Matches in Nanopublications for { <http://rdf.disgenet.org/nanopublications.trig#NP134529.RAXDDFfmVGRX-e0BOV5TffY2LXrLIfDTmjt6MwLzerktM130_assertion> ?p ?o ?g. }
Showing items 1 to 6 of
6
with 100 items per page.
- NP134529.RAXDDFfmVGRX-e0BOV5TffY2LXrLIfDTmjt6MwLzerktM130_assertion type Assertion NP134529.RAXDDFfmVGRX-e0BOV5TffY2LXrLIfDTmjt6MwLzerktM130_head.
- NP134529.RAXDDFfmVGRX-e0BOV5TffY2LXrLIfDTmjt6MwLzerktM130_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." NP134529.RAXDDFfmVGRX-e0BOV5TffY2LXrLIfDTmjt6MwLzerktM130_provenance.
- NP134529.RAXDDFfmVGRX-e0BOV5TffY2LXrLIfDTmjt6MwLzerktM130_assertion evidence source_evidence_literature NP134529.RAXDDFfmVGRX-e0BOV5TffY2LXrLIfDTmjt6MwLzerktM130_provenance.
- NP134529.RAXDDFfmVGRX-e0BOV5TffY2LXrLIfDTmjt6MwLzerktM130_assertion SIO_000772 17224476 NP134529.RAXDDFfmVGRX-e0BOV5TffY2LXrLIfDTmjt6MwLzerktM130_provenance.
- NP134529.RAXDDFfmVGRX-e0BOV5TffY2LXrLIfDTmjt6MwLzerktM130_assertion wasDerivedFrom lhgdn-20090331 NP134529.RAXDDFfmVGRX-e0BOV5TffY2LXrLIfDTmjt6MwLzerktM130_provenance.
- NP134529.RAXDDFfmVGRX-e0BOV5TffY2LXrLIfDTmjt6MwLzerktM130_assertion wasGeneratedBy ECO_0000203 NP134529.RAXDDFfmVGRX-e0BOV5TffY2LXrLIfDTmjt6MwLzerktM130_provenance.