Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP531185.RASqiszRRZlM2l9slQ3r3c8p2opTY9oINe2mkkLcCs5P0130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP531185.RASqiszRRZlM2l9slQ3r3c8p2opTY9oINe2mkkLcCs5P0130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP531185.RASqiszRRZlM2l9slQ3r3c8p2opTY9oINe2mkkLcCs5P0130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP531185.RASqiszRRZlM2l9slQ3r3c8p2opTY9oINe2mkkLcCs5P0130_provenance.
- NP531185.RASqiszRRZlM2l9slQ3r3c8p2opTY9oINe2mkkLcCs5P0130_assertion description "[Loss of function mutations in SCN5A, encoding the cardiac sodium channel, are one cause of the Brugada syndrome, associated with slow conduction and a high incidence of ventricular fibrillation, especially in Asians.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP531185.RASqiszRRZlM2l9slQ3r3c8p2opTY9oINe2mkkLcCs5P0130_provenance.
- NP531185.RASqiszRRZlM2l9slQ3r3c8p2opTY9oINe2mkkLcCs5P0130_assertion evidence source_evidence_literature NP531185.RASqiszRRZlM2l9slQ3r3c8p2opTY9oINe2mkkLcCs5P0130_provenance.
- NP531185.RASqiszRRZlM2l9slQ3r3c8p2opTY9oINe2mkkLcCs5P0130_assertion SIO_000772 16415376 NP531185.RASqiszRRZlM2l9slQ3r3c8p2opTY9oINe2mkkLcCs5P0130_provenance.
- NP531185.RASqiszRRZlM2l9slQ3r3c8p2opTY9oINe2mkkLcCs5P0130_assertion wasDerivedFrom befree-2016 NP531185.RASqiszRRZlM2l9slQ3r3c8p2opTY9oINe2mkkLcCs5P0130_provenance.
- NP531185.RASqiszRRZlM2l9slQ3r3c8p2opTY9oINe2mkkLcCs5P0130_assertion wasGeneratedBy ECO_0000203 NP531185.RASqiszRRZlM2l9slQ3r3c8p2opTY9oINe2mkkLcCs5P0130_provenance.
- befree-2016 importedOn "2016-02-19" NP531185.RASqiszRRZlM2l9slQ3r3c8p2opTY9oINe2mkkLcCs5P0130_provenance.