--- dataset_info: features: - name: text dtype: string - name: relation dtype: string - name: h struct: - name: id dtype: int64 - name: name dtype: string - name: pos sequence: int64 - name: t struct: - name: id dtype: string - name: name dtype: string - name: pos sequence: int64 splits: - name: train num_bytes: 54491244 num_examples: 178264 - name: validation num_bytes: 6118764 num_examples: 20193 - name: test num_bytes: 6168865 num_examples: 20516 download_size: 35878376 dataset_size: 66778873 configs: - config_name: default data_files: - split: train path: data/train-* - split: validation path: data/validation-* - split: test path: data/test-* task_categories: - text-classification language: - en tags: - biology - relation-classification - medical - relation-extraction - gene - disease - gda pretty_name: TBGA size_categories: - 100K TBGA is a comprehensive dataset created for the purpose of Gene-Disease Association (GDA) extraction, generated from over 700,000 publications. It features more than 200,000 instances and 100,000 unique gene-disease pairs. Each instance in the dataset includes the specific sentence from which the GDA was extracted, the extracted GDA itself, and detailed information about the gene-disease pair involved. This dataset was semi-automatically annotated by Marchesin and Silvello using data sourced from the DisGeNET database, which houses one of the most extensive collections of genes and variants associated with human diseases. The dataset follows the OpenNRE format and contains the following relations: ```json {"NA": 0, "therapeutic": 1, "biomarker": 2, "genomic_alterations": 3} ``` ### Languages The language in the dataset is English. ## Dataset Structure ### Dataset Instances An example of 'train' looks as follows: ```json { "text": "A monocyte chemoattractant protein-1 gene polymorphism is associated with occult ischemia in a high-risk asymptomatic population.", "relation": "NA", "h": { "id": 6347, "name": "CCL2", "pos": [2, 34] }, "t": { "id": "C0231221", "name": "Asymptomatic", "pos": [105, 12] } } ``` ### Data Fields - `text`: the text of this example, a `string` feature. - `h`: the gene entity - `id`: NCBI Entrez ID associated with the gene entity, a `string` feature. - `pos`: list consisting of starting position and length of the gene mention withintext, a list of `int32` features. - `name`: NCBI official gene symbol associated with the gene entity (not the text of the mention), a `string` feature. - `t`: the disease entity - `id`: UMLS Concept Unique Identifier (CUI) associated with the disease entity, a `string` feature. - `pos`: list consisting of starting position and length of the disease mention withintext, a list of `int32` features. - `name`: UMLS preferred term associated with the disease entity (not the text of the mention), a `string` feature. - `relation`: a class label associated with the given GDA. ## Citation **BibTeX:** ``` @article{marchesin-silvello-2022, title = "TBGA: a large-scale Gene-Disease Association dataset for Biomedical Relation Extraction", author = "S. Marchesin and G. Silvello", journal = "BMC Bioinformatics", year = "2022", url = "https://bmcbioinformatics.biomedcentral.com/articles/10.1186/s12859-022-04646-6", doi = "10.1186/s12859-022-04646-6", volume = "23", number = "1", pages = "111" } ``` **APA:** - Marchesin, S., & Silvello, G. (2022). TBGA: A large-scale Gene-Disease Association dataset for Biomedical Relation Extraction. BMC Bioinformatics, 23(1), 111. https://doi.org/10.1186/s12859-022-04646-6 ## Dataset Card Authors [@phucdev](https://github.com/phucdev)