@prefix this: <http://rdf.disgenet.org/resource/nanopub/NP521314.RAy61UHSdPC9Cs7JMoGetwmJ5gtEWjlOMVCyQWu9G4G1s> .
@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/v3.0.0/void/> .

dgn-np:NP521314.RAy61UHSdPC9Cs7JMoGetwmJ5gtEWjlOMVCyQWu9G4G1s130_head {
  this: np:hasAssertion dgn-np:NP521314.RAy61UHSdPC9Cs7JMoGetwmJ5gtEWjlOMVCyQWu9G4G1s130_assertion;
    np:hasProvenance dgn-np:NP521314.RAy61UHSdPC9Cs7JMoGetwmJ5gtEWjlOMVCyQWu9G4G1s130_provenance;
    np:hasPublicationInfo dgn-np:NP521314.RAy61UHSdPC9Cs7JMoGetwmJ5gtEWjlOMVCyQWu9G4G1s130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP521314.RAy61UHSdPC9Cs7JMoGetwmJ5gtEWjlOMVCyQWu9G4G1s130_assertion a np:Assertion .
  
  dgn-np:NP521314.RAy61UHSdPC9Cs7JMoGetwmJ5gtEWjlOMVCyQWu9G4G1s130_provenance a np:Provenance .
  
  dgn-np:NP521314.RAy61UHSdPC9Cs7JMoGetwmJ5gtEWjlOMVCyQWu9G4G1s130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP521314.RAy61UHSdPC9Cs7JMoGetwmJ5gtEWjlOMVCyQWu9G4G1s130_assertion {
  miriam-gene:3736 a ncit:C16612 .
  
  lld:C1720189 a ncit:C7057 .
  
  dgn-gda:DGNe0c2d0cea21cff910cd760ab35ea6622 sio:SIO_000628 miriam-gene:3736, lld:C1720189;
    a sio:SIO_001121 .
}

dgn-np:NP521314.RAy61UHSdPC9Cs7JMoGetwmJ5gtEWjlOMVCyQWu9G4G1s130_provenance {
  dgn-np:NP521314.RAy61UHSdPC9Cs7JMoGetwmJ5gtEWjlOMVCyQWu9G4G1s130_assertion dcterms:description
      "[Taken together, these results show that the different mutations in Kv1.1 affect channel function and indicate that both dominant negative effects and haplotype insufficiency may result in the symptoms of EA.]. 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:9526001;
    prov:wasDerivedFrom dgn-void:befree-20150227;
    prov:wasGeneratedBy eco:ECO_0000203 .
  
  dgn-void:befree-20150227 pav:importedOn "2015-02-27"^^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:NP521314.RAy61UHSdPC9Cs7JMoGetwmJ5gtEWjlOMVCyQWu9G4G1s130_publicationInfo {
  this: dcterms:created "2015-08-25T14:42:48+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 "v3.0.0.0" .
  
  dgn-void:disgenetv3.0rdf pav:version "v3.0.0" .
}