetics", "type": "T1_entity", "query": "What is Interval Mapping?", "ground_truth": ["Interval Mapping", "QUANT"], "concept_id": 177, "hop_depth": 0}
+{"id": "genetics_T2_319", "domain": "genetics", "type": "T2_dependency", "query": "What are the prerequisites for Genome Annotation?", "ground_truth": ["Genomics", "Sequence Alignment"], "concept_id": 319, "hop_depth": 1}
+{"id": "genetics_T2_139", "domain": "genetics", "type": "T2_dependency", "query": "What are the prerequisites for LOD Score?", "ground_truth": ["Linkage Analysis"], "concept_id": 139, "hop_depth": 1}
+{"id": "genetics_T2_425", "domain": "genetics", "type": "T2_dependency", "query": "What are the prerequisites for Machine Learning Variants?", "ground_truth": ["AI in Genomics", "Variant Calling"], "concept_id": 425, "hop_depth": 1}
+{"id": "genetics_T2_24", "domain": "genetics", "type": "T2_dependency", "query": "What are the prerequisites for Duplicate Epistasis?", "ground_truth": ["Epistasis"], "concept_id": 24, "hop_depth": 1}
+{"id": "genetics_T2_384", "domain": "genetics", "type": "T2_dependency", "query": "What are the prerequisites for Chromosomal Instability?", "ground_truth": ["Cancer Genetics", "Chromosomal Rearrangement"], "concept_id": 384, "hop_depth": 1}
+{"id": "genetics_T2_242", "domain": "genetics", "type": "T2_dependency", "query": "What are the prerequisites for RNA Interference?", "ground_truth": ["Post-Transcriptional Reg", "MicroRNA"], "concept_id": 242, "hop_depth": 1}
+{"id": "genetics_T2_283", "domain": "genetics", "type": "T2_dependency", "query": "What are the prerequisites for Zebrafish Genetics?", "ground_truth": ["Model Organism"], "concept_id": 283, "hop_depth": 1}
+{"id": "genetics_T2_66", "domain": "genetics", "type": "T2_dependency", "query": "What are the prerequisites for Epigenetics?", "ground_truth": ["Histone Modifications", "CpG Islands"], "concept_id": 66, "hop_depth": 1}
+{"id": "genetics_T2_199", "domain": "genetics", "type": "T2_dependency", "query": "What are the prerequisites for Stabilizing Selection?", "ground_truth": ["Natural Selection"], "concept_id": 199, "hop_depth": 1}
+{"id": "genetics_T2_42", "domain": "genetics", "type": "T2_dependency", "query": "What are the prerequisites for Genetic Background Effects?", "ground_truth": ["Epistasis", "Pleiotropy"], "concept_id": 42, "hop_depth": 1}
+{"id": "genetics_T2_291", "domain": "genetics", "type": "T2_dependency", "query": "What are the prerequisites for Gene Editing?", "ground_truth": ["CRISPR-Cas9"], "concept_id": 291, "hop_depth": 1}
+{"id": "genetics_T2_154", "domain": "genetics", "type": "T2_dependency", "query": "What are the prerequisites for Fine Structure Mapping?", "ground_truth": ["Genetic Map", "Intragenic Recombination"], "concept_id": 154, "hop_depth": 1}
+{"id": "genetics_T2_436", "domain": "genetics", "type": "T2_dependency", "query": "What are the prerequisites for Gene Regulation Atlas?", "ground_truth": ["Gene Regulatory Network", "Single-Cell Genomics"], "concept_id": 436, "hop_depth": 1}
+{"id": "genetics_T2_331", "domain": "genetics", "type": "T2_dependency", "query": "What are the prerequisites for Variant of Uncertain Sig?", "ground_truth": ["Variant Classification"], "concept_id": 331, "hop_depth": 1}
+{"id": "genetics_T2_326", "domain": "genetics", "type": "T2_dependency", "query": "What are the prerequisites for BED File Format?", "ground_truth": ["Genome Annotation"], "concept_id": 326, "hop_depth": 1}
+{"id": "genetics_T2_191", "domain": "genetics", "type": "T2_dependency", "query": "What are the prerequisites for Genotype Frequency?", "ground_truth": ["Allele Frequency"], "concept_id": 191, "hop_depth": 1}
+{"id": "genetics_T2_304", "domain": "genetics", "type": "T2_dependency", "query": "What are the prerequisites for Genetic Interaction?", "ground_truth": ["Epistasis", "Model Organism"], "concept_id": 304, "hop_depth": 1}
+{"id": "genetics_T2_101", "domain": "genetics", "type": "T2_dependency", "query": "What are the prerequisites for Ortholog?", "ground_truth": ["Gene Duplication", "Comparative Genomics"], "concept_id": 101, "hop_depth": 1}
+{"id": "genetics_T2_371", "domain": "genetics", "type": "T2_dependency", "query": "What are the prerequisites for Oncogene?", "ground_truth": ["Cancer Genetics"], "concept_id": 371, "hop_depth": 1}
+{"id": "genetics_T2_37", "domain": "genetics", "type": "T2_dependency", "query": "What are the prerequisites for Null Hypothesis in Genetics?", "ground_truth": ["Chi-Square Test"], "concept_id": 37, "hop_depth": 1}
+{"id": "genetics_T2_25", "domain": "genetics", "type": "T2_dependency", "query": "What are the prerequisites for Complementary Epistasis?", "ground_truth": ["Epistasis"], "concept_id": 25, "hop_depth": 1}
+{"id": "genetics_T2_349", "domain": "genetics", "type": "T2_dependency", "query": "What are the prerequisites for Genetic Counseling?", "ground_truth": ["Human Genetics", "Risk Assessment"], "concept_id": 349, "hop_depth": 1}
+{"id": "genetics_T2_120", "domain": "genetics", "type": "T2_dependency", "query": "What are the prerequisites for Three-Point Cross?", "ground_truth": ["Two-Point Cross"], "concept_id": 120, "hop_depth": 1}
+{"id": "genetics_T2_407", "domain": "genetics", "type": "T2_dependency", "query": "What are the prerequisites for Germline Editing Debate?", "ground_truth": ["Gene Editing Ethics"], "concept_id": 407, "hop_depth": 1}
+{"id": "genetics_T2_152", "domain": "genetics", "type": "T2_dependency", "query": "What are the prerequisites for Deletion Mapping?", "ground_truth": ["Chromosomal Deletion", "Genetic Map"], "concept_id": 152, "hop_depth": 1}
+{"id": "genetics_T2_449", "domain": "genetics", "type": "T2_dependency", "query": "What are the prerequisites for Systems Genetics?", "ground_truth": ["Gene Regulatory Network", "Quantitative Trait Locus", "Population Genetics"], "concept_id": 449, "hop_depth": 1}
+{"id": "genetics_T2_123", "domain": "genetics", "type": "T2_dependency", "query": "What are the prerequisites for Gene Order Determination?", "ground_truth": ["Three-Point Cross"], "concept_id": 123, "hop_depth": 1}
+{"id": "genetics_T2_54", "domain": "genetics", "type": "T2_dependency", "query": "What are the prerequisites for Heterochromatin?", "ground_truth": ["Chromosome Structure", "Chromatin"], "concept_id": 54, "hop_depth": 1}
+{"id": "genetics_T2_200", "domain": "genetics", "type": "T2_dependency", "query": "What are the prerequisites for Disruptive Selection?", "ground_truth": ["Natural Selection"], "concept_id": 200, "hop_depth": 1}
+{"id": "genetics_T2_146", "domain": "genetics", "type": "T2_dependency", "query": "What are the prerequisites for Gene Conversion?", "ground_truth": ["Recombination", "Mitotic Recombination"], "concept_id": 146, "hop_depth": 1}
+{"id": "genetics_T2_239", "domain": "genetics", "type": "T2_dependency", "query": "What are the prerequisites for Exon Skipping?", "ground_truth": ["Alternative Splicing"], "concept_id": 239, "hop_depth": 1}
+{"id": "genetics_T2_335", "domain": "genetics", "type": "T2_dependency", "query": "What are the prerequisites for UCSC Genome Browser?", "ground_truth": ["Genomic Databases"], "concept_id": 335, "hop_depth": 1}
+{"id": "genetics_T2_439", "domain": "genetics", "type": "T2_dependency", "query": "What are the prerequisites for Xenotransplantation?", "ground_truth": ["Gene Editing", "Genetic Ethics"], "concept_id": 439, "hop_depth": 1}
+{"id": "genetics_T2_192", "domain": "genetics", "type": "T2_dependency", "query": "What are the prerequisites for Hardy-Weinberg Equilibrium?", "ground_truth": ["Allele Frequency", "Genotype Frequency"], "concept_id": 192, "hop_depth": 1}
+{"id": "genetics_T2_86", "domain": "genetics", "type": "T2_dependency", "query": "What are the prerequisites for Variable Number Tandem Repeat?", "ground_truth": ["Minisatellite"], "concept_id": 86, "hop_depth": 1}
+{"id": "genetics_T2_195", "domain": "genetics", "type": "T2_dependency", "query": "What are the prerequisites for Natural Selection?", "ground_truth": ["Population Genetics"], "concept_id": 195, "hop_depth": 1}
+{"id": "genetics_T2_186", "domain": "genetics", "type": "T2_dependency", "query": "What are the prerequisites for Odds Ratio?", "ground_truth": ["Effect Size"], "concept_id": 186, "hop_depth": 1}
+{"id": "genetics_T2_110", "domain": "genetics", "type": "T2_dependency", "query": "What are the prerequisites for Chromosomal Rearrangement?", "ground_truth": ["Structural Variation", "Chromosomal Inversion", "Chromosomal Translocation"], "concept_id": 110, "hop_depth": 1}
+{"id": "genetics_T2_354", "domain": "genetics", "type": "T2_dependency", "query": "What are the prerequisites for Preimplantation Diagnosis?", "ground_truth": ["Prenatal Genetic Testing"], "concept_id": 354, "hop_depth": 1}
+{"id": "genetics_T2_140", "domain": "genetics", "type": "T2_dependency", "query": "What are the prerequisites for LOD Score Threshold?", "ground_truth": ["LOD Score"], "concept_id": 140, "hop_depth": 1}
+{"id": "genetics_T2_370", "domain": "genetics", "type": "T2_dependency", "query": "What are the prerequisites for Cancer Genetics?", "ground_truth": ["Human Genetics"], "concept_id": 370, "hop_depth": 1}
+{"id": "genetics_T2_360", "domain": "genetics", "type": "T2_dependency", "query": "What are the prerequisites for Presymptomatic Testing?", "ground_truth": ["Predictive Testing"], "concept_id": 360, "hop_depth": 1}
+{"id": "genetics_T2_341", "domain": "genetics", "type": "T2_dependency", "query": "What are the prerequisites for RNA-Seq Analysis?", "ground_truth": ["Next-Gen Sequencing", "Gene Expression"], "concept_id": 341, "hop_depth": 1}
+{"id": "genetics_T2_38", "domain": "genetics", "type": "T2_dependency", "query": "What are the prerequisites for P-Value Interpretation?", "ground_truth": ["Null Hypothesis in Genetics"], "concept_id": 38, "hop_depth": 1}
+{"id": "genetics_T2_321", "domain": "genetics", "type": "T2_dependency", "query": "What are the prerequisites for Variant Calling?", "ground_truth": ["Next-Gen Sequencing", "Sequence Alignment"], "concept_id": 321, "hop_depth": 1}
+{"id": "genetics_T2_90", "domain": "genetics", "type": "T2_dependency", "query": "What are the prerequisites for Tag SNP?", "ground_truth": ["Haplotype Block", "Linkage Disequilibrium"], "concept_id": 90, "hop_depth": 1}
+{"id": "genetics_T2_282", "domain": "genetics", "type": "T2_dependency", "query": "What are the prerequisites for C. Elegans Genetics?", "ground_truth": ["Model Organism"], "concept_id": 282, "hop_depth": 1}
+{"id": "genetics_T2_129", "domain": "genetics", "type": "T2_dependency", "query": "What are the prerequisites for Physical Map?", "ground_truth": ["Genetic Map", "Molecular Markers"], "concept_id": 129, "hop_depth": 1}
+{"id": "genetics_T2_243", "domain": "genetics", "type": "T2_dependency", "query": "What are the prerequisites for MicroRNA?", "ground_truth": ["Noncoding RNA"], "concept_id": 243, "hop_depth": 1}
+{"id": "genetics_T2_142", "domain": "genetics", "type": "T2_dependency", "query": "What are the prerequisites for Nonparametric Linkage?", "ground_truth": ["Linkage Analysis"], "concept_id": 142, "hop_depth": 1}
+{"id": "genetics_T3_211_229", "domain": "genetics", "type": "T3_path", "query": "What is the prerequisite chain from Gene Expression to Feedback Loop?", "ground_truth": ["Feedback Loop", "Network Motif", "Gene Regulatory Network", "Gene Expression"], "concept_id": 229, "hop_depth": 3, "path_ids": [229, 228, 227, 211]}
+{"id": "genetics_T3_266_444", "domain": "genetics", "type": "T3_path", "query": "What is the prerequisite chain from Forward Genetics to Research Ethics?", "ground_truth": ["Research Ethics", "Experimental Design", "Forward Genetics"], "concept_id": 444, "hop_depth": 2, "path_ids": [444, 441, 266]}
+{"id": "genetics_T3_111_154", "domain": "genetics", "type": "T3_path", "query": "What is the prerequisite chain from Linkage to Fine Structure Mapping?", "ground_truth": ["Fine Structure Mapping", "Intragenic Recombination", "Recombination", "Linkage"], "concept_id": 154, "hop_depth": 3, "path_ids": [154, 155, 113, 111]}
+{"id": "genetics_T3_111_150", "domain": "genetics", "type": "T3_path", "query": "What is the prerequisite chain from Linkage to Centromere Mapping?", "ground_truth": ["Centromere Mapping", "Ordered Tetrad", "Tetrad Analysis", "Recombination", "Linkage"], "concept_id": 150, "hop_depth": 4, "path_ids": [150, 148, 147, 113, 111]}
+{"id": "genetics_T3_189_386", "domain": "genetics", "type": "T3_path", "query": "What is the prerequisite chain from Population Genetics to Genetic Risk Factor?", "ground_truth": ["Genetic Risk Factor", "GWAS", "Population Genetics"], "concept_id": 386, "hop_depth": 2, "path_ids": [386, 179, 189]}
+{"id": "genetics_T3_51_102", "domain": "genetics", "type": "T3_path", "query": "What is the prerequisite chain from Genome Organization to Gene Family?", "ground_truth": ["Gene Family", "Gene Duplication", "Genome Organization"], "concept_id": 102, "hop_depth": 2, "path_ids": [102, 99, 51]}
+{"id": "genetics_T3_306_435", "domain": "genetics", "type": "T3_path", "query": "What is the prerequisite chain from Genomics to Microbiome Genetics?", "ground_truth": ["Microbiome Genetics", "Metagenomics", "Genomics"], "concept_id": 435, "hop_depth": 2, "path_ids": [435, 434, 306]}
+{"id": "genetics_T3_1_356", "domain": "genetics", "type": "T3_path", "query": "What is the prerequisite chain from Genetic Inference to Pedigree Construction?", "ground_truth": ["Pedigree Construction", "Pedigree Analysis", "Genetic Inference"], "concept_id": 356, "hop_depth": 2, "path_ids": [356, 8, 1]}
+{"id": "genetics_T3_51_437", "domain": "genetics", "type": "T3_path", "query": "What is the prerequisite chain from Genome Organization to 4D Nucleome?", "ground_truth": ["4D Nucleome", "Topologically Assoc Domain", "Chromatin State", "Chromatin", "Chromosome Structure", "Genome Organization"], "concept_id": 437, "hop_depth": 5, "path_ids": [437, 257, 251, 59, 52, 51]}
+{"id": "genetics_T3_211_245", "domain": "genetics", "type": "T3_path", "query": "What is the prerequisite chain from Gene Expression to Long Noncoding RNA?", "ground_truth": ["Long Noncoding RNA", "Noncoding RNA", "Gene Expression"], "concept_id": 245, "hop_depth": 2, "path_ids": [245, 246, 211]}
+{"id": "genetics_T3_51_150", "domain": "genetics", "type": "T3_path", "query": "What is the prerequisite chain from Genome Organization to Centromere Mapping?", "ground_truth": ["Centromere Mapping", "Centromere Structure", "Chromosome Structure", "Genome Organization"], "concept_id": 150, "hop_depth": 3, "path_ids": [150, 57, 52, 51]}
+{"id": "genetics_T3_51_369", "domain": "genetics", "type": "T3_path", "query": "What is the prerequisite chain from Genome Organization to Biomarker Discovery?", "ground_truth": ["Biomarker Discovery", "GWAS", "Single Nucleotide Polymorphism", "Genetic Variation", "Genome Organization"], "concept_id": 369, "hop_depth": 4, "path_ids": [369, 179, 74, 73, 51]}
+{"id": "genetics_T3_51_55", "domain": "genetics", "type": "T3_path", "query": "What is the prerequisite chain from Genome Organization to Constitutive Heterochromatin?", "ground_truth": ["Constitutive Heterochromatin", "Heterochromatin", "Chromosome Structure", "Genome Organization"], "concept_id": 55, "hop_depth": 3, "path_ids": [55, 54, 52, 51]}
+{"id": "genetics_T3_211_239", "domain": "genetics", "type": "T3_path", "query": "What is the prerequisite chain from Gene Expression to Exon Skipping?", "ground_truth": ["Exon Skipping", "Alternative Splicing", "RNA Splicing", "Post-Transcriptional Reg", "Gene Expression"], "concept_id": 239, "hop_depth": 4, "path_ids": [239, 238, 237, 236, 211]}
+{"id": "genetics_T3_51_150", "domain": "genetics", "type": "T3_path", "query": "What is the prerequisite chain from Genome Organization to Centromere Mapping?", "ground_truth": ["Centromere Mapping", "Centromere Structure", "Chromosome Structure", "Genome Organization"], "concept_id": 150, "hop_depth": 3, "path_ids": [150, 57, 52, 51]}
+{"id": "genetics_T3_306_427", "domain": "genetics", "type": "T3_path", "query": "What is the prerequisite chain from Genomics to Large Language Models Bio?", "ground_truth": ["Large Language Models Bio", "Deep Learning in Genomics", "AI in Genomics", "Genomics"], "concept_id": 427, "hop_depth": 3, "path_ids": [427, 426, 424, 306]}
+{"id": "genetics_T3_266_272", "domain": "genetics", "type": "T3_path", "query": "What is the prerequisite chain from Forward Genetics to Saturation Mutagenesis?", "ground_truth": ["Saturation Mutagenesis", "Mutagenesis Screen", "Forward Genetics"], "concept_id": 272, "hop_depth": 2, "path_ids": [272, 268, 266]}
+{"id": "genetics_T3_306_344", "domain": "genetics", "type": "T3_path", "query": "What is the prerequisite chain from Genomics to Pathway Enrichment?", "ground_truth": ["Pathway Enrichment", "Gene Ontology", "Genome Annotation", "Genomics"], "concept_id": 344, "hop_depth": 3, "path_ids": [344, 343, 319, 306]}
+{"id": "genetics_T3_156_174", "domain": "genetics", "type": "T3_path", "query": "What is the prerequisite chain from Quantitative Genetics to Heritability Estimation?", "ground_truth": ["Heritability Estimation", "Heritability", "Quantitative Genetics"], "concept_id": 174, "hop_depth": 2, "path_ids": [174, 162, 156]}
+{"id": "genetics_T3_346_382", "domain": "genetics", "type": "T3_path", "query": "What is the prerequisite chain from Human Genetics to Circulating Tumor DNA?", "ground_truth": ["Circulating Tumor DNA", "Liquid Biopsy", "Cancer Genetics", "Human Genetics"], "concept_id": 382, "hop_depth": 3, "path_ids": [382, 381, 370, 346]}
+{"id": "genetics_T3_51_431", "domain": "genetics", "type": "T3_path", "query": "What is the prerequisite chain from Genome Organization to Pangenome Reference?", "ground_truth": ["Pangenome Reference", "Pangenome", "Genetic Variation", "Genome Organization"], "concept_id": 431, "hop_depth": 3, "path_ids": [431, 430, 73, 51]}
+{"id": "genetics_T3_1_347", "domain": "genetics", "type": "T3_path", "query": "What is the prerequisite chain from Genetic Inference to Mendelian Disease?", "ground_truth": ["Mendelian Disease", "Pedigree Analysis", "Genetic Inference"], "concept_id": 347, "hop_depth": 2, "path_ids": [347, 8, 1]}
+{"id": "genetics_T3_111_154", "domain": "genetics", "type": "T3_path", "query": "What is the prerequisite chain from Linkage to Fine Structure Mapping?", "ground_truth": ["Fine Structure Mapping", "Intragenic Recombination", "Recombination", "Linkage"], "concept_id": 154, "hop_depth": 3, "path_ids": [154, 155, 113, 111]}
+{"id": "genetics_T3_1_194", "domain": "genetics", "type": "T3_path", "query": "What is the prerequisite chain from Genetic Inference to Chi-Square HWE Test?", "ground_truth": ["Chi-Square HWE Test", "Chi-Square Test", "Probability in Genetics", "Genetic Inference"], "concept_id": 194, "hop_depth": 3, "path_ids": [194, 33, 2, 1]}
+{"id": "genetics_T3_266_301", "domain": "genetics", "type": "T3_path", "query": "What is the prerequisite chain from Forward Genetics to GAL4-UAS System?", "ground_truth": ["GAL4-UAS System", "Transgenic Organism", "Gene Editing", "CRISPR-Cas9", "Reverse Genetics", "Forward Genetics"], "concept_id": 301, "hop_depth": 5, "path_ids": [301, 297, 291, 289, 267, 266]}
+{"id": "genetics_T4_FOUND", "domain": "genetics", "type": "T4_aggregate", "query": "List all FOUND concepts in this knowledge graph", "ground_truth": ["Genetic Inference", "Genome Organization", "Linkage", "Quantitative Genetics", "Population Genetics", "Gene Expression", "Stem Cell Gene Expression", "Forward Genetics", "Model Organism", "Functional Genomics", "Genomics", "Version Control in Genomics", "Human Genetics", "Pharmacogenomics", "Genetic Ethics", "Diversity in Genomics", "Single-Cell Genomics", "AI in Genomics", "Deep Learning in Genomics", "Long-Read Genomics", "Metagenomics", "Synthetic Genomics"], "taxonomy_id": "FOUND", "hop_depth": 0}
+{"id": "genetics_T4_PROB", "domain": "genetics", "type": "T4_aggregate", "query": "List all PROB concepts in this knowledge graph", "ground_truth": ["Probability in Genetics", "Conditional Probability", "Bayesian Reasoning", "Prior Probability", "Posterior Probability", "Likelihood Ratio", "Chi-Square Test", "Goodness of Fit Test", "Null Hypothesis in Genetics", "P-Value Interpretation"], "taxonomy_id": "PROB", "hop_depth": 0}
+{"id": "genetics_T4_PED", "domain": "genetics", "type": "T4_aggregate", "query": "List all PED concepts in this knowledge graph", "ground_truth": ["Pedigree Analysis", "Autosomal Dominant Pedigree", "Autosomal Recessive Pedigree", "X-Linked Inheritance", "X-Linked Recessive Pedigree", "X-Linked Dominant Pedigree", "Carrier Probability", "Penetrance", "Incomplete Penetrance", "Expressivity", "Variable Expressivity", "Phenocopy", "Genetic Heterogeneity", "Locus Heterogeneity", "Allelic Heterogeneity", "Epistasis", "Duplicate Epistasis", "Complementary Epistasis", "Suppressor Epistasis", "Epistatic Pathway Analysis", "Complementation Test", "Complementation Group", "Cis-Trans Test", "Allelism", "Functional Allelism", "Test Cross", "Reciprocal Cross", "Modified Mendelian Ratios", "Lethal Alleles", "Pleiotropy", "Genetic Background Effects", "Age of Onset", "Anticipation", "Genomic Imprinting", "Parent of Origin Effects", "Uniparental Disomy", "Mosaicism", "Somatic Mosaicism", "Germline Mosaicism", "Pedigree Construction"], "taxonomy_id": "PED", "hop_depth": 0}
+{"id": "genetics_T4_GSTR", "domain": "genetics", "type": "T4_aggregate", "query": "List all GSTR concepts in this knowledge graph", "ground_truth": ["Chromosome Structure", "Euchromatin", "Heterochromatin", "Constitutive Heterochromatin", "Facultative Heterochromatin", "Centromere Structure", "Telomere Structure", "Chromatin", "Nucleosome", "Histone Proteins", "Histone Modifications", "Histone Acetylation", "Histone Methylation", "Chromatin Remodeling", "Epigenetics", "DNA Methylation", "CpG Islands", "Epigenetic Inheritance", "X-Inactivation", "Dosage Compensation", "Barr Body", "Open Chromatin", "Closed Chromatin", "Bivalent Chromatin", "Poised Enhancer", "Super Enhancer", "Topologically Assoc Domain", "Chromatin Looping"], "taxonomy_id": "GSTR", "hop_depth": 0}
+{"id": "genetics_T4_GVAR", "domain": "genetics", "type": "T4_aggregate", "query": "List all GVAR concepts in this knowledge graph", "ground_truth": ["Genetic Variation", "Single Nucleotide Polymorphism", "Insertion Deletion Variant", "Copy Number Variation", "Structural Variation", "Chromosomal Inversion", "Chromosomal Translocation", "Chromosomal Deletion", "Chromosomal Duplication", "Tandem Repeat", "Short Tandem Repeat", "Microsatellite", "Minisatellite", "Variable Number Tandem Repeat", "Haplotype", "Haplotype Block", "Linkage Disequilibrium", "Tag SNP", "HapMap Project", "Transposable Elements", "DNA Transposon", "Retrotransposon", "LINE Element", "SINE Element", "Alu Element", "Transposon Mutagenesis", "Gene Duplication", "Paralog", "Ortholog", "Gene Family", "Pseudogene", "Segmental Duplication", "Polyploidy", "Aneuploidy", "Trisomy", "Monosomy", "Nondisjunction", "Chromosomal Rearrangement"], "taxonomy_id": "GVAR", "hop_depth": 0}
+{"id": "genetics_T4_MAP", "domain": "genetics", "type": "T4_aggregate", "query": "List all MAP concepts in this knowledge graph", "ground_truth": ["Genetic Linkage", "Recombination", "Crossing Over", "Recombination Frequency", "Genetic Map", "Map Distance", "Centimorgan", "Two-Point Cross", "Three-Point Cross", "Interference", "Coefficient of Coincidence", "Gene Order Determination", "Genetic Markers", "Molecular Markers", "Restriction Fragment Length", "Microsatellite Markers", "SNP Markers", "Physical Map", "Cytogenetic Map", "Radiation Hybrid Mapping", "Somatic Cell Hybridization", "Synteny", "Comparative Genomics", "Gene Discovery Strategies", "Positional Cloning", "Candidate Gene Approach", "Linkage Analysis", "LOD Score", "LOD Score Threshold", "Parametric Linkage", "Nonparametric Linkage", "Recombination Hotspots", "Sex Differences in Mapping", "Mitotic Recombination", "Gene Conversion", "Tetrad Analysis", "Ordered Tetrad", "Unordered Tetrad", "Centromere Mapping", "Half-Tetrad Analysis", "Deletion Mapping", "Complementation Mapping", "Fine Structure Mapping", "Intragenic Recombination", "RNA Interference", "RNA Interference Screen"], "taxonomy_id": "MAP", "hop_depth": 0}
+{"id": "genetics_T4_QUANT", "domain": "genetics", "type": "T4_aggregate", "query": "List all QUANT concepts in this knowledge graph", "ground_truth": ["Quantitative Trait", "Continuous Variation", "Polygenic Inheritance", "Multifactorial Trait", "Threshold Trait", "Heritability", "Broad Sense Heritability", "Narrow Sense Heritability", "Additive Genetic Variance", "Dominance Variance", "Epistatic Variance", "Environmental Variance", "Phenotypic Variance", "Twin Studies", "Monozygotic Twins", "Dizygotic Twins", "Concordance Rate", "Heritability Estimation", "Quantitative Trait Locus", "QTL Mapping", "Interval Mapping", "Marker Assisted Selection", "GWAS", "Manhattan Plot", "Significance Threshold", "Multiple Testing Correction", "Bonferroni Correction", "False Discovery Rate", "Effect Size", "Odds Ratio", "Polygenic Risk Score", "Missing Heritability"], "taxonomy_id": "QUANT", "hop_depth": 0}
+{"id": "genetics_T4_POP", "domain": "genetics", "type": "T4_aggregate", "query": "List all POP concepts in this knowledge graph", "ground_truth": ["Allele Frequency", "Genotype Frequency", "Hardy-Weinberg Equilibrium", "Hardy-Weinberg Assumptions", "Chi-Square HWE Test", "Natural Selection", "Fitness", "Selection Coefficient", "Directional Selection", "Stabilizing Selection", "Disruptive Selection", "Balancing Selection", "Heterozygote Advantage", "Genetic Drift", "Bottleneck Effect", "Founder Effect", "Gene Flow", "Migration", "Mutation Rate", "Population Structure", "Fixation Index"], "taxonomy_id": "POP", "hop_depth": 0}
+{"id": "genetics_T4_REG", "domain": "genetics", "type": "T4_aggregate", "query": "List all REG concepts in this knowledge graph", "ground_truth": ["Transcription Regulation", "Promoter", "TATA Box", "Transcription Factor", "General Transcription Factor", "Specific Transcription Factor", "Activator", "Repressor", "Enhancer", "Silencer", "Insulator", "Cis-Regulatory Element", "Trans-Acting Factor", "Transcriptional Logic", "Combinatorial Control", "Gene Regulatory Network", "Network Motif", "Feedback Loop", "Feed-Forward Loop", "Operon Model", "Lac Operon", "Trp Operon", "Positive Regulation", "Negative Regulation", "Post-Transcriptional Reg", "RNA Splicing", "Alternative Splicing", "Exon Skipping", "RNA Editing", "mRNA Stability", "MicroRNA", "Small Interfering RNA", "Long Noncoding RNA", "Noncoding RNA", "Riboswitch", "Translational Regulation", "Protein Degradation", "Ubiquitin Pathway", "Chromatin State", "Cell Identity", "Cell Fate Determination", "Master Regulator Gene", "Pioneer Factor", "Differentiation", "Cellular Reprogramming"], "taxonomy_id": "REG", "hop_depth": 0}
+{"id": "genetics_T4_EXP", "domain": "genetics", "type": "T4_aggregate", "query": "List all EXP concepts in this knowledge graph", "ground_truth": ["Reverse Genetics", "Mutagenesis Screen", "Chemical Mutagenesis", "EMS Mutagenesis", "Insertional Mutagenesis", "Saturation Mutagenesis", "Enhancer Trap", "Suppressor Screen", "Modifier Screen", "Genetic Mosaic Analysis", "Clonal Analysis", "Drosophila Genetics", "Yeast Genetics", "Mouse Genetics", "C. Elegans Genetics", "Zebrafish Genetics", "Arabidopsis Genetics", "Gene Knockout", "Conditional Knockout", "Knockdown", "CRISPR-Cas9", "Guide RNA Design", "Gene Editing", "Homology Directed Repair", "NHEJ Repair", "Base Editing", "Prime Editing", "Gene Drive", "Transgenic Organism", "Reporter Gene", "GFP Reporter", "Cre-Lox System", "GAL4-UAS System", "Phenotype Scoring", "Genetic Interaction", "Synthetic Lethality", "Somatic Gene Editing", "Experimental Design", "Hypothesis Testing"], "taxonomy_id": "EXP", "hop_depth": 0}
+{"id": "genetics_T4_BIOINFO", "domain": "genetics", "type": "T4_aggregate", "query": "List all BIOINFO concepts in this knowledge graph", "ground_truth": ["Genome Sequencing", "Sanger Sequencing", "Next-Gen Sequencing", "Illumina Sequencing", "Long-Read Sequencing", "Whole Genome Sequencing", "Whole Exome Sequencing", "Targeted Sequencing", "Sequence Alignment", "BLAST Algorithm", "Pairwise Alignment", "Multiple Sequence Alignment", "Genome Annotation", "Gene Prediction", "Variant Calling", "VCF File Format", "FASTA File Format", "FASTQ File Format", "BAM File Format", "BED File Format", "Variant Annotation", "Variant Classification", "Benign Variant", "Pathogenic Variant", "Variant of Uncertain Sig", "Genomic Databases", "NCBI Database", "Ensembl Database", "UCSC Genome Browser", "ClinVar Database", "dbSNP Database", "Reproducible Workflows", "Pipeline Automation", "RNA-Seq Analysis", "Differential Expression", "Gene Ontology", "Pathway Enrichment", "Functional Annotation", "Data Interpretation", "Computational Workflow"], "taxonomy_id": "BIOINFO", "hop_depth": 0}
+{"id": "genetics_T4_CLIN", "domain": "genetics", "type": "T4_aggregate", "query": "List all CLIN concepts in this knowledge graph", "ground_truth": ["Mendelian Disease", "Complex Disease", "Genetic Counseling", "Risk Assessment", "Carrier Screening", "Newborn Screening", "Prenatal Genetic Testing", "Preimplantation Diagnosis", "Family History Assessment", "Genetic Testing Types", "Diagnostic Testing", "Predictive Testing", "Presymptomatic Testing", "Drug Metabolism Variation", "CYP450 Polymorphisms", "Dosage Optimization", "Adverse Drug Reaction", "Companion Diagnostics", "Precision Medicine", "Targeted Therapy", "Biomarker Discovery", "Cancer Genetics", "Oncogene", "Tumor Suppressor Gene", "Two-Hit Hypothesis", "Somatic Mutation in Cancer", "Driver Mutation", "Passenger Mutation", "Tumor Mutational Burden", "Microsatellite Instability", "Lynch Syndrome", "BRCA Genes", "Liquid Biopsy", "Circulating Tumor DNA", "Hereditary Cancer Syndrome", "Chromosomal Instability", "Cancer Predisposition", "Genetic Risk Factor", "Polygenic Disease Risk", "Gene Therapy", "Antisense Therapy", "Gene Replacement Therapy", "Variant Interpretation", "Genotype-Phenotype Models", "Systems Genetics"], "taxonomy_id": "CLIN", "hop_depth": 0}
+{"id": "genetics_T4_ETHICS", "domain": "genetics", "type": "T4_aggregate", "query": "List all ETHICS concepts in this knowledge graph", "ground_truth": ["Informed Consent", "Genetic Privacy", "Genetic Discrimination", "GINA Legislation", "Data Ownership", "Biobank Ethics", "Return of Results", "Incidental Findings", "Duty to Warn", "Equity in Genomic Medicine", "Health Disparities", "Reference Genome Bias", "Ancestry and Identity", "Gene Editing Ethics", "Germline Editing Debate", "Enhancement vs Therapy", "Eugenics History", "DTC Genetic Testing", "DTC Testing Regulation", "Genetic Literacy", "Public Engagement", "Science Communication", "Research Ethics", "Scientific Communication"], "taxonomy_id": "ETHICS", "hop_depth": 0}
+{"id": "genetics_T4_FRONT", "domain": "genetics", "type": "T4_aggregate", "query": "List all FRONT concepts in this knowledge graph", "ground_truth": ["CRISPR Advancements", "CRISPR Therapeutics", "In Vivo Gene Editing", "Epigenome Editing", "Single-Cell RNA Sequencing", "Spatial Transcriptomics", "Cell Atlas Projects", "Machine Learning Variants", "Large Language Models Bio", "Protein Structure AI", "Pangenome", "Pangenome Reference", "Structural Variant Calling", "Telomere-to-Telomere", "Microbiome Genetics", "Gene Regulation Atlas", "4D Nucleome", "Xenotransplantation", "Emerging Research Methods", "Capstone Genomic Project"], "taxonomy_id": "FRONT", "hop_depth": 0}
+{"id": "genetics_T5_8_2", "domain": "genetics", "type": "T5_cross_concept", "query": "How does Pedigree Analysis relate to Probability in Genetics?", "ground_truth": ["Pedigree Analysis", "Probability in Genetics", "Genetic Inference"], "concept_id_a": 8, "concept_id_b": 2, "hop_depth": 1}
+{"id": "genetics_T5_90_89", "domain": "genetics", "type": "T5_cross_concept", "query": "How does Tag SNP relate to Linkage Disequilibrium?", "ground_truth": ["Tag SNP", "Linkage Disequilibrium"], "concept_id_a": 90, "concept_id_b": 89, "hop_depth": 1}
+{"id": "genetics_T5_65_62", "domain": "genetics", "type": "T5_cross_concept", "query": "How does Chromatin Remodeling relate to Histone Modifications?", "ground_truth": ["Chromatin Remodeling", "Histone Modifications"], "concept_id_a": 65, "concept_id_b": 62, "hop_depth": 1}
+{"id": "genetics_T5_116_115", "domain": "genetics", "type": "T5_cross_concept", "query": "How does Genetic Map relate to Recombination Frequency?", "ground_truth": ["Genetic Map", "Recombination Frequency"], "concept_id_a": 116, "concept_id_b": 115, "hop_depth": 1}
+{"id": "genetics_T5_417_416", "domain": "genetics", "type": "T5_cross_concept", "query": "How does CRISPR Therapeutics relate to CRISPR Advancements?", "ground_truth": ["CRISPR Therapeutics", "CRISPR Advancements"], "concept_id_a": 417, "concept_id_b": 416, "hop_depth": 1}
+{"id": "genetics_T5_30_28", "domain": "genetics", "type": "T5_cross_concept", "query": "How does Cis-Trans Test relate to Complementation Test?", "ground_truth": ["Cis-Trans Test", "Complementation Test"], "concept_id_a": 30, "concept_id_b": 28, "hop_depth": 1}
+{"id": "genetics_T5_283_278", "domain": "genetics", "type": "T5_cross_concept", "query": "How does Zebrafish Genetics relate to Model Organism?", "ground_truth": ["Zebrafish Genetics", "Model Organism"], "concept_id_a": 283, "concept_id_b": 278, "hop_depth": 1}
+{"id": "genetics_T5_442_441", "domain": "genetics", "type": "T5_cross_concept", "query": "How does Hypothesis Testing relate to Experimental Design?", "ground_truth": ["Hypothesis Testing", "Experimental Design"], "concept_id_a": 442, "concept_id_b": 441, "hop_depth": 1}
+{"id": "genetics_T5_421_341", "domain": "genetics", "type": "T5_cross_concept", "query": "How does Single-Cell RNA Sequencing relate to RNA-Seq Analysis?", "ground_truth": ["Single-Cell RNA Sequencing", "RNA-Seq Analysis"], "concept_id_a": 421, "concept_id_b": 341, "hop_depth": 1}
+{"id": "genetics_T5_115_114", "domain": "genetics", "type": "T5_cross_concept", "query": "How does Recombination Frequency relate to Crossing Over?", "ground_truth": ["Recombination Frequency", "Crossing Over", "Recombination"], "concept_id_a": 115, "concept_id_b": 114, "hop_depth": 1}
+{"id": "genetics_T5_335_332", "domain": "genetics", "type": "T5_cross_concept", "query": "How does UCSC Genome Browser relate to Genomic Databases?", "ground_truth": ["UCSC Genome Browser", "Genomic Databases"], "concept_id_a": 335, "concept_id_b": 332, "hop_depth": 1}
+{"id": "genetics_T5_101_134", "domain": "genetics", "type": "T5_cross_concept", "query": "How does Ortholog relate to Comparative Genomics?", "ground_truth": ["Ortholog", "Comparative Genomics"], "concept_id_a": 101, "concept_id_b": 134, "hop_depth": 1}
+{"id": "genetics_T5_35_1", "domain": "genetics", "type": "T5_cross_concept", "query": "How does Test Cross relate to Genetic Inference?", "ground_truth": ["Test Cross", "Genetic Inference"], "concept_id_a": 35, "concept_id_b": 1, "hop_depth": 1}
+{"id": "genetics_T5_235_219", "domain": "genetics", "type": "T5_cross_concept", "query": "How does Negative Regulation relate to Repressor?", "ground_truth": ["Negative Regulation", "Repressor"], "concept_id_a": 235, "concept_id_b": 219, "hop_depth": 1}
+{"id": "genetics_T5_277_276", "domain": "genetics", "type": "T5_cross_concept", "query": "How does Clonal Analysis relate to Genetic Mosaic Analysis?", "ground_truth": ["Clonal Analysis", "Genetic Mosaic Analysis"], "concept_id_a": 277, "concept_id_b": 276, "hop_depth": 1}
+{"id": "genetics_T5_33_2", "domain": "genetics", "type": "T5_cross_concept", "query": "How does Chi-Square Test relate to Probability in Genetics?", "ground_truth": ["Chi-Square Test", "Probability in Genetics"], "concept_id_a": 33, "concept_id_b": 2, "hop_depth": 1}
+{"id": "genetics_T5_273_271", "domain": "genetics", "type": "T5_cross_concept", "query": "How does Enhancer Trap relate to Insertional Mutagenesis?", "ground_truth": ["Enhancer Trap", "Insertional Mutagenesis"], "concept_id_a": 273, "concept_id_b": 271, "hop_depth": 1}
+{"id": "genetics_T5_161_160", "domain": "genetics", "type": "T5_cross_concept", "query": "How does Threshold Trait relate to Multifactorial Trait?", "ground_truth": ["Threshold Trait", "Multifactorial Trait"], "concept_id_a": 161, "concept_id_b": 160, "hop_depth": 1}
+{"id": "genetics_T5_187_185", "domain": "genetics", "type": "T5_cross_concept", "query": "How does Polygenic Risk Score relate to Effect Size?", "ground_truth": ["Polygenic Risk Score", "Effect Size", "GWAS"], "concept_id_a": 187, "concept_id_b": 185, "hop_depth": 1}
+{"id": "genetics_T5_84_83", "domain": "genetics", "type": "T5_cross_concept", "query": "How does Microsatellite relate to Short Tandem Repeat?", "ground_truth": ["Microsatellite", "Short Tandem Repeat"], "concept_id_a": 84, "concept_id_b": 83, "hop_depth": 1}
+{"id": "genetics_T5_270_269", "domain": "genetics", "type": "T5_cross_concept", "query": "How does EMS Mutagenesis relate to Chemical Mutagenesis?", "ground_truth": ["EMS Mutagenesis", "Chemical Mutagenesis"], "concept_id_a": 270, "concept_id_b": 269, "hop_depth": 1}
+{"id": "genetics_T5_427_426", "domain": "genetics", "type": "T5_cross_concept", "query": "How does Large Language Models Bio relate to Deep Learning in Genomics?", "ground_truth": ["Large Language Models Bio", "Deep Learning in Genomics"], "concept_id_a": 427, "concept_id_b": 426, "hop_depth": 1}
+{"id": "genetics_T5_315_306", "domain": "genetics", "type": "T5_cross_concept", "query": "How does Sequence Alignment relate to Genomics?", "ground_truth": ["Sequence Alignment", "Genomics"], "concept_id_a": 315, "concept_id_b": 306, "hop_depth": 1}
+{"id": "genetics_T5_121_120", "domain": "genetics", "type": "T5_cross_concept", "query": "How does Interference relate to Three-Point Cross?", "ground_truth": ["Interference", "Three-Point Cross"], "concept_id_a": 121, "concept_id_b": 120, "hop_depth": 1}
+{"id": "genetics_T5_178_175", "domain": "genetics", "type": "T5_cross_concept", "query": "How does Marker Assisted Selection relate to Quantitative Trait Locus?", "ground_truth": ["Marker Assisted Selection", "Quantitative Trait Locus"], "concept_id_a": 178, "concept_id_b": 175, "hop_depth": 1}
+{"id": "genetics_T5_127_125", "domain": "genetics", "type": "T5_cross_concept", "query": "How does Microsatellite Markers relate to Molecular Markers?", "ground_truth": ["Microsatellite Markers", "Molecular Markers"], "concept_id_a": 127, "concept_id_b": 125, "hop_depth": 1}
+{"id": "genetics_T5_136_135", "domain": "genetics", "type": "T5_cross_concept", "query": "How does Positional Cloning relate to Gene Discovery Strategies?", "ground_truth": ["Positional Cloning", "Gene Discovery Strategies"], "concept_id_a": 136, "concept_id_b": 135, "hop_depth": 1}
+{"id": "genetics_T5_320_319", "domain": "genetics", "type": "T5_cross_concept", "query": "How does Gene Prediction relate to Genome Annotation?", "ground_truth": ["Gene Prediction", "Genome Annotation"], "concept_id_a": 320, "concept_id_b": 319, "hop_depth": 1}
+{"id": "genetics_T5_21_20", "domain": "genetics", "type": "T5_cross_concept", "query": "How does Locus Heterogeneity relate to Genetic Heterogeneity?", "ground_truth": ["Locus Heterogeneity", "Genetic Heterogeneity"], "concept_id_a": 21, "concept_id_b": 20, "hop_depth": 1}
+{"id": "genetics_T5_137_135", "domain": "genetics", "type": "T5_cross_concept", "query": "How does Candidate Gene Approach relate to Gene Discovery Strategies?", "ground_truth": ["Candidate Gene Approach", "Gene Discovery Strategies"], "concept_id_a": 137, "concept_id_b": 135, "hop_depth": 1}
+{"id": "genetics_T5_255_220", "domain": "genetics", "type": "T5_cross_concept", "query": "How does Poised Enhancer relate to Enhancer?", "ground_truth": ["Poised Enhancer", "Enhancer"], "concept_id_a": 255, "concept_id_b": 220, "hop_depth": 1}
+{"id": "genetics_T5_319_315", "domain": "genetics", "type": "T5_cross_concept", "query": "How does Genome Annotation relate to Sequence Alignment?", "ground_truth": ["Genome Annotation", "Sequence Alignment", "Genomics"], "concept_id_a": 319, "concept_id_b": 315, "hop_depth": 1}
+{"id": "genetics_T5_187_179", "domain": "genetics", "type": "T5_cross_concept", "query": "How does Polygenic Risk Score relate to GWAS?", "ground_truth": ["Polygenic Risk Score", "GWAS"], "concept_id_a": 187, "concept_id_b": 179, "hop_depth": 1}
+{"id": "genetics_T5_203_189", "domain": "genetics", "type": "T5_cross_concept", "query": "How does Genetic Drift relate to Population Genetics?", "ground_truth": ["Genetic Drift", "Population Genetics"], "concept_id_a": 203, "concept_id_b": 189, "hop_depth": 1}
+{"id": "genetics_T5_125_124", "domain": "genetics", "type": "T5_cross_concept", "query": "How does Molecular Markers relate to Genetic Markers?", "ground_truth": ["Molecular Markers", "Genetic Markers"], "concept_id_a": 125, "concept_id_b": 124, "hop_depth": 1}
+{"id": "genetics_T5_88_89", "domain": "genetics", "type": "T5_cross_concept", "query": "How does Haplotype Block relate to Linkage Disequilibrium?", "ground_truth": ["Haplotype Block", "Linkage Disequilibrium", "Haplotype"], "concept_id_a": 88, "concept_id_b": 89, "hop_depth": 1}
+{"id": "genetics_T5_295_289", "domain": "genetics", "type": "T5_cross_concept", "query": "How does Prime Editing relate to CRISPR-Cas9?", "ground_truth": ["Prime Editing", "CRISPR-Cas9"], "concept_id_a": 295, "concept_id_b": 289, "hop_depth": 1}
+{"id": "genetics_T5_32_31", "domain": "genetics", "type": "T5_cross_concept", "query": "How does Functional Allelism relate to Allelism?", "ground_truth": ["Functional Allelism", "Allelism"], "concept_id_a": 32, "concept_id_b": 31, "hop_depth": 1}