Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP1247777.RAov8dv2dN212JGGrF30ZHFd9D7y7gdubWyTy0sHFPWdw130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP1247777.RAov8dv2dN212JGGrF30ZHFd9D7y7gdubWyTy0sHFPWdw130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP1247777.RAov8dv2dN212JGGrF30ZHFd9D7y7gdubWyTy0sHFPWdw130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP1247777.RAov8dv2dN212JGGrF30ZHFd9D7y7gdubWyTy0sHFPWdw130_provenance.
- NP1247777.RAov8dv2dN212JGGrF30ZHFd9D7y7gdubWyTy0sHFPWdw130_assertion description "[MG 18?2 showed an enrichment (P-value?=?0.002) of significant associations with CHD-associated SNPs (P-value?=?1.2�10-7 for association with rs964184 in the ZNF259/APOA5 region) and a weak, but positive causal effect (odds ratio?=?1.05 per SD increment in MG 18?2, P-value?=?0.05) on CHD, as suggested by Mendelian randomization analysis.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1247777.RAov8dv2dN212JGGrF30ZHFd9D7y7gdubWyTy0sHFPWdw130_provenance.
- NP1247777.RAov8dv2dN212JGGrF30ZHFd9D7y7gdubWyTy0sHFPWdw130_assertion evidence source_evidence_literature NP1247777.RAov8dv2dN212JGGrF30ZHFd9D7y7gdubWyTy0sHFPWdw130_provenance.
- NP1247777.RAov8dv2dN212JGGrF30ZHFd9D7y7gdubWyTy0sHFPWdw130_assertion SIO_000772 25502724 NP1247777.RAov8dv2dN212JGGrF30ZHFd9D7y7gdubWyTy0sHFPWdw130_provenance.
- NP1247777.RAov8dv2dN212JGGrF30ZHFd9D7y7gdubWyTy0sHFPWdw130_assertion wasDerivedFrom befree-2016 NP1247777.RAov8dv2dN212JGGrF30ZHFd9D7y7gdubWyTy0sHFPWdw130_provenance.
- NP1247777.RAov8dv2dN212JGGrF30ZHFd9D7y7gdubWyTy0sHFPWdw130_assertion wasGeneratedBy ECO_0000203 NP1247777.RAov8dv2dN212JGGrF30ZHFd9D7y7gdubWyTy0sHFPWdw130_provenance.
- befree-2016 importedOn "2016-02-19" NP1247777.RAov8dv2dN212JGGrF30ZHFd9D7y7gdubWyTy0sHFPWdw130_provenance.