Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP210387.RAXSmZzC23WpSe2T4I-vmhDh5p2-rXZagvmbXWLn0tpMY130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP210387.RAXSmZzC23WpSe2T4I-vmhDh5p2-rXZagvmbXWLn0tpMY130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP210387.RAXSmZzC23WpSe2T4I-vmhDh5p2-rXZagvmbXWLn0tpMY130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP210387.RAXSmZzC23WpSe2T4I-vmhDh5p2-rXZagvmbXWLn0tpMY130_provenance.
- lhgdn-20090331 importedOn "2009-03-31" NP210387.RAXSmZzC23WpSe2T4I-vmhDh5p2-rXZagvmbXWLn0tpMY130_provenance.
- NP210387.RAXSmZzC23WpSe2T4I-vmhDh5p2-rXZagvmbXWLn0tpMY130_assertion wasGeneratedBy ECO_0000203 NP210387.RAXSmZzC23WpSe2T4I-vmhDh5p2-rXZagvmbXWLn0tpMY130_provenance.
- NP210387.RAXSmZzC23WpSe2T4I-vmhDh5p2-rXZagvmbXWLn0tpMY130_assertion wasDerivedFrom lhgdn-20090331 NP210387.RAXSmZzC23WpSe2T4I-vmhDh5p2-rXZagvmbXWLn0tpMY130_provenance.
- NP210387.RAXSmZzC23WpSe2T4I-vmhDh5p2-rXZagvmbXWLn0tpMY130_assertion SIO_000772 15838369 NP210387.RAXSmZzC23WpSe2T4I-vmhDh5p2-rXZagvmbXWLn0tpMY130_provenance.
- NP210387.RAXSmZzC23WpSe2T4I-vmhDh5p2-rXZagvmbXWLn0tpMY130_assertion evidence source_evidence_literature NP210387.RAXSmZzC23WpSe2T4I-vmhDh5p2-rXZagvmbXWLn0tpMY130_provenance.
- NP210387.RAXSmZzC23WpSe2T4I-vmhDh5p2-rXZagvmbXWLn0tpMY130_assertion description "[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." NP210387.RAXSmZzC23WpSe2T4I-vmhDh5p2-rXZagvmbXWLn0tpMY130_provenance.