Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP490626.RAhmF6022PNsLH_iCoZ-EaHx4BSoeRc04wu1K3K88ve7Y130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP490626.RAhmF6022PNsLH_iCoZ-EaHx4BSoeRc04wu1K3K88ve7Y130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP490626.RAhmF6022PNsLH_iCoZ-EaHx4BSoeRc04wu1K3K88ve7Y130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP490626.RAhmF6022PNsLH_iCoZ-EaHx4BSoeRc04wu1K3K88ve7Y130_provenance.
- befree-2016 importedOn "2016-02-19" NP490626.RAhmF6022PNsLH_iCoZ-EaHx4BSoeRc04wu1K3K88ve7Y130_provenance.
- NP490626.RAhmF6022PNsLH_iCoZ-EaHx4BSoeRc04wu1K3K88ve7Y130_assertion wasGeneratedBy ECO_0000203 NP490626.RAhmF6022PNsLH_iCoZ-EaHx4BSoeRc04wu1K3K88ve7Y130_provenance.
- NP490626.RAhmF6022PNsLH_iCoZ-EaHx4BSoeRc04wu1K3K88ve7Y130_assertion wasDerivedFrom befree-2016 NP490626.RAhmF6022PNsLH_iCoZ-EaHx4BSoeRc04wu1K3K88ve7Y130_provenance.
- NP490626.RAhmF6022PNsLH_iCoZ-EaHx4BSoeRc04wu1K3K88ve7Y130_assertion SIO_000772 15838369 NP490626.RAhmF6022PNsLH_iCoZ-EaHx4BSoeRc04wu1K3K88ve7Y130_provenance.
- NP490626.RAhmF6022PNsLH_iCoZ-EaHx4BSoeRc04wu1K3K88ve7Y130_assertion evidence source_evidence_literature NP490626.RAhmF6022PNsLH_iCoZ-EaHx4BSoeRc04wu1K3K88ve7Y130_provenance.
- NP490626.RAhmF6022PNsLH_iCoZ-EaHx4BSoeRc04wu1K3K88ve7Y130_assertion description "[All our results indicate that the presence of the ET-1 genotype (++) in patients with structural heart disease, severe left ventricular dysfunction and malignant ventricular arrhythmias increases the risk for these patients of hemodynamic collapse during these arrhythmias.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP490626.RAhmF6022PNsLH_iCoZ-EaHx4BSoeRc04wu1K3K88ve7Y130_provenance.