Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP364660.RA4E_nNhL57uRnTTd7-BE5yZNxHRzk6G1EarbVESu29-E130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP364660.RA4E_nNhL57uRnTTd7-BE5yZNxHRzk6G1EarbVESu29-E130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP364660.RA4E_nNhL57uRnTTd7-BE5yZNxHRzk6G1EarbVESu29-E130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP364660.RA4E_nNhL57uRnTTd7-BE5yZNxHRzk6G1EarbVESu29-E130_provenance.
- befree-20150227 importedOn "2015-02-27" NP364660.RA4E_nNhL57uRnTTd7-BE5yZNxHRzk6G1EarbVESu29-E130_provenance.
- NP364660.RA4E_nNhL57uRnTTd7-BE5yZNxHRzk6G1EarbVESu29-E130_assertion wasGeneratedBy ECO_0000203 NP364660.RA4E_nNhL57uRnTTd7-BE5yZNxHRzk6G1EarbVESu29-E130_provenance.
- NP364660.RA4E_nNhL57uRnTTd7-BE5yZNxHRzk6G1EarbVESu29-E130_assertion wasDerivedFrom befree-20150227 NP364660.RA4E_nNhL57uRnTTd7-BE5yZNxHRzk6G1EarbVESu29-E130_provenance.
- NP364660.RA4E_nNhL57uRnTTd7-BE5yZNxHRzk6G1EarbVESu29-E130_assertion SIO_000772 15838369 NP364660.RA4E_nNhL57uRnTTd7-BE5yZNxHRzk6G1EarbVESu29-E130_provenance.
- NP364660.RA4E_nNhL57uRnTTd7-BE5yZNxHRzk6G1EarbVESu29-E130_assertion evidence source_evidence_literature NP364660.RA4E_nNhL57uRnTTd7-BE5yZNxHRzk6G1EarbVESu29-E130_provenance.
- NP364660.RA4E_nNhL57uRnTTd7-BE5yZNxHRzk6G1EarbVESu29-E130_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." NP364660.RA4E_nNhL57uRnTTd7-BE5yZNxHRzk6G1EarbVESu29-E130_provenance.