Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP563193.RAWJDwmqQiG7blKQKjq7RvWNsvawR4ZKnEO37PoRCJC5M130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP563193.RAWJDwmqQiG7blKQKjq7RvWNsvawR4ZKnEO37PoRCJC5M130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP563193.RAWJDwmqQiG7blKQKjq7RvWNsvawR4ZKnEO37PoRCJC5M130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP563193.RAWJDwmqQiG7blKQKjq7RvWNsvawR4ZKnEO37PoRCJC5M130_provenance.
- NP563193.RAWJDwmqQiG7blKQKjq7RvWNsvawR4ZKnEO37PoRCJC5M130_assertion description "[The presence of I allele was associated with an increased risk of CD (OR 1.35) and the effect of I allele was consistent with a recessive genetic model (P<0.001).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP563193.RAWJDwmqQiG7blKQKjq7RvWNsvawR4ZKnEO37PoRCJC5M130_provenance.
- NP563193.RAWJDwmqQiG7blKQKjq7RvWNsvawR4ZKnEO37PoRCJC5M130_assertion evidence source_evidence_literature NP563193.RAWJDwmqQiG7blKQKjq7RvWNsvawR4ZKnEO37PoRCJC5M130_provenance.
- NP563193.RAWJDwmqQiG7blKQKjq7RvWNsvawR4ZKnEO37PoRCJC5M130_assertion SIO_000772 20823837 NP563193.RAWJDwmqQiG7blKQKjq7RvWNsvawR4ZKnEO37PoRCJC5M130_provenance.
- NP563193.RAWJDwmqQiG7blKQKjq7RvWNsvawR4ZKnEO37PoRCJC5M130_assertion wasDerivedFrom befree-20140225 NP563193.RAWJDwmqQiG7blKQKjq7RvWNsvawR4ZKnEO37PoRCJC5M130_provenance.
- NP563193.RAWJDwmqQiG7blKQKjq7RvWNsvawR4ZKnEO37PoRCJC5M130_assertion wasGeneratedBy ECO_0000203 NP563193.RAWJDwmqQiG7blKQKjq7RvWNsvawR4ZKnEO37PoRCJC5M130_provenance.
- befree-20140225 importedOn "2014-02-25" NP563193.RAWJDwmqQiG7blKQKjq7RvWNsvawR4ZKnEO37PoRCJC5M130_provenance.