| Name |
|---|
Tabula Sapiens Gene-Cell Associations DatasetFrom Tabula Sapiens Gene expression data from Tabula Sapiens scRNA-seq counts |
Pathway Commons Protein-Protein Interactions DatasetFrom Pathway Commons Protein-protein interactions from low-throughput or high-throughput studies aggregated by Pathway Commons from the following databases: Reactome, NCI Pathways, PhosphoSite, HumanCyc, HPRD, PANTHER, DIP, BioGRID, IntAct, BIND, Transfac, MiRTarBase, Drugbank, Recon X, Comparative Toxicogenomics Database, and KEGG |
PFOCR Pathway Figure Associations 2023 Dataset (Archived)From Pathway Figure Optical Character Recognition Sets of genes/proteins extracted from pathway figures in research publications using optical character recognition |
PFOCR Pathway Figure Associations 2024 DatasetFrom Pathway Figure Optical Character Recognition Sets of genes/proteins extracted from pathway figures in research publications using optical character recognition, updated for 2024 |
CTD Gene-Disease Associations DatasetFrom Comparative Toxicogenomics Database Disease-gene interactions from manually curated literature |
DISEASES Curated Gene-Disease Association Evidence Scores Dataset (Archived)From DISEASES Disease gene evidence scores by manual literature curation |
DISEASES Experimental Gene-Disease Association Evidence Scores Dataset (Archived)From DISEASES Disease gene evidence scores by integrating experimental data (GWAS) |
DISEASES Text-mining Gene-Disease Association Evidence Scores Dataset (Archived)From DISEASES Gene-disease co-occurrence scores from text-mining biomedical abstracts |
GAD Gene-Disease Associations DatasetFrom Genetic Association Database Gene-disease associations curated from genetic association studies |
GAD High Level Gene-Disease Associations DatasetFrom Genetic Association Database Gene-disease associations curated from genetic association studies |
GWASdb SNP-Disease Associations DatasetFrom GWASdb SNP-disease association p-values curated from published GWAS |
HPO Gene-Disease Associations DatasetPhenotype-causing gene mutations of human phenotypes from disease knowledgebases |
OMIM Gene-Disease Associations DatasetFrom Online Mendelian Inheritance in Man Disease- or phenotype-causing gene mutations for heritable human diseases or phenotypes curated from biomedical publications |
PhosphoSitePlus Phosphosite-Disease Associations DatasetFrom PhosphoSitePlus Disease-phosphosite associations curated from literature |
DisGeNET Gene-Disease Associations DatasetFrom DisGeNET Gene-disease associations sourced from curated repositories, GWAS catalogues, animal models and the scientific literature |
DISEASES Curated Gene-Disease Association Evidence Scores 2025 DatasetFrom DISEASES Disease gene evidence scores by manual literature curation |
DISEASES Experimental Gene-Disease Association Evidence Scores 2025 DatasetFrom DISEASES Disease gene evidence scores by integrating experimental data (GWAS) |
DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 DatasetFrom DISEASES Gene-disease co-occurrence scores from text-mining biomedical abstracts |
PID Pathways DatasetFrom Pathway Interaction Database Sets of proteins participating in pathways from PID |