Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP663596.RAAxeCxvoRY9t_lcD6akKb-mnd7C31ZLRsrZdEAENaSoU130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP663596.RAAxeCxvoRY9t_lcD6akKb-mnd7C31ZLRsrZdEAENaSoU130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP663596.RAAxeCxvoRY9t_lcD6akKb-mnd7C31ZLRsrZdEAENaSoU130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP663596.RAAxeCxvoRY9t_lcD6akKb-mnd7C31ZLRsrZdEAENaSoU130_provenance.
- befree-20150227 importedOn "2015-02-27" NP663596.RAAxeCxvoRY9t_lcD6akKb-mnd7C31ZLRsrZdEAENaSoU130_provenance.
- NP663596.RAAxeCxvoRY9t_lcD6akKb-mnd7C31ZLRsrZdEAENaSoU130_assertion wasGeneratedBy ECO_0000203 NP663596.RAAxeCxvoRY9t_lcD6akKb-mnd7C31ZLRsrZdEAENaSoU130_provenance.
- NP663596.RAAxeCxvoRY9t_lcD6akKb-mnd7C31ZLRsrZdEAENaSoU130_assertion wasDerivedFrom befree-20150227 NP663596.RAAxeCxvoRY9t_lcD6akKb-mnd7C31ZLRsrZdEAENaSoU130_provenance.
- NP663596.RAAxeCxvoRY9t_lcD6akKb-mnd7C31ZLRsrZdEAENaSoU130_assertion SIO_000772 17761709 NP663596.RAAxeCxvoRY9t_lcD6akKb-mnd7C31ZLRsrZdEAENaSoU130_provenance.
- NP663596.RAAxeCxvoRY9t_lcD6akKb-mnd7C31ZLRsrZdEAENaSoU130_assertion evidence source_evidence_literature NP663596.RAAxeCxvoRY9t_lcD6akKb-mnd7C31ZLRsrZdEAENaSoU130_provenance.
- NP663596.RAAxeCxvoRY9t_lcD6akKb-mnd7C31ZLRsrZdEAENaSoU130_assertion description "[Carriers of both the RAD51-G135C and CYP3A4-A-290G variants were at highest AML risk (P = 0.003; OR:13,6; 95% CI: 2.0-585.5), suggesting a synergistic effect between these polymorphisms.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP663596.RAAxeCxvoRY9t_lcD6akKb-mnd7C31ZLRsrZdEAENaSoU130_provenance.