Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP821764.RA-NlEtUp-wU5jNLY-HQTYzp6BgVdDr1tVzmYrzlPcx0Y130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP821764.RA-NlEtUp-wU5jNLY-HQTYzp6BgVdDr1tVzmYrzlPcx0Y130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP821764.RA-NlEtUp-wU5jNLY-HQTYzp6BgVdDr1tVzmYrzlPcx0Y130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP821764.RA-NlEtUp-wU5jNLY-HQTYzp6BgVdDr1tVzmYrzlPcx0Y130_provenance.
- NP821764.RA-NlEtUp-wU5jNLY-HQTYzp6BgVdDr1tVzmYrzlPcx0Y130_assertion description "[The carriage rates of the alleles I and -634C were significantly more frequent in patients with BD than in healthy controls [p corr = 0.036, OR 1.8 (95% CI 1.1-2.9) and p corr = 0.05, OR 1.8 (95% CI 1.1-3.0), respectively].]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP821764.RA-NlEtUp-wU5jNLY-HQTYzp6BgVdDr1tVzmYrzlPcx0Y130_provenance.
- NP821764.RA-NlEtUp-wU5jNLY-HQTYzp6BgVdDr1tVzmYrzlPcx0Y130_assertion evidence source_evidence_literature NP821764.RA-NlEtUp-wU5jNLY-HQTYzp6BgVdDr1tVzmYrzlPcx0Y130_provenance.
- NP821764.RA-NlEtUp-wU5jNLY-HQTYzp6BgVdDr1tVzmYrzlPcx0Y130_assertion SIO_000772 15338501 NP821764.RA-NlEtUp-wU5jNLY-HQTYzp6BgVdDr1tVzmYrzlPcx0Y130_provenance.
- NP821764.RA-NlEtUp-wU5jNLY-HQTYzp6BgVdDr1tVzmYrzlPcx0Y130_assertion wasDerivedFrom befree-20140225 NP821764.RA-NlEtUp-wU5jNLY-HQTYzp6BgVdDr1tVzmYrzlPcx0Y130_provenance.
- NP821764.RA-NlEtUp-wU5jNLY-HQTYzp6BgVdDr1tVzmYrzlPcx0Y130_assertion wasGeneratedBy ECO_0000203 NP821764.RA-NlEtUp-wU5jNLY-HQTYzp6BgVdDr1tVzmYrzlPcx0Y130_provenance.
- befree-20140225 importedOn "2014-02-25" NP821764.RA-NlEtUp-wU5jNLY-HQTYzp6BgVdDr1tVzmYrzlPcx0Y130_provenance.