@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP61111.RAVmtwfDKeiRtt_V9lGvn5-111MA7IyGSGAEwm3PeRbC8> .
@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:NP61111.RAVmtwfDKeiRtt_V9lGvn5-111MA7IyGSGAEwm3PeRbC8130_head {
  this: np:hasAssertion dgn-np:NP61111.RAVmtwfDKeiRtt_V9lGvn5-111MA7IyGSGAEwm3PeRbC8130_assertion;
    np:hasProvenance dgn-np:NP61111.RAVmtwfDKeiRtt_V9lGvn5-111MA7IyGSGAEwm3PeRbC8130_provenance;
    np:hasPublicationInfo dgn-np:NP61111.RAVmtwfDKeiRtt_V9lGvn5-111MA7IyGSGAEwm3PeRbC8130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP61111.RAVmtwfDKeiRtt_V9lGvn5-111MA7IyGSGAEwm3PeRbC8130_assertion a np:Assertion .
  
  dgn-np:NP61111.RAVmtwfDKeiRtt_V9lGvn5-111MA7IyGSGAEwm3PeRbC8130_provenance a np:Provenance .
  
  dgn-np:NP61111.RAVmtwfDKeiRtt_V9lGvn5-111MA7IyGSGAEwm3PeRbC8130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP61111.RAVmtwfDKeiRtt_V9lGvn5-111MA7IyGSGAEwm3PeRbC8130_assertion {
  miriam-gene:3784 a ncit:C16612 .
  
  lld:C0023976 a ncit:C7057 .
  
  dgn-gda:DGN12d7819a73bff607ea5f3a910142b026 sio:SIO_000628 miriam-gene:3784, lld:C0023976;
    a sio:SIO_001122 .
}

dgn-np:NP61111.RAVmtwfDKeiRtt_V9lGvn5-111MA7IyGSGAEwm3PeRbC8130_provenance {
  dgn-np:NP61111.RAVmtwfDKeiRtt_V9lGvn5-111MA7IyGSGAEwm3PeRbC8130_assertion dcterms:description
      "[KCNQ1 and KCNH2 are the two most common potassium channel genes causing long QT syndrome (LQTS), an inherited cardiac arrhythmia featured by QT prolongation and increased risks of developing torsade de pointes and sudden death.]. 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:18808722;
    prov:wasDerivedFrom dgn-void:gad-20130706;
    prov:wasGeneratedBy eco:ECO_0000203 .
  
  dgn-void:gad-20130706 pav:importedOn "2013-07-06"^^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:NP61111.RAVmtwfDKeiRtt_V9lGvn5-111MA7IyGSGAEwm3PeRbC8130_publicationInfo {
  this: dcterms:created "2014-10-02T12:32:29+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" .
}