@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP404302.RA5EcLICERPibMS_Umx9FCSpPi9bvoUWJVZjcIvAfG91c> .
@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:NP404302.RA5EcLICERPibMS_Umx9FCSpPi9bvoUWJVZjcIvAfG91c130_head {
  this: np:hasAssertion dgn-np:NP404302.RA5EcLICERPibMS_Umx9FCSpPi9bvoUWJVZjcIvAfG91c130_assertion;
    np:hasProvenance dgn-np:NP404302.RA5EcLICERPibMS_Umx9FCSpPi9bvoUWJVZjcIvAfG91c130_provenance;
    np:hasPublicationInfo dgn-np:NP404302.RA5EcLICERPibMS_Umx9FCSpPi9bvoUWJVZjcIvAfG91c130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP404302.RA5EcLICERPibMS_Umx9FCSpPi9bvoUWJVZjcIvAfG91c130_assertion a np:Assertion .
  
  dgn-np:NP404302.RA5EcLICERPibMS_Umx9FCSpPi9bvoUWJVZjcIvAfG91c130_provenance a np:Provenance .
  
  dgn-np:NP404302.RA5EcLICERPibMS_Umx9FCSpPi9bvoUWJVZjcIvAfG91c130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP404302.RA5EcLICERPibMS_Umx9FCSpPi9bvoUWJVZjcIvAfG91c130_assertion {
  miriam-gene:3757 a ncit:C16612 .
  
  lld:C1859062 a ncit:C7057 .
  
  dgn-gda:DGNa1a283437da918e6db9e013345378455 sio:SIO_000628 miriam-gene:3757, lld:C1859062;
    a sio:SIO_001121 .
}

dgn-np:NP404302.RA5EcLICERPibMS_Umx9FCSpPi9bvoUWJVZjcIvAfG91c130_provenance {
  dgn-np:NP404302.RA5EcLICERPibMS_Umx9FCSpPi9bvoUWJVZjcIvAfG91c130_assertion dcterms:description
      "[Our data suggest that the dynamic response of ventricular repolarization to sympathetic stimulation differs between LQT1, LQT2 and LQT3 syndromes, and may explain why the trigger of cardiac events differs between the genotypes.]. 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:12069453;
    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:NP404302.RA5EcLICERPibMS_Umx9FCSpPi9bvoUWJVZjcIvAfG91c130_publicationInfo {
  this: dcterms:created "2014-10-02T12:36:00+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" .
}