Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP683104.RAR6Wro-1LkALW09dGRQlN1g5l0effnzJvQm5KugPz0Ck130_assertion> ?p ?o ?g. }
Showing items 1 to 6 of
6
with 100 items per page.
- NP683104.RAR6Wro-1LkALW09dGRQlN1g5l0effnzJvQm5KugPz0Ck130_assertion type Assertion NP683104.RAR6Wro-1LkALW09dGRQlN1g5l0effnzJvQm5KugPz0Ck130_head.
- NP683104.RAR6Wro-1LkALW09dGRQlN1g5l0effnzJvQm5KugPz0Ck130_assertion description "[Loss-of-function mutations in the gene SCN5A can cause Brugada syndrome (BrS), which is an inherited form of idiopathic ventricular fibrillation.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP683104.RAR6Wro-1LkALW09dGRQlN1g5l0effnzJvQm5KugPz0Ck130_provenance.
- NP683104.RAR6Wro-1LkALW09dGRQlN1g5l0effnzJvQm5KugPz0Ck130_assertion evidence source_evidence_literature NP683104.RAR6Wro-1LkALW09dGRQlN1g5l0effnzJvQm5KugPz0Ck130_provenance.
- NP683104.RAR6Wro-1LkALW09dGRQlN1g5l0effnzJvQm5KugPz0Ck130_assertion SIO_000772 17897138 NP683104.RAR6Wro-1LkALW09dGRQlN1g5l0effnzJvQm5KugPz0Ck130_provenance.
- NP683104.RAR6Wro-1LkALW09dGRQlN1g5l0effnzJvQm5KugPz0Ck130_assertion wasDerivedFrom befree-20150227 NP683104.RAR6Wro-1LkALW09dGRQlN1g5l0effnzJvQm5KugPz0Ck130_provenance.
- NP683104.RAR6Wro-1LkALW09dGRQlN1g5l0effnzJvQm5KugPz0Ck130_assertion wasGeneratedBy ECO_0000203 NP683104.RAR6Wro-1LkALW09dGRQlN1g5l0effnzJvQm5KugPz0Ck130_provenance.