Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP29149.RAggcaV1fBX9wxg4AJgtRs9Go38BeiMRVTOICz_Vspxqw130_assertion> ?p ?o ?g. }
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- NP29149.RAggcaV1fBX9wxg4AJgtRs9Go38BeiMRVTOICz_Vspxqw130_assertion type Assertion NP29149.RAggcaV1fBX9wxg4AJgtRs9Go38BeiMRVTOICz_Vspxqw130_head.
- NP29149.RAggcaV1fBX9wxg4AJgtRs9Go38BeiMRVTOICz_Vspxqw130_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." NP29149.RAggcaV1fBX9wxg4AJgtRs9Go38BeiMRVTOICz_Vspxqw130_provenance.
- NP29149.RAggcaV1fBX9wxg4AJgtRs9Go38BeiMRVTOICz_Vspxqw130_assertion evidence source_evidence_curated NP29149.RAggcaV1fBX9wxg4AJgtRs9Go38BeiMRVTOICz_Vspxqw130_provenance.
- NP29149.RAggcaV1fBX9wxg4AJgtRs9Go38BeiMRVTOICz_Vspxqw130_assertion SIO_000772 23872634 NP29149.RAggcaV1fBX9wxg4AJgtRs9Go38BeiMRVTOICz_Vspxqw130_provenance.
- NP29149.RAggcaV1fBX9wxg4AJgtRs9Go38BeiMRVTOICz_Vspxqw130_assertion wasDerivedFrom ctd_human-20150221 NP29149.RAggcaV1fBX9wxg4AJgtRs9Go38BeiMRVTOICz_Vspxqw130_provenance.
- NP29149.RAggcaV1fBX9wxg4AJgtRs9Go38BeiMRVTOICz_Vspxqw130_assertion wasGeneratedBy ECO_0000218 NP29149.RAggcaV1fBX9wxg4AJgtRs9Go38BeiMRVTOICz_Vspxqw130_provenance.