Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP939477.RADmtcobHCYDYaTYaIAZbaIEA3luObnSUlkMCiDmf0K7w130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP939477.RADmtcobHCYDYaTYaIAZbaIEA3luObnSUlkMCiDmf0K7w130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP939477.RADmtcobHCYDYaTYaIAZbaIEA3luObnSUlkMCiDmf0K7w130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP939477.RADmtcobHCYDYaTYaIAZbaIEA3luObnSUlkMCiDmf0K7w130_provenance.
- NP939477.RADmtcobHCYDYaTYaIAZbaIEA3luObnSUlkMCiDmf0K7w130_assertion description "[For idiopathic VTE, in addition to the factor V (Leiden) mutation (odds ratio [OR], 5.13; 95% confidence interval [CI], 3.24 to 8.14; P<0.0001; false discovery rate [FDR], P<0.0001), an N291S lipoprotein lipase gene polymorphism (OR, 3.09; 95% CI, 1.56 to 6.09; P=0.001; FDR, P=0.036) and a Q27E beta2-adrenergic receptor gene polymorphism (OR, 1.40; 95% CI, 1.09 to 1.79; P=0.006; FDR, P=0.036) were found to be significantly associated with increased risk.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP939477.RADmtcobHCYDYaTYaIAZbaIEA3luObnSUlkMCiDmf0K7w130_provenance.
- NP939477.RADmtcobHCYDYaTYaIAZbaIEA3luObnSUlkMCiDmf0K7w130_assertion evidence source_evidence_literature NP939477.RADmtcobHCYDYaTYaIAZbaIEA3luObnSUlkMCiDmf0K7w130_provenance.
- NP939477.RADmtcobHCYDYaTYaIAZbaIEA3luObnSUlkMCiDmf0K7w130_assertion SIO_000772 16651467 NP939477.RADmtcobHCYDYaTYaIAZbaIEA3luObnSUlkMCiDmf0K7w130_provenance.
- NP939477.RADmtcobHCYDYaTYaIAZbaIEA3luObnSUlkMCiDmf0K7w130_assertion wasDerivedFrom befree-20140225 NP939477.RADmtcobHCYDYaTYaIAZbaIEA3luObnSUlkMCiDmf0K7w130_provenance.
- NP939477.RADmtcobHCYDYaTYaIAZbaIEA3luObnSUlkMCiDmf0K7w130_assertion wasGeneratedBy ECO_0000203 NP939477.RADmtcobHCYDYaTYaIAZbaIEA3luObnSUlkMCiDmf0K7w130_provenance.
- befree-20140225 importedOn "2014-02-25" NP939477.RADmtcobHCYDYaTYaIAZbaIEA3luObnSUlkMCiDmf0K7w130_provenance.