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- source_evidence_literature type ECO_0000212 NP122758.RA85qHy2Jw_MU8ThiV71LYquyaCBj1cLD7sx0Jm2vUy5c130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP122758.RA85qHy2Jw_MU8ThiV71LYquyaCBj1cLD7sx0Jm2vUy5c130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP122758.RA85qHy2Jw_MU8ThiV71LYquyaCBj1cLD7sx0Jm2vUy5c130_provenance.
- NP122758.RA85qHy2Jw_MU8ThiV71LYquyaCBj1cLD7sx0Jm2vUy5c130_assertion description "[In addition to TCF7L2, SLC30A8 and HHEX, initially identified by the French GWA scan, CDKAL1, IGFBP2 and CDKN2A/2B strongly associate with T2D in French individuals, and mostly in populations of Central European descent but not in Moroccan subjects.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP122758.RA85qHy2Jw_MU8ThiV71LYquyaCBj1cLD7sx0Jm2vUy5c130_provenance.
- NP122758.RA85qHy2Jw_MU8ThiV71LYquyaCBj1cLD7sx0Jm2vUy5c130_assertion evidence source_evidence_literature NP122758.RA85qHy2Jw_MU8ThiV71LYquyaCBj1cLD7sx0Jm2vUy5c130_provenance.
- NP122758.RA85qHy2Jw_MU8ThiV71LYquyaCBj1cLD7sx0Jm2vUy5c130_assertion SIO_000772 18461161 NP122758.RA85qHy2Jw_MU8ThiV71LYquyaCBj1cLD7sx0Jm2vUy5c130_provenance.
- NP122758.RA85qHy2Jw_MU8ThiV71LYquyaCBj1cLD7sx0Jm2vUy5c130_assertion wasDerivedFrom gad-20150221 NP122758.RA85qHy2Jw_MU8ThiV71LYquyaCBj1cLD7sx0Jm2vUy5c130_provenance.
- NP122758.RA85qHy2Jw_MU8ThiV71LYquyaCBj1cLD7sx0Jm2vUy5c130_assertion wasGeneratedBy ECO_0000203 NP122758.RA85qHy2Jw_MU8ThiV71LYquyaCBj1cLD7sx0Jm2vUy5c130_provenance.
- gad-20150221 importedOn "2015-02-21" NP122758.RA85qHy2Jw_MU8ThiV71LYquyaCBj1cLD7sx0Jm2vUy5c130_provenance.