Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP45099.RAaf1-tfaK4DNfFxsfbhgkpGDFjAY_ny3dQMMnmVoyU5U130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP45099.RAaf1-tfaK4DNfFxsfbhgkpGDFjAY_ny3dQMMnmVoyU5U130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP45099.RAaf1-tfaK4DNfFxsfbhgkpGDFjAY_ny3dQMMnmVoyU5U130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP45099.RAaf1-tfaK4DNfFxsfbhgkpGDFjAY_ny3dQMMnmVoyU5U130_provenance.
- NP45099.RAaf1-tfaK4DNfFxsfbhgkpGDFjAY_ny3dQMMnmVoyU5U130_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 is associated with T2D and MS.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP45099.RAaf1-tfaK4DNfFxsfbhgkpGDFjAY_ny3dQMMnmVoyU5U130_provenance.
- NP45099.RAaf1-tfaK4DNfFxsfbhgkpGDFjAY_ny3dQMMnmVoyU5U130_assertion evidence source_evidence_literature NP45099.RAaf1-tfaK4DNfFxsfbhgkpGDFjAY_ny3dQMMnmVoyU5U130_provenance.
- NP45099.RAaf1-tfaK4DNfFxsfbhgkpGDFjAY_ny3dQMMnmVoyU5U130_assertion SIO_000772 20503258 NP45099.RAaf1-tfaK4DNfFxsfbhgkpGDFjAY_ny3dQMMnmVoyU5U130_provenance.
- NP45099.RAaf1-tfaK4DNfFxsfbhgkpGDFjAY_ny3dQMMnmVoyU5U130_assertion wasDerivedFrom gad-20130706 NP45099.RAaf1-tfaK4DNfFxsfbhgkpGDFjAY_ny3dQMMnmVoyU5U130_provenance.
- NP45099.RAaf1-tfaK4DNfFxsfbhgkpGDFjAY_ny3dQMMnmVoyU5U130_assertion wasGeneratedBy ECO_0000203 NP45099.RAaf1-tfaK4DNfFxsfbhgkpGDFjAY_ny3dQMMnmVoyU5U130_provenance.
- gad-20130706 importedOn "2013-07-06" NP45099.RAaf1-tfaK4DNfFxsfbhgkpGDFjAY_ny3dQMMnmVoyU5U130_provenance.