Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP101828.RA0cm0Pa4qh8l69P__DCLdF2WD_oE09810Vgxf-cr4WT0130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP101828.RA0cm0Pa4qh8l69P__DCLdF2WD_oE09810Vgxf-cr4WT0130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP101828.RA0cm0Pa4qh8l69P__DCLdF2WD_oE09810Vgxf-cr4WT0130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP101828.RA0cm0Pa4qh8l69P__DCLdF2WD_oE09810Vgxf-cr4WT0130_provenance.
- NP101828.RA0cm0Pa4qh8l69P__DCLdF2WD_oE09810Vgxf-cr4WT0130_assertion description "[We examined the association of variants in genes encoding several transcription factors (TCF1, TCF2, HNF4A, ISL1, IPF1, NEUROG3, PAX6, NKX2-2, NKX6-1, and NEUROD1) and genes encoding the ATP-sensitive K(+) channel subunits Kir6.2 (KCNJ11) and SUR1 (ABCC8) with type 2 diabetes in a Japanese cohort of 2,834 subjects.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP101828.RA0cm0Pa4qh8l69P__DCLdF2WD_oE09810Vgxf-cr4WT0130_provenance.
- NP101828.RA0cm0Pa4qh8l69P__DCLdF2WD_oE09810Vgxf-cr4WT0130_assertion evidence source_evidence_literature NP101828.RA0cm0Pa4qh8l69P__DCLdF2WD_oE09810Vgxf-cr4WT0130_provenance.
- NP101828.RA0cm0Pa4qh8l69P__DCLdF2WD_oE09810Vgxf-cr4WT0130_assertion SIO_000772 16873704 NP101828.RA0cm0Pa4qh8l69P__DCLdF2WD_oE09810Vgxf-cr4WT0130_provenance.
- NP101828.RA0cm0Pa4qh8l69P__DCLdF2WD_oE09810Vgxf-cr4WT0130_assertion wasDerivedFrom gad-20150221 NP101828.RA0cm0Pa4qh8l69P__DCLdF2WD_oE09810Vgxf-cr4WT0130_provenance.
- NP101828.RA0cm0Pa4qh8l69P__DCLdF2WD_oE09810Vgxf-cr4WT0130_assertion wasGeneratedBy ECO_0000203 NP101828.RA0cm0Pa4qh8l69P__DCLdF2WD_oE09810Vgxf-cr4WT0130_provenance.
- gad-20150221 importedOn "2015-02-21" NP101828.RA0cm0Pa4qh8l69P__DCLdF2WD_oE09810Vgxf-cr4WT0130_provenance.