Matches in Nanopublications for { <http://rdf.disgenet.org/nanopublications.trig#NP847756.RAmm2F8PZvsh9qV_pmQPEx9MuKs6Cg_drVt27IDHbATws130_assertion> ?p ?o ?g. }
Showing items 1 to 6 of
6
with 100 items per page.
- NP847756.RAmm2F8PZvsh9qV_pmQPEx9MuKs6Cg_drVt27IDHbATws130_assertion type Assertion NP847756.RAmm2F8PZvsh9qV_pmQPEx9MuKs6Cg_drVt27IDHbATws130_head.
- NP847756.RAmm2F8PZvsh9qV_pmQPEx9MuKs6Cg_drVt27IDHbATws130_assertion description "[Common variants at SCN5A-SCN10A and HEY2 are associated with Brugada syndrome, a rare disease with high risk of sudden cardiac death.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP847756.RAmm2F8PZvsh9qV_pmQPEx9MuKs6Cg_drVt27IDHbATws130_provenance.
- NP847756.RAmm2F8PZvsh9qV_pmQPEx9MuKs6Cg_drVt27IDHbATws130_assertion evidence source_evidence_literature NP847756.RAmm2F8PZvsh9qV_pmQPEx9MuKs6Cg_drVt27IDHbATws130_provenance.
- NP847756.RAmm2F8PZvsh9qV_pmQPEx9MuKs6Cg_drVt27IDHbATws130_assertion SIO_000772 23872634 NP847756.RAmm2F8PZvsh9qV_pmQPEx9MuKs6Cg_drVt27IDHbATws130_provenance.
- NP847756.RAmm2F8PZvsh9qV_pmQPEx9MuKs6Cg_drVt27IDHbATws130_assertion wasDerivedFrom befree-20140225 NP847756.RAmm2F8PZvsh9qV_pmQPEx9MuKs6Cg_drVt27IDHbATws130_provenance.
- NP847756.RAmm2F8PZvsh9qV_pmQPEx9MuKs6Cg_drVt27IDHbATws130_assertion wasGeneratedBy ECO_0000203 NP847756.RAmm2F8PZvsh9qV_pmQPEx9MuKs6Cg_drVt27IDHbATws130_provenance.