Commit ·
35406a1
1
Parent(s): 8207e5a
Upload ncbi_disease.py
Browse files- ncbi_disease.py +148 -0
ncbi_disease.py
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# coding=utf-8
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# Copyright 2020 HuggingFace Datasets Authors.
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#
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# Licensed under the Apache License, Version 2.0 (the "License");
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# you may not use this file except in compliance with the License.
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# You may obtain a copy of the License at
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#
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# http://www.apache.org/licenses/LICENSE-2.0
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#
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# Unless required by applicable law or agreed to in writing, software
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# distributed under the License is distributed on an "AS IS" BASIS,
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# WITHOUT WARRANTIES OR CONDITIONS OF ANY KIND, either express or implied.
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# See the License for the specific language governing permissions and
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# limitations under the License.
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# Lint as: python3
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"""NCBI disease corpus: a resource for disease name recognition and concept normalization"""
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import datasets
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logger = datasets.logging.get_logger(__name__)
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_CITATION = """\
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@article{dougan2014ncbi,
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title={NCBI disease corpus: a resource for disease name recognition and concept normalization},
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author={Dogan, Rezarta Islamaj and Leaman, Robert and Lu, Zhiyong},
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journal={Journal of biomedical informatics},
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volume={47},
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pages={1--10},
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year={2014},
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publisher={Elsevier}
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}
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"""
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_DESCRIPTION = """\
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This paper presents the disease name and concept annotations of the NCBI disease corpus, a collection of 793 PubMed
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abstracts fully annotated at the mention and concept level to serve as a research resource for the biomedical natural
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language processing community. Each PubMed abstract was manually annotated by two annotators with disease mentions
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and their corresponding concepts in Medical Subject Headings (MeSH®) or Online Mendelian Inheritance in Man (OMIM®).
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Manual curation was performed using PubTator, which allowed the use of pre-annotations as a pre-step to manual annotations.
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Fourteen annotators were randomly paired and differing annotations were discussed for reaching a consensus in two
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annotation phases. In this setting, a high inter-annotator agreement was observed. Finally, all results were checked
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against annotations of the rest of the corpus to assure corpus-wide consistency.
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For more details, see: https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3951655/
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The original dataset can be downloaded from: https://www.ncbi.nlm.nih.gov/CBBresearch/Dogan/DISEASE/NCBI_corpus.zip
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This dataset has been converted to CoNLL format for NER using the following tool: https://github.com/spyysalo/standoff2conll
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Note: there is a duplicate document (PMID 8528200) in the original data, and the duplicate is recreated in the converted data.
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"""
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_HOMEPAGE = "https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3951655/"
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_URL = "https://github.com/spyysalo/ncbi-disease/raw/master/conll/"
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_TRAINING_FILE = "train.tsv"
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_DEV_FILE = "devel.tsv"
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_TEST_FILE = "test.tsv"
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class NCBIDiseaseConfig(datasets.BuilderConfig):
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"""BuilderConfig for NCBIDisease"""
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def __init__(self, **kwargs):
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"""BuilderConfig for NCBIDisease.
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Args:
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**kwargs: keyword arguments forwarded to super.
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"""
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super(NCBIDiseaseConfig, self).__init__(**kwargs)
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class NCBIDisease(datasets.GeneratorBasedBuilder):
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"""NCBIDisease dataset."""
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BUILDER_CONFIGS = [
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NCBIDiseaseConfig(name="ncbi_disease", version=datasets.Version("1.0.0"), description="NCBIDisease dataset"),
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]
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def _info(self):
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custom_names = ['O','B-GENE','I-GENE','B-CHEMICAL','I-CHEMICAL','B-DISEASE','I-DISEASE',
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'B-DNA', 'I-DNA', 'B-RNA', 'I-RNA', 'B-CELL_LINE', 'I-CELL_LINE', 'B-CELL_TYPE', 'I-CELL_TYPE',
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'B-PROTEIN', 'I-PROTEIN', 'B-SPECIES', 'I-SPECIES']
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return datasets.DatasetInfo(
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description=_DESCRIPTION,
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features=datasets.Features(
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{
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"id": datasets.Value("string"),
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"tokens": datasets.Sequence(datasets.Value("string")),
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"ner_tags": datasets.Sequence(
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datasets.features.ClassLabel(
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names=custom_names
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)
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),
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}
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),
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supervised_keys=None,
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homepage=_HOMEPAGE,
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citation=_CITATION,
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)
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def _split_generators(self, dl_manager):
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"""Returns SplitGenerators."""
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urls_to_download = {
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"train": f"{_URL}{_TRAINING_FILE}",
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"dev": f"{_URL}{_DEV_FILE}",
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"test": f"{_URL}{_TEST_FILE}",
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}
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downloaded_files = dl_manager.download_and_extract(urls_to_download)
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return [
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datasets.SplitGenerator(name=datasets.Split.TRAIN, gen_kwargs={"filepath": downloaded_files["train"]}),
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datasets.SplitGenerator(name=datasets.Split.VALIDATION, gen_kwargs={"filepath": downloaded_files["dev"]}),
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datasets.SplitGenerator(name=datasets.Split.TEST, gen_kwargs={"filepath": downloaded_files["test"]}),
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]
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def _generate_examples(self, filepath):
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logger.info("⏳ Generating examples from = %s", filepath)
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with open(filepath, encoding="utf-8") as f:
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guid = 0
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tokens = []
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ner_tags = []
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for line in f:
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if line == "" or line == "\n":
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if tokens:
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yield guid, {
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"id": str(guid),
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"tokens": tokens,
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"ner_tags": ner_tags,
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}
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guid += 1
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tokens = []
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ner_tags = []
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else:
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# tokens are tab separated
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splits = line.split("\t")
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tokens.append(splits[0])
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if(splits[1].rstrip()=="B-Disease"):
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ner_tags.append("B-DISEASE")
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elif(splits[1].rstrip()=="I-Disease"):
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ner_tags.append("I-DISEASE")
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else:
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ner_tags.append(splits[1].rstrip())
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# last example
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yield guid, {
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"id": str(guid),
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"tokens": tokens,
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"ner_tags": ner_tags,
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}
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