Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP847756.RAmm2F8PZvsh9qV_pmQPEx9MuKs6Cg_drVt27IDHbATws130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP847756.RAmm2F8PZvsh9qV_pmQPEx9MuKs6Cg_drVt27IDHbATws130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP847756.RAmm2F8PZvsh9qV_pmQPEx9MuKs6Cg_drVt27IDHbATws130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP847756.RAmm2F8PZvsh9qV_pmQPEx9MuKs6Cg_drVt27IDHbATws130_provenance.
- 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.
- befree-20140225 importedOn "2014-02-25" NP847756.RAmm2F8PZvsh9qV_pmQPEx9MuKs6Cg_drVt27IDHbATws130_provenance.