@prefix this: <http://rdf.disgenet.org/resource/nanopub/NP762496.RAd1BHz6FQElQdWL1mRB8AoiiBqP5p3MkO971b4949nvs> .
@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/v4.0.0/void/> .

dgn-np:NP762496.RAd1BHz6FQElQdWL1mRB8AoiiBqP5p3MkO971b4949nvs130_head {
  this: np:hasAssertion dgn-np:NP762496.RAd1BHz6FQElQdWL1mRB8AoiiBqP5p3MkO971b4949nvs130_assertion;
    np:hasProvenance dgn-np:NP762496.RAd1BHz6FQElQdWL1mRB8AoiiBqP5p3MkO971b4949nvs130_provenance;
    np:hasPublicationInfo dgn-np:NP762496.RAd1BHz6FQElQdWL1mRB8AoiiBqP5p3MkO971b4949nvs130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP762496.RAd1BHz6FQElQdWL1mRB8AoiiBqP5p3MkO971b4949nvs130_assertion a np:Assertion .
  
  dgn-np:NP762496.RAd1BHz6FQElQdWL1mRB8AoiiBqP5p3MkO971b4949nvs130_provenance a np:Provenance .
  
  dgn-np:NP762496.RAd1BHz6FQElQdWL1mRB8AoiiBqP5p3MkO971b4949nvs130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP762496.RAd1BHz6FQElQdWL1mRB8AoiiBqP5p3MkO971b4949nvs130_assertion {
  miriam-gene:6331 a ncit:C16612 .
  
  lld:C0232197 a ncit:C7057 .
  
  dgn-gda:DGN37f7cb65c5623422765ec47af10e84f1 sio:SIO_000628 miriam-gene:6331, lld:C0232197;
    a sio:SIO_001121 .
}

dgn-np:NP762496.RAd1BHz6FQElQdWL1mRB8AoiiBqP5p3MkO971b4949nvs130_provenance {
  dgn-np:NP762496.RAd1BHz6FQElQdWL1mRB8AoiiBqP5p3MkO971b4949nvs130_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-2016;
    prov:wasGeneratedBy eco:ECO_0000203 .
  
  dgn-void:befree-2016 pav:importedOn "2016-02-19"^^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:NP762496.RAd1BHz6FQElQdWL1mRB8AoiiBqP5p3MkO971b4949nvs130_publicationInfo {
  this: dcterms:created "2016-05-13T12:47:30+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 "v4.0.0.0" .
  
  dgn-void:disgenetv3.0rdf pav:version "v4.0.0" .
}