Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP802129.RAoJGfidEB7p3_02MIivaiMaS40iqCMrJuiOgRlE4lQaA130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP802129.RAoJGfidEB7p3_02MIivaiMaS40iqCMrJuiOgRlE4lQaA130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP802129.RAoJGfidEB7p3_02MIivaiMaS40iqCMrJuiOgRlE4lQaA130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP802129.RAoJGfidEB7p3_02MIivaiMaS40iqCMrJuiOgRlE4lQaA130_provenance.
- NP802129.RAoJGfidEB7p3_02MIivaiMaS40iqCMrJuiOgRlE4lQaA130_assertion description "[We genotyped 146 Caucasian Lynch syndrome mutation carriers for a 5'-untranslated region polymorphism in cytochrome P450 17A1 (CYP17; c.-34T-->C) and an exon 4 polymorphism in catechol O-methyltransferase (COMT; c.472G-->A); 50 mutation carriers had developed colon or rectal cancer at last contact.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP802129.RAoJGfidEB7p3_02MIivaiMaS40iqCMrJuiOgRlE4lQaA130_provenance.
- NP802129.RAoJGfidEB7p3_02MIivaiMaS40iqCMrJuiOgRlE4lQaA130_assertion evidence source_evidence_literature NP802129.RAoJGfidEB7p3_02MIivaiMaS40iqCMrJuiOgRlE4lQaA130_provenance.
- NP802129.RAoJGfidEB7p3_02MIivaiMaS40iqCMrJuiOgRlE4lQaA130_assertion SIO_000772 17606708 NP802129.RAoJGfidEB7p3_02MIivaiMaS40iqCMrJuiOgRlE4lQaA130_provenance.
- NP802129.RAoJGfidEB7p3_02MIivaiMaS40iqCMrJuiOgRlE4lQaA130_assertion wasDerivedFrom befree-20140225 NP802129.RAoJGfidEB7p3_02MIivaiMaS40iqCMrJuiOgRlE4lQaA130_provenance.
- NP802129.RAoJGfidEB7p3_02MIivaiMaS40iqCMrJuiOgRlE4lQaA130_assertion wasGeneratedBy ECO_0000203 NP802129.RAoJGfidEB7p3_02MIivaiMaS40iqCMrJuiOgRlE4lQaA130_provenance.
- befree-20140225 importedOn "2014-02-25" NP802129.RAoJGfidEB7p3_02MIivaiMaS40iqCMrJuiOgRlE4lQaA130_provenance.