@prefix this: <http://rdf.disgenet.org/resource/nanopub/NP263427.RABDB7Re5AJ286goUALkTc-dM3D7F0YavpCwTJg1oQyt0> .
@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:NP263427.RABDB7Re5AJ286goUALkTc-dM3D7F0YavpCwTJg1oQyt0130_head {
  this: np:hasAssertion dgn-np:NP263427.RABDB7Re5AJ286goUALkTc-dM3D7F0YavpCwTJg1oQyt0130_assertion;
    np:hasProvenance dgn-np:NP263427.RABDB7Re5AJ286goUALkTc-dM3D7F0YavpCwTJg1oQyt0130_provenance;
    np:hasPublicationInfo dgn-np:NP263427.RABDB7Re5AJ286goUALkTc-dM3D7F0YavpCwTJg1oQyt0130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP263427.RABDB7Re5AJ286goUALkTc-dM3D7F0YavpCwTJg1oQyt0130_assertion a np:Assertion .
  
  dgn-np:NP263427.RABDB7Re5AJ286goUALkTc-dM3D7F0YavpCwTJg1oQyt0130_provenance a np:Provenance .
  
  dgn-np:NP263427.RABDB7Re5AJ286goUALkTc-dM3D7F0YavpCwTJg1oQyt0130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP263427.RABDB7Re5AJ286goUALkTc-dM3D7F0YavpCwTJg1oQyt0130_assertion {
  miriam-gene:3757 a ncit:C16612 .
  
  lld:C0023976 a ncit:C7057 .
  
  dgn-gda:DGNf216f4f1aa2430e59aebf24370717c3a sio:SIO_000628 miriam-gene:3757, lld:C0023976;
    a sio:SIO_001121 .
}

dgn-np:NP263427.RABDB7Re5AJ286goUALkTc-dM3D7F0YavpCwTJg1oQyt0130_provenance {
  dgn-np:NP263427.RABDB7Re5AJ286goUALkTc-dM3D7F0YavpCwTJg1oQyt0130_assertion dcterms:description
      "[Background-In long-QT syndrome (LQTS), heterozygosity for a mutation in 1 of the K(+) channel genes leads to prolongation of the cardiac action potential, because the aberrant protein exhibits loss of function. HERG, which is involved in LQT2, is the gene encoding the rapid component of the delayed rectifier, I(Kr).]. 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:10491368;
    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:NP263427.RABDB7Re5AJ286goUALkTc-dM3D7F0YavpCwTJg1oQyt0130_publicationInfo {
  this: dcterms:created "2016-05-13T12:43:45+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" .
}