Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP531186.RAiM27D9OBlhCvMBwKVEKFc2Kd1vLe4WITmxguJZsvO74130_assertion> ?p ?o ?g. }
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- NP531186.RAiM27D9OBlhCvMBwKVEKFc2Kd1vLe4WITmxguJZsvO74130_assertion type Assertion NP531186.RAiM27D9OBlhCvMBwKVEKFc2Kd1vLe4WITmxguJZsvO74130_head.
- NP531186.RAiM27D9OBlhCvMBwKVEKFc2Kd1vLe4WITmxguJZsvO74130_assertion description "[Loss of function mutations in SCN5A, encoding the cardiac sodium channel, are one cause of the Brugada syndrome, associated with slow conduction and a high incidence of ventricular fibrillation, especially in Asians.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP531186.RAiM27D9OBlhCvMBwKVEKFc2Kd1vLe4WITmxguJZsvO74130_provenance.
- NP531186.RAiM27D9OBlhCvMBwKVEKFc2Kd1vLe4WITmxguJZsvO74130_assertion evidence source_evidence_literature NP531186.RAiM27D9OBlhCvMBwKVEKFc2Kd1vLe4WITmxguJZsvO74130_provenance.
- NP531186.RAiM27D9OBlhCvMBwKVEKFc2Kd1vLe4WITmxguJZsvO74130_assertion SIO_000772 16415376 NP531186.RAiM27D9OBlhCvMBwKVEKFc2Kd1vLe4WITmxguJZsvO74130_provenance.
- NP531186.RAiM27D9OBlhCvMBwKVEKFc2Kd1vLe4WITmxguJZsvO74130_assertion wasDerivedFrom befree-2016 NP531186.RAiM27D9OBlhCvMBwKVEKFc2Kd1vLe4WITmxguJZsvO74130_provenance.
- NP531186.RAiM27D9OBlhCvMBwKVEKFc2Kd1vLe4WITmxguJZsvO74130_assertion wasGeneratedBy ECO_0000203 NP531186.RAiM27D9OBlhCvMBwKVEKFc2Kd1vLe4WITmxguJZsvO74130_provenance.