Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP851357.RAvUbmhnO6vqHxVbq-i-YLZQSof9qQ8cZpMtmu20JzehE130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP851357.RAvUbmhnO6vqHxVbq-i-YLZQSof9qQ8cZpMtmu20JzehE130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP851357.RAvUbmhnO6vqHxVbq-i-YLZQSof9qQ8cZpMtmu20JzehE130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP851357.RAvUbmhnO6vqHxVbq-i-YLZQSof9qQ8cZpMtmu20JzehE130_provenance.
- NP851357.RAvUbmhnO6vqHxVbq-i-YLZQSof9qQ8cZpMtmu20JzehE130_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." NP851357.RAvUbmhnO6vqHxVbq-i-YLZQSof9qQ8cZpMtmu20JzehE130_provenance.
- NP851357.RAvUbmhnO6vqHxVbq-i-YLZQSof9qQ8cZpMtmu20JzehE130_assertion evidence source_evidence_literature NP851357.RAvUbmhnO6vqHxVbq-i-YLZQSof9qQ8cZpMtmu20JzehE130_provenance.
- NP851357.RAvUbmhnO6vqHxVbq-i-YLZQSof9qQ8cZpMtmu20JzehE130_assertion SIO_000772 21062626 NP851357.RAvUbmhnO6vqHxVbq-i-YLZQSof9qQ8cZpMtmu20JzehE130_provenance.
- NP851357.RAvUbmhnO6vqHxVbq-i-YLZQSof9qQ8cZpMtmu20JzehE130_assertion wasDerivedFrom befree-2016 NP851357.RAvUbmhnO6vqHxVbq-i-YLZQSof9qQ8cZpMtmu20JzehE130_provenance.
- NP851357.RAvUbmhnO6vqHxVbq-i-YLZQSof9qQ8cZpMtmu20JzehE130_assertion wasGeneratedBy ECO_0000203 NP851357.RAvUbmhnO6vqHxVbq-i-YLZQSof9qQ8cZpMtmu20JzehE130_provenance.
- befree-2016 importedOn "2016-02-19" NP851357.RAvUbmhnO6vqHxVbq-i-YLZQSof9qQ8cZpMtmu20JzehE130_provenance.