@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP355496.RABhFkpX5q0EAA5MSXHlt77zEL62i2-dmoHvOqrnBXLdA> .
@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/eco.owl#> .
@prefix wi: <http://purl.org/ontology/wi/core#> .
@prefix prov: <http://www.w3.org/ns/prov#> .
@prefix pav: <http://purl.org/pav/2.0/> .
@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/nanopublications.trig#> .
@prefix dgn-gda: <http://rdf.disgenet.org/gene-disease-association.ttl#> .
@prefix dgn-void: <http://rdf.disgenet.org/v2.1.0/void.ttl#> .

dgn-np:NP355496.RABhFkpX5q0EAA5MSXHlt77zEL62i2-dmoHvOqrnBXLdA130_head {
  this: np:hasAssertion dgn-np:NP355496.RABhFkpX5q0EAA5MSXHlt77zEL62i2-dmoHvOqrnBXLdA130_assertion;
    np:hasProvenance dgn-np:NP355496.RABhFkpX5q0EAA5MSXHlt77zEL62i2-dmoHvOqrnBXLdA130_provenance;
    np:hasPublicationInfo dgn-np:NP355496.RABhFkpX5q0EAA5MSXHlt77zEL62i2-dmoHvOqrnBXLdA130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP355496.RABhFkpX5q0EAA5MSXHlt77zEL62i2-dmoHvOqrnBXLdA130_assertion a np:Assertion .
  
  dgn-np:NP355496.RABhFkpX5q0EAA5MSXHlt77zEL62i2-dmoHvOqrnBXLdA130_provenance a np:Provenance .
  
  dgn-np:NP355496.RABhFkpX5q0EAA5MSXHlt77zEL62i2-dmoHvOqrnBXLdA130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP355496.RABhFkpX5q0EAA5MSXHlt77zEL62i2-dmoHvOqrnBXLdA130_assertion {
  miriam-gene:3757 a ncit:C16612 .
  
  lld:C0018790 a ncit:C7057 .
  
  dgn-gda:DGNd6c596367ea8141a03c78ac99fded1cd sio:SIO_000628 miriam-gene:3757, lld:C0018790;
    a sio:SIO_001121 .
}

dgn-np:NP355496.RABhFkpX5q0EAA5MSXHlt77zEL62i2-dmoHvOqrnBXLdA130_provenance {
  dgn-np:NP355496.RABhFkpX5q0EAA5MSXHlt77zEL62i2-dmoHvOqrnBXLdA130_assertion dcterms:description
      "[In 118 genetically-confirmed LQT2 patients (69 families, 62 KCNH2 mutations), the ECG parameters, Schwartz scores, and the incidence of cardiac events, defined as syncope, aborted cardiac arrest, and sudden cardiac death, were evaluated.]. 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:18441445;
    prov:wasDerivedFrom dgn-void:befree-20140225;
    prov:wasGeneratedBy eco:ECO_0000203 .
  
  dgn-void:befree-20140225 pav:importedOn "2014-02-25"^^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:NP355496.RABhFkpX5q0EAA5MSXHlt77zEL62i2-dmoHvOqrnBXLdA130_publicationInfo {
  this: dcterms:created "2014-10-02T12:35:28+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:disgenetrdf;
    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 "v2.1.0.0" .
  
  dgn-void:disgenetrdf pav:version "v2.1.0" .
}