@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP777401.RA_ENeC5GnoOd1xK65JHJN__MH1UEEgZ9HaREFhGvXjGc> .
@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:NP777401.RA_ENeC5GnoOd1xK65JHJN__MH1UEEgZ9HaREFhGvXjGc130_head {
  this: np:hasAssertion dgn-np:NP777401.RA_ENeC5GnoOd1xK65JHJN__MH1UEEgZ9HaREFhGvXjGc130_assertion;
    np:hasProvenance dgn-np:NP777401.RA_ENeC5GnoOd1xK65JHJN__MH1UEEgZ9HaREFhGvXjGc130_provenance;
    np:hasPublicationInfo dgn-np:NP777401.RA_ENeC5GnoOd1xK65JHJN__MH1UEEgZ9HaREFhGvXjGc130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP777401.RA_ENeC5GnoOd1xK65JHJN__MH1UEEgZ9HaREFhGvXjGc130_assertion a np:Assertion .
  
  dgn-np:NP777401.RA_ENeC5GnoOd1xK65JHJN__MH1UEEgZ9HaREFhGvXjGc130_provenance a np:Provenance .
  
  dgn-np:NP777401.RA_ENeC5GnoOd1xK65JHJN__MH1UEEgZ9HaREFhGvXjGc130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP777401.RA_ENeC5GnoOd1xK65JHJN__MH1UEEgZ9HaREFhGvXjGc130_assertion {
  miriam-gene:6584 a ncit:C16612 .
  
  lld:C0040479 a ncit:C7057 .
  
  dgn-gda:DGN561216aa6a27a3ba3923430fc93c1931 sio:SIO_000628 miriam-gene:6584, lld:C0040479;
    a sio:SIO_001121 .
}

dgn-np:NP777401.RA_ENeC5GnoOd1xK65JHJN__MH1UEEgZ9HaREFhGvXjGc130_provenance {
  dgn-np:NP777401.RA_ENeC5GnoOd1xK65JHJN__MH1UEEgZ9HaREFhGvXjGc130_assertion dcterms:description
      "[One of the most important and challenging aspects of caring for patients with congenital long QT syndrome (LQTS) is assessing an individual's risk of sudden cardiac death (SCD) because of torsades de pointes.]. 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:21907997;
    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:NP777401.RA_ENeC5GnoOd1xK65JHJN__MH1UEEgZ9HaREFhGvXjGc130_publicationInfo {
  this: dcterms:created "2014-10-02T12:39:51+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" .
}