Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP29150.RAPBiDZFiApdw9SKOSWoEbg_Z5qYlH_4vy0jXAWyBEX_E130_assertion> ?p ?o ?g. }
Showing items 1 to 6 of
6
with 100 items per page.
- NP29150.RAPBiDZFiApdw9SKOSWoEbg_Z5qYlH_4vy0jXAWyBEX_E130_assertion type Assertion NP29150.RAPBiDZFiApdw9SKOSWoEbg_Z5qYlH_4vy0jXAWyBEX_E130_head.
- NP29150.RAPBiDZFiApdw9SKOSWoEbg_Z5qYlH_4vy0jXAWyBEX_E130_assertion description "[Loss-of-function mutations in SCN5A, the gene encoding Na(v)1.5 Na+ channel, are associated with inherited cardiac conduction defects and Brugada syndrome, which both exhibit variable phenotypic penetrance of conduction defects.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP29150.RAPBiDZFiApdw9SKOSWoEbg_Z5qYlH_4vy0jXAWyBEX_E130_provenance.
- NP29150.RAPBiDZFiApdw9SKOSWoEbg_Z5qYlH_4vy0jXAWyBEX_E130_assertion evidence source_evidence_curated NP29150.RAPBiDZFiApdw9SKOSWoEbg_Z5qYlH_4vy0jXAWyBEX_E130_provenance.
- NP29150.RAPBiDZFiApdw9SKOSWoEbg_Z5qYlH_4vy0jXAWyBEX_E130_assertion SIO_000772 20174578 NP29150.RAPBiDZFiApdw9SKOSWoEbg_Z5qYlH_4vy0jXAWyBEX_E130_provenance.
- NP29150.RAPBiDZFiApdw9SKOSWoEbg_Z5qYlH_4vy0jXAWyBEX_E130_assertion wasDerivedFrom ctd_human-20150221 NP29150.RAPBiDZFiApdw9SKOSWoEbg_Z5qYlH_4vy0jXAWyBEX_E130_provenance.
- NP29150.RAPBiDZFiApdw9SKOSWoEbg_Z5qYlH_4vy0jXAWyBEX_E130_assertion wasGeneratedBy ECO_0000218 NP29150.RAPBiDZFiApdw9SKOSWoEbg_Z5qYlH_4vy0jXAWyBEX_E130_provenance.