Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP16906.RAfhXVXfkQo2a-NV3lepKYVCmhOB1jmMEUMDvuatpIS08130_assertion> ?p ?o ?g. }
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- NP16906.RAfhXVXfkQo2a-NV3lepKYVCmhOB1jmMEUMDvuatpIS08130_assertion type Assertion NP16906.RAfhXVXfkQo2a-NV3lepKYVCmhOB1jmMEUMDvuatpIS08130_head.
- NP16906.RAfhXVXfkQo2a-NV3lepKYVCmhOB1jmMEUMDvuatpIS08130_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." NP16906.RAfhXVXfkQo2a-NV3lepKYVCmhOB1jmMEUMDvuatpIS08130_provenance.
- NP16906.RAfhXVXfkQo2a-NV3lepKYVCmhOB1jmMEUMDvuatpIS08130_assertion evidence source_evidence_curated NP16906.RAfhXVXfkQo2a-NV3lepKYVCmhOB1jmMEUMDvuatpIS08130_provenance.
- NP16906.RAfhXVXfkQo2a-NV3lepKYVCmhOB1jmMEUMDvuatpIS08130_assertion SIO_000772 23872634 NP16906.RAfhXVXfkQo2a-NV3lepKYVCmhOB1jmMEUMDvuatpIS08130_provenance.
- NP16906.RAfhXVXfkQo2a-NV3lepKYVCmhOB1jmMEUMDvuatpIS08130_assertion wasDerivedFrom ctd_human-20150221 NP16906.RAfhXVXfkQo2a-NV3lepKYVCmhOB1jmMEUMDvuatpIS08130_provenance.
- NP16906.RAfhXVXfkQo2a-NV3lepKYVCmhOB1jmMEUMDvuatpIS08130_assertion wasGeneratedBy ECO_0000218 NP16906.RAfhXVXfkQo2a-NV3lepKYVCmhOB1jmMEUMDvuatpIS08130_provenance.