Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP29106.RA0_NSClgeDP4Alquc-aWNW6yFiLFEU31isiht-RQZAfk130_assertion> ?p ?o ?g. }
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- NP29106.RA0_NSClgeDP4Alquc-aWNW6yFiLFEU31isiht-RQZAfk130_assertion type Assertion NP29106.RA0_NSClgeDP4Alquc-aWNW6yFiLFEU31isiht-RQZAfk130_head.
- NP29106.RA0_NSClgeDP4Alquc-aWNW6yFiLFEU31isiht-RQZAfk130_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." NP29106.RA0_NSClgeDP4Alquc-aWNW6yFiLFEU31isiht-RQZAfk130_provenance.
- NP29106.RA0_NSClgeDP4Alquc-aWNW6yFiLFEU31isiht-RQZAfk130_assertion evidence source_evidence_curated NP29106.RA0_NSClgeDP4Alquc-aWNW6yFiLFEU31isiht-RQZAfk130_provenance.
- NP29106.RA0_NSClgeDP4Alquc-aWNW6yFiLFEU31isiht-RQZAfk130_assertion SIO_000772 23872634 NP29106.RA0_NSClgeDP4Alquc-aWNW6yFiLFEU31isiht-RQZAfk130_provenance.
- NP29106.RA0_NSClgeDP4Alquc-aWNW6yFiLFEU31isiht-RQZAfk130_assertion wasDerivedFrom ctd_human-20150221 NP29106.RA0_NSClgeDP4Alquc-aWNW6yFiLFEU31isiht-RQZAfk130_provenance.
- NP29106.RA0_NSClgeDP4Alquc-aWNW6yFiLFEU31isiht-RQZAfk130_assertion wasGeneratedBy ECO_0000218 NP29106.RA0_NSClgeDP4Alquc-aWNW6yFiLFEU31isiht-RQZAfk130_provenance.