Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP158096.RAkFGDYQCxecHzjPXkYlcVWgVS98J7vaI1jxz5mvlwHuc130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP158096.RAkFGDYQCxecHzjPXkYlcVWgVS98J7vaI1jxz5mvlwHuc130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP158096.RAkFGDYQCxecHzjPXkYlcVWgVS98J7vaI1jxz5mvlwHuc130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP158096.RAkFGDYQCxecHzjPXkYlcVWgVS98J7vaI1jxz5mvlwHuc130_provenance.
- NP158096.RAkFGDYQCxecHzjPXkYlcVWgVS98J7vaI1jxz5mvlwHuc130_assertion description "[Results from the adjusted haplotype-based conditional logistic regression analysis showed a modest association of the PTGER2 2-1-1 haplotype with reduced risk of MI (odds ratio = 0.50, 95% CI; CI = 0.26-0.97, P = 0.04), and the 2-2-1 haplotype with reduced risk of ischemic stroke (odds ratio = 0.68, 95% CI = 0.47-0.99, P = 0.048).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP158096.RAkFGDYQCxecHzjPXkYlcVWgVS98J7vaI1jxz5mvlwHuc130_provenance.
- NP158096.RAkFGDYQCxecHzjPXkYlcVWgVS98J7vaI1jxz5mvlwHuc130_assertion evidence source_evidence_literature NP158096.RAkFGDYQCxecHzjPXkYlcVWgVS98J7vaI1jxz5mvlwHuc130_provenance.
- NP158096.RAkFGDYQCxecHzjPXkYlcVWgVS98J7vaI1jxz5mvlwHuc130_assertion SIO_000772 16879213 NP158096.RAkFGDYQCxecHzjPXkYlcVWgVS98J7vaI1jxz5mvlwHuc130_provenance.
- NP158096.RAkFGDYQCxecHzjPXkYlcVWgVS98J7vaI1jxz5mvlwHuc130_assertion wasDerivedFrom befree-20140225 NP158096.RAkFGDYQCxecHzjPXkYlcVWgVS98J7vaI1jxz5mvlwHuc130_provenance.
- NP158096.RAkFGDYQCxecHzjPXkYlcVWgVS98J7vaI1jxz5mvlwHuc130_assertion wasGeneratedBy ECO_0000203 NP158096.RAkFGDYQCxecHzjPXkYlcVWgVS98J7vaI1jxz5mvlwHuc130_provenance.
- befree-20140225 importedOn "2014-02-25" NP158096.RAkFGDYQCxecHzjPXkYlcVWgVS98J7vaI1jxz5mvlwHuc130_provenance.