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- source_evidence_literature type ECO_0000212 NP98125.RAiEO_wMYNucxV7OqA50_pR8r_IVD_gQ5wJvjUn-9TWLQ130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP98125.RAiEO_wMYNucxV7OqA50_pR8r_IVD_gQ5wJvjUn-9TWLQ130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP98125.RAiEO_wMYNucxV7OqA50_pR8r_IVD_gQ5wJvjUn-9TWLQ130_provenance.
- NP98125.RAiEO_wMYNucxV7OqA50_pR8r_IVD_gQ5wJvjUn-9TWLQ130_assertion description "[Variants located within the gene TCF7L2 are strongly associated with T2D but not with MS, providing support to previous evidence indicating that polymorphisms at the TCF7L2 gene increase T2D risk. In contrast, the non-synonymous ADRB3 rs4994 polymorphism ]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP98125.RAiEO_wMYNucxV7OqA50_pR8r_IVD_gQ5wJvjUn-9TWLQ130_provenance.
- NP98125.RAiEO_wMYNucxV7OqA50_pR8r_IVD_gQ5wJvjUn-9TWLQ130_assertion evidence source_evidence_literature NP98125.RAiEO_wMYNucxV7OqA50_pR8r_IVD_gQ5wJvjUn-9TWLQ130_provenance.
- NP98125.RAiEO_wMYNucxV7OqA50_pR8r_IVD_gQ5wJvjUn-9TWLQ130_assertion SIO_000772 20503258 NP98125.RAiEO_wMYNucxV7OqA50_pR8r_IVD_gQ5wJvjUn-9TWLQ130_provenance.
- NP98125.RAiEO_wMYNucxV7OqA50_pR8r_IVD_gQ5wJvjUn-9TWLQ130_assertion wasDerivedFrom gad-20150221 NP98125.RAiEO_wMYNucxV7OqA50_pR8r_IVD_gQ5wJvjUn-9TWLQ130_provenance.
- NP98125.RAiEO_wMYNucxV7OqA50_pR8r_IVD_gQ5wJvjUn-9TWLQ130_assertion wasGeneratedBy ECO_0000203 NP98125.RAiEO_wMYNucxV7OqA50_pR8r_IVD_gQ5wJvjUn-9TWLQ130_provenance.
- gad-20150221 importedOn "2015-02-21" NP98125.RAiEO_wMYNucxV7OqA50_pR8r_IVD_gQ5wJvjUn-9TWLQ130_provenance.