Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP872226.RAQ9Rva8YD3_wMyFiG-q3j7H17MEYAVjtgCFfMvMTOGqI130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP872226.RAQ9Rva8YD3_wMyFiG-q3j7H17MEYAVjtgCFfMvMTOGqI130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP872226.RAQ9Rva8YD3_wMyFiG-q3j7H17MEYAVjtgCFfMvMTOGqI130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP872226.RAQ9Rva8YD3_wMyFiG-q3j7H17MEYAVjtgCFfMvMTOGqI130_provenance.
- NP872226.RAQ9Rva8YD3_wMyFiG-q3j7H17MEYAVjtgCFfMvMTOGqI130_assertion description "[Nominally significant associations were also observed between T2D and the SIRT1 rs3758391 SNP and MS and the HHEX rs5015480 polymorphism.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP872226.RAQ9Rva8YD3_wMyFiG-q3j7H17MEYAVjtgCFfMvMTOGqI130_provenance.
- NP872226.RAQ9Rva8YD3_wMyFiG-q3j7H17MEYAVjtgCFfMvMTOGqI130_assertion evidence source_evidence_literature NP872226.RAQ9Rva8YD3_wMyFiG-q3j7H17MEYAVjtgCFfMvMTOGqI130_provenance.
- NP872226.RAQ9Rva8YD3_wMyFiG-q3j7H17MEYAVjtgCFfMvMTOGqI130_assertion SIO_000772 20503258 NP872226.RAQ9Rva8YD3_wMyFiG-q3j7H17MEYAVjtgCFfMvMTOGqI130_provenance.
- NP872226.RAQ9Rva8YD3_wMyFiG-q3j7H17MEYAVjtgCFfMvMTOGqI130_assertion wasDerivedFrom befree-20150227 NP872226.RAQ9Rva8YD3_wMyFiG-q3j7H17MEYAVjtgCFfMvMTOGqI130_provenance.
- NP872226.RAQ9Rva8YD3_wMyFiG-q3j7H17MEYAVjtgCFfMvMTOGqI130_assertion wasGeneratedBy ECO_0000203 NP872226.RAQ9Rva8YD3_wMyFiG-q3j7H17MEYAVjtgCFfMvMTOGqI130_provenance.
- befree-20150227 importedOn "2015-02-27" NP872226.RAQ9Rva8YD3_wMyFiG-q3j7H17MEYAVjtgCFfMvMTOGqI130_provenance.