Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP16906.RAfhXVXfkQo2a-NV3lepKYVCmhOB1jmMEUMDvuatpIS08130_provenance>. }
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- source_evidence_curated type ECO_0000205 NP16906.RAfhXVXfkQo2a-NV3lepKYVCmhOB1jmMEUMDvuatpIS08130_provenance.
- source_evidence_curated label "DisGeNET evidence - CURATED" NP16906.RAfhXVXfkQo2a-NV3lepKYVCmhOB1jmMEUMDvuatpIS08130_provenance.
- source_evidence_curated comment "Gene-disease associations manually curated." NP16906.RAfhXVXfkQo2a-NV3lepKYVCmhOB1jmMEUMDvuatpIS08130_provenance.
- 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.
- ctd_human-20150221 importedOn "2015-02-21" NP16906.RAfhXVXfkQo2a-NV3lepKYVCmhOB1jmMEUMDvuatpIS08130_provenance.