Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP367315.RArO-X-NFJvABUIh2d0Qi7WKBOji3C9g9Gl_VPXJ-tKCY130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP367315.RArO-X-NFJvABUIh2d0Qi7WKBOji3C9g9Gl_VPXJ-tKCY130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP367315.RArO-X-NFJvABUIh2d0Qi7WKBOji3C9g9Gl_VPXJ-tKCY130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP367315.RArO-X-NFJvABUIh2d0Qi7WKBOji3C9g9Gl_VPXJ-tKCY130_provenance.
- NP367315.RArO-X-NFJvABUIh2d0Qi7WKBOji3C9g9Gl_VPXJ-tKCY130_assertion description "[Gene-gene interaction testing suggested several cancer-NAT2 associations, with association strongest among persons without a CYP1A1 variant (*2C or *4) allele (OR 1.77, 95% CI 1.20-2.60, p value = .03) or with a variant MPO (463A) allele (OR 2.38, 95% CI 1.34-4.21, p value = .05).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP367315.RArO-X-NFJvABUIh2d0Qi7WKBOji3C9g9Gl_VPXJ-tKCY130_provenance.
- NP367315.RArO-X-NFJvABUIh2d0Qi7WKBOji3C9g9Gl_VPXJ-tKCY130_assertion evidence source_evidence_literature NP367315.RArO-X-NFJvABUIh2d0Qi7WKBOji3C9g9Gl_VPXJ-tKCY130_provenance.
- NP367315.RArO-X-NFJvABUIh2d0Qi7WKBOji3C9g9Gl_VPXJ-tKCY130_assertion SIO_000772 18642288 NP367315.RArO-X-NFJvABUIh2d0Qi7WKBOji3C9g9Gl_VPXJ-tKCY130_provenance.
- NP367315.RArO-X-NFJvABUIh2d0Qi7WKBOji3C9g9Gl_VPXJ-tKCY130_assertion wasDerivedFrom befree-20140225 NP367315.RArO-X-NFJvABUIh2d0Qi7WKBOji3C9g9Gl_VPXJ-tKCY130_provenance.
- NP367315.RArO-X-NFJvABUIh2d0Qi7WKBOji3C9g9Gl_VPXJ-tKCY130_assertion wasGeneratedBy ECO_0000203 NP367315.RArO-X-NFJvABUIh2d0Qi7WKBOji3C9g9Gl_VPXJ-tKCY130_provenance.
- befree-20140225 importedOn "2014-02-25" NP367315.RArO-X-NFJvABUIh2d0Qi7WKBOji3C9g9Gl_VPXJ-tKCY130_provenance.