@prefix this: <http://rdf.disgenet.org/resource/nanopub/NP644141.RA_-c53rE_mlC5z0hyOaVW0dHl4U-P9ZUGevDaWSaruPs> .
@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:NP644141.RA_-c53rE_mlC5z0hyOaVW0dHl4U-P9ZUGevDaWSaruPs130_head {
  this: np:hasAssertion dgn-np:NP644141.RA_-c53rE_mlC5z0hyOaVW0dHl4U-P9ZUGevDaWSaruPs130_assertion;
    np:hasProvenance dgn-np:NP644141.RA_-c53rE_mlC5z0hyOaVW0dHl4U-P9ZUGevDaWSaruPs130_provenance;
    np:hasPublicationInfo dgn-np:NP644141.RA_-c53rE_mlC5z0hyOaVW0dHl4U-P9ZUGevDaWSaruPs130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP644141.RA_-c53rE_mlC5z0hyOaVW0dHl4U-P9ZUGevDaWSaruPs130_assertion a np:Assertion .
  
  dgn-np:NP644141.RA_-c53rE_mlC5z0hyOaVW0dHl4U-P9ZUGevDaWSaruPs130_provenance a np:Provenance .
  
  dgn-np:NP644141.RA_-c53rE_mlC5z0hyOaVW0dHl4U-P9ZUGevDaWSaruPs130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP644141.RA_-c53rE_mlC5z0hyOaVW0dHl4U-P9ZUGevDaWSaruPs130_assertion {
  miriam-gene:6331 a ncit:C16612 .
  
  lld:C0023976 a ncit:C7057 .
  
  dgn-gda:DGN640d3cf045b3f69c47d41f1d328e169e sio:SIO_000628 miriam-gene:6331, lld:C0023976;
    a sio:SIO_001121 .
}

dgn-np:NP644141.RA_-c53rE_mlC5z0hyOaVW0dHl4U-P9ZUGevDaWSaruPs130_provenance {
  dgn-np:NP644141.RA_-c53rE_mlC5z0hyOaVW0dHl4U-P9ZUGevDaWSaruPs130_assertion dcterms:description
      "[The aim of the present study was to elucidate the molecular mechanism underlying the concomitant occurrence of cardiac conduction disease and long QT syndrome (LQT3), two SCN5A channelopathies that are explained by loss-of-function and gain-of-function, respectively, in the cardiac Na+ channel.]. 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:18065446;
    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:NP644141.RA_-c53rE_mlC5z0hyOaVW0dHl4U-P9ZUGevDaWSaruPs130_publicationInfo {
  this: dcterms:created "2016-05-13T12:46:37+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" .
}