Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP898114.RAvJCOryO2wg564SiSDHiOnzOUWweDW96NlWLifwsMVkc130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP898114.RAvJCOryO2wg564SiSDHiOnzOUWweDW96NlWLifwsMVkc130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP898114.RAvJCOryO2wg564SiSDHiOnzOUWweDW96NlWLifwsMVkc130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP898114.RAvJCOryO2wg564SiSDHiOnzOUWweDW96NlWLifwsMVkc130_provenance.
- NP898114.RAvJCOryO2wg564SiSDHiOnzOUWweDW96NlWLifwsMVkc130_assertion description "[Based on our data, we speculated that the SNP rs8193037 of IL17A gene is significantly associated with CAD risk in Chinese Han population and the rs8193037 G allele which is associated with increased expression of IL17A in AMI patients may be an independent predictive factor for CAD.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP898114.RAvJCOryO2wg564SiSDHiOnzOUWweDW96NlWLifwsMVkc130_provenance.
- NP898114.RAvJCOryO2wg564SiSDHiOnzOUWweDW96NlWLifwsMVkc130_assertion evidence source_evidence_literature NP898114.RAvJCOryO2wg564SiSDHiOnzOUWweDW96NlWLifwsMVkc130_provenance.
- NP898114.RAvJCOryO2wg564SiSDHiOnzOUWweDW96NlWLifwsMVkc130_assertion SIO_000772 21062626 NP898114.RAvJCOryO2wg564SiSDHiOnzOUWweDW96NlWLifwsMVkc130_provenance.
- NP898114.RAvJCOryO2wg564SiSDHiOnzOUWweDW96NlWLifwsMVkc130_assertion wasDerivedFrom befree-20140225 NP898114.RAvJCOryO2wg564SiSDHiOnzOUWweDW96NlWLifwsMVkc130_provenance.
- NP898114.RAvJCOryO2wg564SiSDHiOnzOUWweDW96NlWLifwsMVkc130_assertion wasGeneratedBy ECO_0000203 NP898114.RAvJCOryO2wg564SiSDHiOnzOUWweDW96NlWLifwsMVkc130_provenance.
- befree-20140225 importedOn "2014-02-25" NP898114.RAvJCOryO2wg564SiSDHiOnzOUWweDW96NlWLifwsMVkc130_provenance.