Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP216813.RAQC3vxXeaMqhq59MaeGk7FnmxIa6ppkF46cXPFjrYjEA130_assertion> ?p ?o ?g. }
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- NP216813.RAQC3vxXeaMqhq59MaeGk7FnmxIa6ppkF46cXPFjrYjEA130_assertion type Assertion NP216813.RAQC3vxXeaMqhq59MaeGk7FnmxIa6ppkF46cXPFjrYjEA130_head.
- NP216813.RAQC3vxXeaMqhq59MaeGk7FnmxIa6ppkF46cXPFjrYjEA130_assertion description "[loss-of-function mutations in genes encoding the cardiac L-type calcium channel to be associated with a familial sudden cardiac death syndrome in which a Brugada syndrome phenotype is combined with shorter-than-normal QT intervals ]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP216813.RAQC3vxXeaMqhq59MaeGk7FnmxIa6ppkF46cXPFjrYjEA130_provenance.
- NP216813.RAQC3vxXeaMqhq59MaeGk7FnmxIa6ppkF46cXPFjrYjEA130_assertion evidence source_evidence_literature NP216813.RAQC3vxXeaMqhq59MaeGk7FnmxIa6ppkF46cXPFjrYjEA130_provenance.
- NP216813.RAQC3vxXeaMqhq59MaeGk7FnmxIa6ppkF46cXPFjrYjEA130_assertion SIO_000772 17224476 NP216813.RAQC3vxXeaMqhq59MaeGk7FnmxIa6ppkF46cXPFjrYjEA130_provenance.
- NP216813.RAQC3vxXeaMqhq59MaeGk7FnmxIa6ppkF46cXPFjrYjEA130_assertion wasDerivedFrom lhgdn-20090331 NP216813.RAQC3vxXeaMqhq59MaeGk7FnmxIa6ppkF46cXPFjrYjEA130_provenance.
- NP216813.RAQC3vxXeaMqhq59MaeGk7FnmxIa6ppkF46cXPFjrYjEA130_assertion wasGeneratedBy ECO_0000203 NP216813.RAQC3vxXeaMqhq59MaeGk7FnmxIa6ppkF46cXPFjrYjEA130_provenance.