Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP327538.RAs8cKkpHU7cOEvR2L-3SRcIMHhRFCrWgPMuuACcniOLA130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP327538.RAs8cKkpHU7cOEvR2L-3SRcIMHhRFCrWgPMuuACcniOLA130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP327538.RAs8cKkpHU7cOEvR2L-3SRcIMHhRFCrWgPMuuACcniOLA130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP327538.RAs8cKkpHU7cOEvR2L-3SRcIMHhRFCrWgPMuuACcniOLA130_provenance.
- NP327538.RAs8cKkpHU7cOEvR2L-3SRcIMHhRFCrWgPMuuACcniOLA130_assertion description "[The frequency of valine (Val)/valine (Val) genotypes for CYP1A1 was 11.3% in cases compared with 5.5% in controls, this polymorphism thus being associated with a significantly increased risk of PCa (odds ratio=2.4, 95% confidence interval (CI)=1.01-5.57).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP327538.RAs8cKkpHU7cOEvR2L-3SRcIMHhRFCrWgPMuuACcniOLA130_provenance.
- NP327538.RAs8cKkpHU7cOEvR2L-3SRcIMHhRFCrWgPMuuACcniOLA130_assertion evidence source_evidence_literature NP327538.RAs8cKkpHU7cOEvR2L-3SRcIMHhRFCrWgPMuuACcniOLA130_provenance.
- NP327538.RAs8cKkpHU7cOEvR2L-3SRcIMHhRFCrWgPMuuACcniOLA130_assertion SIO_000772 11275366 NP327538.RAs8cKkpHU7cOEvR2L-3SRcIMHhRFCrWgPMuuACcniOLA130_provenance.
- NP327538.RAs8cKkpHU7cOEvR2L-3SRcIMHhRFCrWgPMuuACcniOLA130_assertion wasDerivedFrom befree-20140225 NP327538.RAs8cKkpHU7cOEvR2L-3SRcIMHhRFCrWgPMuuACcniOLA130_provenance.
- NP327538.RAs8cKkpHU7cOEvR2L-3SRcIMHhRFCrWgPMuuACcniOLA130_assertion wasGeneratedBy ECO_0000203 NP327538.RAs8cKkpHU7cOEvR2L-3SRcIMHhRFCrWgPMuuACcniOLA130_provenance.
- befree-20140225 importedOn "2014-02-25" NP327538.RAs8cKkpHU7cOEvR2L-3SRcIMHhRFCrWgPMuuACcniOLA130_provenance.