Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP882222.RAVC4BpYH1al5hrJAPfHw0Yx3iH8nHXhcMdexRfg8QG8o130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP882222.RAVC4BpYH1al5hrJAPfHw0Yx3iH8nHXhcMdexRfg8QG8o130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP882222.RAVC4BpYH1al5hrJAPfHw0Yx3iH8nHXhcMdexRfg8QG8o130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP882222.RAVC4BpYH1al5hrJAPfHw0Yx3iH8nHXhcMdexRfg8QG8o130_provenance.
- NP882222.RAVC4BpYH1al5hrJAPfHw0Yx3iH8nHXhcMdexRfg8QG8o130_assertion wasGeneratedBy ECO_0000203 NP882222.RAVC4BpYH1al5hrJAPfHw0Yx3iH8nHXhcMdexRfg8QG8o130_provenance.
- NP882222.RAVC4BpYH1al5hrJAPfHw0Yx3iH8nHXhcMdexRfg8QG8o130_assertion wasDerivedFrom befree-20140225 NP882222.RAVC4BpYH1al5hrJAPfHw0Yx3iH8nHXhcMdexRfg8QG8o130_provenance.
- NP882222.RAVC4BpYH1al5hrJAPfHw0Yx3iH8nHXhcMdexRfg8QG8o130_assertion SIO_000772 17761709 NP882222.RAVC4BpYH1al5hrJAPfHw0Yx3iH8nHXhcMdexRfg8QG8o130_provenance.
- NP882222.RAVC4BpYH1al5hrJAPfHw0Yx3iH8nHXhcMdexRfg8QG8o130_assertion evidence source_evidence_literature NP882222.RAVC4BpYH1al5hrJAPfHw0Yx3iH8nHXhcMdexRfg8QG8o130_provenance.
- NP882222.RAVC4BpYH1al5hrJAPfHw0Yx3iH8nHXhcMdexRfg8QG8o130_assertion description "[We found a significantly higher prevalence of the polymorphic variants RAD51-G135C and CYP3A4-A-290G genes in AML cases, when compared with controls (P = 0.02 and P = 0.04), increasing the risk of AML 2.1-folds (95% CI: 1.1-4.0) and 3.2-fold (95% CI: 1.1-11.5), respectively.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP882222.RAVC4BpYH1al5hrJAPfHw0Yx3iH8nHXhcMdexRfg8QG8o130_provenance.
- befree-20140225 importedOn "2014-02-25" NP882222.RAVC4BpYH1al5hrJAPfHw0Yx3iH8nHXhcMdexRfg8QG8o130_provenance.