Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP336913.RANho0w59z04Gd1gbLufSqIgsiH1we_exXsOLt578xpsg130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP336913.RANho0w59z04Gd1gbLufSqIgsiH1we_exXsOLt578xpsg130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP336913.RANho0w59z04Gd1gbLufSqIgsiH1we_exXsOLt578xpsg130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP336913.RANho0w59z04Gd1gbLufSqIgsiH1we_exXsOLt578xpsg130_provenance.
- NP336913.RANho0w59z04Gd1gbLufSqIgsiH1we_exXsOLt578xpsg130_assertion description "[We identified a variant in a single PPAR pathway gene, TLL1, that is associated with the extent of CAD independently of clinical predictors, specifically in patients with type 2 diabetes mellitus and CAD.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP336913.RANho0w59z04Gd1gbLufSqIgsiH1we_exXsOLt578xpsg130_provenance.
- NP336913.RANho0w59z04Gd1gbLufSqIgsiH1we_exXsOLt578xpsg130_assertion evidence source_evidence_literature NP336913.RANho0w59z04Gd1gbLufSqIgsiH1we_exXsOLt578xpsg130_provenance.
- NP336913.RANho0w59z04Gd1gbLufSqIgsiH1we_exXsOLt578xpsg130_assertion SIO_000772 21911782 NP336913.RANho0w59z04Gd1gbLufSqIgsiH1we_exXsOLt578xpsg130_provenance.
- NP336913.RANho0w59z04Gd1gbLufSqIgsiH1we_exXsOLt578xpsg130_assertion wasDerivedFrom befree-20140225 NP336913.RANho0w59z04Gd1gbLufSqIgsiH1we_exXsOLt578xpsg130_provenance.
- NP336913.RANho0w59z04Gd1gbLufSqIgsiH1we_exXsOLt578xpsg130_assertion wasGeneratedBy ECO_0000203 NP336913.RANho0w59z04Gd1gbLufSqIgsiH1we_exXsOLt578xpsg130_provenance.
- befree-20140225 importedOn "2014-02-25" NP336913.RANho0w59z04Gd1gbLufSqIgsiH1we_exXsOLt578xpsg130_provenance.