Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP815143.RAY-nG9UL75tMJRw7zzJolDfK78HK-BvYMWGd0Uj2PjoE130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP815143.RAY-nG9UL75tMJRw7zzJolDfK78HK-BvYMWGd0Uj2PjoE130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP815143.RAY-nG9UL75tMJRw7zzJolDfK78HK-BvYMWGd0Uj2PjoE130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP815143.RAY-nG9UL75tMJRw7zzJolDfK78HK-BvYMWGd0Uj2PjoE130_provenance.
- NP815143.RAY-nG9UL75tMJRw7zzJolDfK78HK-BvYMWGd0Uj2PjoE130_assertion description "[We identified genetic associations between Beh�et's disease and single-nucleotide polymorphisms (SNPs) in KIAA1529, CPVL, LOC100129342, UBASH3B, and UBAC2 (odds ratio = 2.04, 2.26, 1.84, 1.71, and 1.61, respectively; P value = 4.2 x 10-5, 1.0 x 10-4, 3.0 x 10-4, 1.5 x 10-3, and 5.8 x 10-3, respectively).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP815143.RAY-nG9UL75tMJRw7zzJolDfK78HK-BvYMWGd0Uj2PjoE130_provenance.
- NP815143.RAY-nG9UL75tMJRw7zzJolDfK78HK-BvYMWGd0Uj2PjoE130_assertion evidence source_evidence_literature NP815143.RAY-nG9UL75tMJRw7zzJolDfK78HK-BvYMWGd0Uj2PjoE130_provenance.
- NP815143.RAY-nG9UL75tMJRw7zzJolDfK78HK-BvYMWGd0Uj2PjoE130_assertion SIO_000772 19442274 NP815143.RAY-nG9UL75tMJRw7zzJolDfK78HK-BvYMWGd0Uj2PjoE130_provenance.
- NP815143.RAY-nG9UL75tMJRw7zzJolDfK78HK-BvYMWGd0Uj2PjoE130_assertion wasDerivedFrom befree-20140225 NP815143.RAY-nG9UL75tMJRw7zzJolDfK78HK-BvYMWGd0Uj2PjoE130_provenance.
- NP815143.RAY-nG9UL75tMJRw7zzJolDfK78HK-BvYMWGd0Uj2PjoE130_assertion wasGeneratedBy ECO_0000203 NP815143.RAY-nG9UL75tMJRw7zzJolDfK78HK-BvYMWGd0Uj2PjoE130_provenance.
- befree-20140225 importedOn "2014-02-25" NP815143.RAY-nG9UL75tMJRw7zzJolDfK78HK-BvYMWGd0Uj2PjoE130_provenance.