\section{Database Schema} \label{app:schema} NegBioDB uses three separate SQLite databases, one per domain, sharing common design patterns: WAL journal mode, foreign key enforcement, COALESCE-based deduplication indexes, and a four-tier confidence system (gold/silver/bronze/copper). Full DDL for all migrations is available in the repository. Below we summarize the key tables. \subsection{DTI Domain Schema} Two migrations: \texttt{001\_initial\_schema} (core tables) and \texttt{002\_target\_variants} (variant support). \begin{small} \begin{verbatim} -- Core entity tables compounds (compound_id PK, canonical_smiles, inchikey UNIQUE, inchikey_connectivity, pubchem_cid, chembl_id, molecular_weight, logp, hbd, hba, tpsa, qed, ...) targets (target_id PK, uniprot_accession UNIQUE, chembl_target_id, gene_symbol, target_family, development_level CHECK IN (Tclin/Tchem/Tbio/Tdark), ...) assays (assay_id PK, source_db, source_assay_id, assay_format CHECK IN (biochemical/cell-based/in_vivo), screen_type, z_factor, pubmed_id, ...) -- Core fact table (30.5M rows) negative_results (result_id PK, compound_id FK, target_id FK, assay_id FK, result_type CHECK IN (hard_negative/conditional_negative/ methodological_negative/dose_time_negative/ hypothesis_negative), confidence_tier CHECK IN (gold/silver/bronze/copper), activity_type, activity_value, pchembl_value, source_db, source_record_id, extraction_method, ...) -- Dedup: UNIQUE(compound_id, target_id, COALESCE(assay_id,-1), -- source_db, source_record_id) -- Aggregation (for ML export) compound_target_pairs (pair_id PK, compound_id FK, target_id FK, num_assays, num_sources, best_confidence, compound_degree, target_degree, ...) -- Variant support (migration 002) target_variants (variant_id PK, target_id FK, variant_label, source_db, UNIQUE(target_id, variant_label, ...)) \end{verbatim} \end{small} \subsection{CT Domain Schema} Two migrations: \texttt{001\_ct\_initial\_schema} (core tables) and \texttt{002\_schema\_fixes} (expert review fixes). \begin{small} \begin{verbatim} -- Entity tables interventions (intervention_id PK, intervention_type CHECK IN (drug/biologic/device/...), intervention_name, chembl_id, canonical_smiles, inchikey, molecular_type, ...) conditions (condition_id PK, condition_name, mesh_id, icd10_code, therapeutic_area, ...) clinical_trials (trial_id PK, source_trial_id UNIQUE, overall_status, trial_phase, enrollment_actual, primary_endpoint, why_stopped, termination_type CHECK IN (clinical_failure/ administrative/external_event/unknown), ...) -- Core fact table (132,925 rows) trial_failure_results (result_id PK, intervention_id FK, condition_id FK, trial_id FK, failure_category CHECK IN (efficacy/safety/pharmacokinetic/ enrollment/strategic/regulatory/design/other), confidence_tier CHECK IN (gold/silver/bronze/copper), p_value_primary, effect_size, serious_adverse_events, highest_phase_reached, result_interpretation CHECK IN (definitive_negative/inconclusive_underpowered/ mixed_endpoints/futility_stopped/safety_stopped/ administrative), source_db, extraction_method, ...) -- Dedup: UNIQUE(intervention_id, condition_id, -- COALESCE(trial_id,-1), source_db, source_record_id) -- Junction tables trial_interventions (trial_id FK, intervention_id FK, arm_role) trial_conditions (trial_id FK, condition_id FK) intervention_targets (intervention_id FK, uniprot_accession, ...) \end{verbatim} \end{small} \subsection{PPI Domain Schema} Two migrations: \texttt{001\_ppi\_initial\_schema} (core tables) and \texttt{002\_llm\_annotations} (protein annotations for LLM benchmark). \begin{small} \begin{verbatim} -- Entity table proteins (protein_id PK, uniprot_accession UNIQUE, gene_symbol, amino_acid_sequence, sequence_length, subcellular_location, function_description, go_terms, domain_annotations, ...) -- migration 002 -- Core fact table (2.23M rows) ppi_negative_results (result_id PK, protein1_id FK, protein2_id FK, experiment_id FK, evidence_type CHECK IN (experimental_non_interaction/ ml_predicted_negative/low_score_negative/ compartment_separated/literature_reported), confidence_tier CHECK IN (gold/silver/bronze/copper), interaction_score, detection_method, source_db, extraction_method, ..., CHECK (protein1_id < protein2_id)) -- canonical ordering -- Dedup: UNIQUE(protein1_id, protein2_id, -- COALESCE(experiment_id,-1), -- source_db, source_record_id) -- Aggregation protein_protein_pairs (pair_id PK, protein1_id FK, protein2_id FK, num_experiments, num_sources, best_confidence, protein1_degree, protein2_degree, ..., CHECK (protein1_id < protein2_id)) -- LLM support (migration 002) ppi_publication_abstracts (pmid PK, title, abstract, ...) \end{verbatim} \end{small} \subsection{Common Design Patterns} \begin{itemize}[nosep,leftmargin=*] \item \textbf{Deduplication:} All fact tables use \texttt{COALESCE(fk, -1)} in UNIQUE indexes to handle NULL foreign keys (SQLite treats NULLs as distinct in UNIQUE constraints). \item \textbf{Confidence tiers:} Four-level system across all domains: gold (systematic screens, multiple confirmations) $>$ silver (ML-derived, p-value based) $>$ bronze (computational, NLP-detected) $>$ copper (label-only). \item \textbf{Aggregation tables:} Pre-computed pair-level statistics for ML export, avoiding expensive JOINs during dataset construction. \item \textbf{Symmetric pairs (PPI):} \texttt{CHECK (protein1\_id $<$ protein2\_id)} enforces canonical ordering, preventing duplicate pair representations. \item \textbf{Schema migrations:} All databases track applied migrations in a \texttt{schema\_migrations} table for reproducible upgrades. \end{itemize}