Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP222084.RAk93zpDUb8ZRGlO7Zzlfww7e_RSMyzZ-CnIcnICX0crc130_assertion> ?p ?o ?g. }
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- NP222084.RAk93zpDUb8ZRGlO7Zzlfww7e_RSMyzZ-CnIcnICX0crc130_assertion type Assertion NP222084.RAk93zpDUb8ZRGlO7Zzlfww7e_RSMyzZ-CnIcnICX0crc130_head.
- NP222084.RAk93zpDUb8ZRGlO7Zzlfww7e_RSMyzZ-CnIcnICX0crc130_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." NP222084.RAk93zpDUb8ZRGlO7Zzlfww7e_RSMyzZ-CnIcnICX0crc130_provenance.
- NP222084.RAk93zpDUb8ZRGlO7Zzlfww7e_RSMyzZ-CnIcnICX0crc130_assertion evidence source_evidence_literature NP222084.RAk93zpDUb8ZRGlO7Zzlfww7e_RSMyzZ-CnIcnICX0crc130_provenance.
- NP222084.RAk93zpDUb8ZRGlO7Zzlfww7e_RSMyzZ-CnIcnICX0crc130_assertion SIO_000772 17224476 NP222084.RAk93zpDUb8ZRGlO7Zzlfww7e_RSMyzZ-CnIcnICX0crc130_provenance.
- NP222084.RAk93zpDUb8ZRGlO7Zzlfww7e_RSMyzZ-CnIcnICX0crc130_assertion wasDerivedFrom lhgdn-20090331 NP222084.RAk93zpDUb8ZRGlO7Zzlfww7e_RSMyzZ-CnIcnICX0crc130_provenance.
- NP222084.RAk93zpDUb8ZRGlO7Zzlfww7e_RSMyzZ-CnIcnICX0crc130_assertion wasGeneratedBy ECO_0000203 NP222084.RAk93zpDUb8ZRGlO7Zzlfww7e_RSMyzZ-CnIcnICX0crc130_provenance.