Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP222085.RA_kmCOPgxfvotLTftsXIcrWwZ1d-TU6lllO6YmFVC6cw130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP222085.RA_kmCOPgxfvotLTftsXIcrWwZ1d-TU6lllO6YmFVC6cw130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP222085.RA_kmCOPgxfvotLTftsXIcrWwZ1d-TU6lllO6YmFVC6cw130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP222085.RA_kmCOPgxfvotLTftsXIcrWwZ1d-TU6lllO6YmFVC6cw130_provenance.
- NP222085.RA_kmCOPgxfvotLTftsXIcrWwZ1d-TU6lllO6YmFVC6cw130_assertion description "[loss-of-function mutations in genes encoding the cardiac L-type calcium channel to be associated with a familial sudden cardiac death syndrome in which a Brugada syndrome phenotype is combined with shorter-than-normal QT intervals ]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP222085.RA_kmCOPgxfvotLTftsXIcrWwZ1d-TU6lllO6YmFVC6cw130_provenance.
- NP222085.RA_kmCOPgxfvotLTftsXIcrWwZ1d-TU6lllO6YmFVC6cw130_assertion evidence source_evidence_literature NP222085.RA_kmCOPgxfvotLTftsXIcrWwZ1d-TU6lllO6YmFVC6cw130_provenance.
- NP222085.RA_kmCOPgxfvotLTftsXIcrWwZ1d-TU6lllO6YmFVC6cw130_assertion SIO_000772 17224476 NP222085.RA_kmCOPgxfvotLTftsXIcrWwZ1d-TU6lllO6YmFVC6cw130_provenance.
- NP222085.RA_kmCOPgxfvotLTftsXIcrWwZ1d-TU6lllO6YmFVC6cw130_assertion wasDerivedFrom lhgdn-20090331 NP222085.RA_kmCOPgxfvotLTftsXIcrWwZ1d-TU6lllO6YmFVC6cw130_provenance.
- NP222085.RA_kmCOPgxfvotLTftsXIcrWwZ1d-TU6lllO6YmFVC6cw130_assertion wasGeneratedBy ECO_0000203 NP222085.RA_kmCOPgxfvotLTftsXIcrWwZ1d-TU6lllO6YmFVC6cw130_provenance.
- lhgdn-20090331 importedOn "2009-03-31" NP222085.RA_kmCOPgxfvotLTftsXIcrWwZ1d-TU6lllO6YmFVC6cw130_provenance.