Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP1171498.RAn8KahIG35pamSQKQF2hULeHUjpx--JBw0Jwb_bzBA1s130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP1171498.RAn8KahIG35pamSQKQF2hULeHUjpx--JBw0Jwb_bzBA1s130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP1171498.RAn8KahIG35pamSQKQF2hULeHUjpx--JBw0Jwb_bzBA1s130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP1171498.RAn8KahIG35pamSQKQF2hULeHUjpx--JBw0Jwb_bzBA1s130_provenance.
- NP1171498.RAn8KahIG35pamSQKQF2hULeHUjpx--JBw0Jwb_bzBA1s130_assertion description "[We aimed to comprehensively investigate which NOS gene variants are most strongly associated with coronary heart disease (CHD) and hypertension, using a set of tagging SNPs with good coverage across the 3 genes.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1171498.RAn8KahIG35pamSQKQF2hULeHUjpx--JBw0Jwb_bzBA1s130_provenance.
- NP1171498.RAn8KahIG35pamSQKQF2hULeHUjpx--JBw0Jwb_bzBA1s130_assertion evidence source_evidence_literature NP1171498.RAn8KahIG35pamSQKQF2hULeHUjpx--JBw0Jwb_bzBA1s130_provenance.
- NP1171498.RAn8KahIG35pamSQKQF2hULeHUjpx--JBw0Jwb_bzBA1s130_assertion SIO_000772 24713495 NP1171498.RAn8KahIG35pamSQKQF2hULeHUjpx--JBw0Jwb_bzBA1s130_provenance.
- NP1171498.RAn8KahIG35pamSQKQF2hULeHUjpx--JBw0Jwb_bzBA1s130_assertion wasDerivedFrom befree-2016 NP1171498.RAn8KahIG35pamSQKQF2hULeHUjpx--JBw0Jwb_bzBA1s130_provenance.
- NP1171498.RAn8KahIG35pamSQKQF2hULeHUjpx--JBw0Jwb_bzBA1s130_assertion wasGeneratedBy ECO_0000203 NP1171498.RAn8KahIG35pamSQKQF2hULeHUjpx--JBw0Jwb_bzBA1s130_provenance.
- befree-2016 importedOn "2016-02-19" NP1171498.RAn8KahIG35pamSQKQF2hULeHUjpx--JBw0Jwb_bzBA1s130_provenance.