Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP205315.RA4uSFVo4xon3kwXX26aGillILnkWafJ_7Gso4km3P848130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP205315.RA4uSFVo4xon3kwXX26aGillILnkWafJ_7Gso4km3P848130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP205315.RA4uSFVo4xon3kwXX26aGillILnkWafJ_7Gso4km3P848130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP205315.RA4uSFVo4xon3kwXX26aGillILnkWafJ_7Gso4km3P848130_provenance.
- NP205315.RA4uSFVo4xon3kwXX26aGillILnkWafJ_7Gso4km3P848130_assertion description "[The CFH 402H allele was associated with an increased risk for incident CHD and ischemic stroke in whites, with the strength and significance of the association dependent upon hypertension status.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP205315.RA4uSFVo4xon3kwXX26aGillILnkWafJ_7Gso4km3P848130_provenance.
- NP205315.RA4uSFVo4xon3kwXX26aGillILnkWafJ_7Gso4km3P848130_assertion evidence source_evidence_literature NP205315.RA4uSFVo4xon3kwXX26aGillILnkWafJ_7Gso4km3P848130_provenance.
- NP205315.RA4uSFVo4xon3kwXX26aGillILnkWafJ_7Gso4km3P848130_assertion SIO_000772 18292760 NP205315.RA4uSFVo4xon3kwXX26aGillILnkWafJ_7Gso4km3P848130_provenance.
- NP205315.RA4uSFVo4xon3kwXX26aGillILnkWafJ_7Gso4km3P848130_assertion wasDerivedFrom befree-20140225 NP205315.RA4uSFVo4xon3kwXX26aGillILnkWafJ_7Gso4km3P848130_provenance.
- NP205315.RA4uSFVo4xon3kwXX26aGillILnkWafJ_7Gso4km3P848130_assertion wasGeneratedBy ECO_0000203 NP205315.RA4uSFVo4xon3kwXX26aGillILnkWafJ_7Gso4km3P848130_provenance.
- befree-20140225 importedOn "2014-02-25" NP205315.RA4uSFVo4xon3kwXX26aGillILnkWafJ_7Gso4km3P848130_provenance.