@prefix this: <http://rdf.disgenet.org/resource/nanopub/NP521619.RAFkC9tfhg0bFu4F-YcepdVAJLUKwrOLicN0GW-OIN0Ec> .
@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:NP521619.RAFkC9tfhg0bFu4F-YcepdVAJLUKwrOLicN0GW-OIN0Ec130_head {
  this: np:hasAssertion dgn-np:NP521619.RAFkC9tfhg0bFu4F-YcepdVAJLUKwrOLicN0GW-OIN0Ec130_assertion;
    np:hasProvenance dgn-np:NP521619.RAFkC9tfhg0bFu4F-YcepdVAJLUKwrOLicN0GW-OIN0Ec130_provenance;
    np:hasPublicationInfo dgn-np:NP521619.RAFkC9tfhg0bFu4F-YcepdVAJLUKwrOLicN0GW-OIN0Ec130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP521619.RAFkC9tfhg0bFu4F-YcepdVAJLUKwrOLicN0GW-OIN0Ec130_assertion a np:Assertion .
  
  dgn-np:NP521619.RAFkC9tfhg0bFu4F-YcepdVAJLUKwrOLicN0GW-OIN0Ec130_provenance a np:Provenance .
  
  dgn-np:NP521619.RAFkC9tfhg0bFu4F-YcepdVAJLUKwrOLicN0GW-OIN0Ec130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP521619.RAFkC9tfhg0bFu4F-YcepdVAJLUKwrOLicN0GW-OIN0Ec130_assertion {
  miriam-gene:3757 a ncit:C16612 .
  
  lld:C1141890 a ncit:C7057 .
  
  dgn-gda:DGNad6c17d0a02e1f0dbb2a9c1c89ea65c7 sio:SIO_000628 miriam-gene:3757, lld:C1141890;
    a sio:SIO_001121 .
}

dgn-np:NP521619.RAFkC9tfhg0bFu4F-YcepdVAJLUKwrOLicN0GW-OIN0Ec130_provenance {
  dgn-np:NP521619.RAFkC9tfhg0bFu4F-YcepdVAJLUKwrOLicN0GW-OIN0Ec130_assertion dcterms:description
      "[Patients with congenital long QT syndrome due to potassium channel mutations (LQT1 and LQT2) may elude diagnosis due to normal electrocardiographic findings at rest, yet remain at risk of sudden death during bradycardia or sympathetic stimulation.]. 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:16275192;
    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:NP521619.RAFkC9tfhg0bFu4F-YcepdVAJLUKwrOLicN0GW-OIN0Ec130_publicationInfo {
  this: dcterms:created "2016-05-13T12:45:41+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" .
}