@prefix this: <http://rdf.disgenet.org/resource/nanopub/NP683226.RAAsZlRx_TAPc-SW_Lmuq6uznIa9VRnqhqe3ixUxftHZs> .
@prefix rdfs: <http://www.w3.org/2000/01/rdf-schema#> .
@prefix xsd: <http://www.w3.org/2001/XMLSchema#> .
@prefix sio: <http://semanticscience.org/resource/> .
@prefix ncit: <http://ncicb.nci.nih.gov/xml/owl/EVS/Thesaurus.owl#> .
@prefix lld: <http://linkedlifedata.com/resource/umls/id/> .
@prefix miriam-gene: <http://identifiers.org/ncbigene/> .
@prefix miriam-pubmed: <http://identifiers.org/pubmed/> .
@prefix eco: <http://purl.obolibrary.org/obo/> .
@prefix wi: <http://purl.org/ontology/wi/core#> .
@prefix prov: <http://www.w3.org/ns/prov#> .
@prefix pav: <http://purl.org/pav/> .
@prefix prv: <http://purl.org/net/provenance/ns#> .
@prefix dcterms: <http://purl.org/dc/terms/> .
@prefix np: <http://www.nanopub.org/nschema#> .
@prefix dgn-np: <http://rdf.disgenet.org/resource/nanopub/> .
@prefix dgn-gda: <http://rdf.disgenet.org/resource/gda/> .
@prefix dgn-void: <http://rdf.disgenet.org/v3.0.0/void/> .
dgn-np:NP683226.RAAsZlRx_TAPc-SW_Lmuq6uznIa9VRnqhqe3ixUxftHZs130_head {
  this: np:hasAssertion dgn-np:NP683226.RAAsZlRx_TAPc-SW_Lmuq6uznIa9VRnqhqe3ixUxftHZs130_assertion ;
    np:hasProvenance dgn-np:NP683226.RAAsZlRx_TAPc-SW_Lmuq6uznIa9VRnqhqe3ixUxftHZs130_provenance ;
    np:hasPublicationInfo dgn-np:NP683226.RAAsZlRx_TAPc-SW_Lmuq6uznIa9VRnqhqe3ixUxftHZs130_publicationInfo ;
    a np:Nanopublication .
  dgn-np:NP683226.RAAsZlRx_TAPc-SW_Lmuq6uznIa9VRnqhqe3ixUxftHZs130_assertion a np:Assertion .
  dgn-np:NP683226.RAAsZlRx_TAPc-SW_Lmuq6uznIa9VRnqhqe3ixUxftHZs130_provenance a np:Provenance .
  dgn-np:NP683226.RAAsZlRx_TAPc-SW_Lmuq6uznIa9VRnqhqe3ixUxftHZs130_publicationInfo a np:PublicationInfo .
}
dgn-np:NP683226.RAAsZlRx_TAPc-SW_Lmuq6uznIa9VRnqhqe3ixUxftHZs130_assertion {
  miriam-gene:6331 a ncit:C16612 .
  lld:C2732979 a ncit:C7057 .
  dgn-gda:DGN45d2162b089a553e8087f0dd3175165f sio:SIO_000628 miriam-gene:6331 , lld:C2732979 ;
    a sio:SIO_001121 .
}
dgn-np:NP683226.RAAsZlRx_TAPc-SW_Lmuq6uznIa9VRnqhqe3ixUxftHZs130_provenance {
  dgn-np:NP683226.RAAsZlRx_TAPc-SW_Lmuq6uznIa9VRnqhqe3ixUxftHZs130_assertion dcterms:description "[Mutations in SCN5A, the gene encoding Na(v)1.5, have been linked to many cardiac phenotypes, including the congenital and acquired long QT syndrome, Brugada syndrome, conduction slowing, sick sinus syndrome, atrial fibrillation, and dilated cardiomyopathy.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine."@en ;
    wi:evidence dgn-void:source_evidence_literature ;
    sio:SIO_000772 miriam-pubmed:19744495 ;
    prov:wasDerivedFrom dgn-void:befree-20150227 ;
    prov:wasGeneratedBy eco:ECO_0000203 .
  dgn-void:befree-20150227 pav:importedOn "2015-02-27"^^xsd:date .
  dgn-void:source_evidence_literature a eco:ECO_0000212 ;
    rdfs:comment "Gene-disease associations inferred from text-mining the literature."@en ;
    rdfs:label "DisGeNET evidence - LITERATURE"@en .
}
dgn-np:NP683226.RAAsZlRx_TAPc-SW_Lmuq6uznIa9VRnqhqe3ixUxftHZs130_publicationInfo {
  this: dcterms:created "2015-08-25T14:44:32+02:00"^^xsd:dateTime ;
    dcterms:rights <http://opendatacommons.org/licenses/odbl/1.0/> ;
    dcterms:rightsHolder dgn-void:IBIGroup ;
    dcterms:subject sio:SIO_000983 ;
    prv:usedData dgn-void:disgenetv3.0rdf ;
    pav:authoredBy <http://orcid.org/0000-0001-5999-6269> , <http://orcid.org/0000-0002-7534-7661> , <http://orcid.org/0000-0002-9383-528X> , <http://orcid.org/0000-0003-0169-8159> , <http://orcid.org/0000-0003-1244-7654> ;
    pav:createdBy <http://orcid.org/0000-0003-0169-8159> ;
    pav:version "v3.0.0.0" .
  dgn-void:disgenetv3.0rdf pav:version "v3.0.0" .
}