@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP585467.RAukcMC5058QeZo1YYe3tpJXnFH02EHg0DArXoLR9w8wM> .
@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:NP585467.RAukcMC5058QeZo1YYe3tpJXnFH02EHg0DArXoLR9w8wM130_head {
  this: np:hasAssertion dgn-np:NP585467.RAukcMC5058QeZo1YYe3tpJXnFH02EHg0DArXoLR9w8wM130_assertion;
    np:hasProvenance dgn-np:NP585467.RAukcMC5058QeZo1YYe3tpJXnFH02EHg0DArXoLR9w8wM130_provenance;
    np:hasPublicationInfo dgn-np:NP585467.RAukcMC5058QeZo1YYe3tpJXnFH02EHg0DArXoLR9w8wM130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP585467.RAukcMC5058QeZo1YYe3tpJXnFH02EHg0DArXoLR9w8wM130_assertion a np:Assertion .
  
  dgn-np:NP585467.RAukcMC5058QeZo1YYe3tpJXnFH02EHg0DArXoLR9w8wM130_provenance a np:Provenance .
  
  dgn-np:NP585467.RAukcMC5058QeZo1YYe3tpJXnFH02EHg0DArXoLR9w8wM130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP585467.RAukcMC5058QeZo1YYe3tpJXnFH02EHg0DArXoLR9w8wM130_assertion {
  miriam-gene:3737 a ncit:C16612 .
  
  lld:C0004134 a ncit:C7057 .
  
  dgn-gda:DGNeeb96c40123e8275795e889ddd9de584 sio:SIO_000628 miriam-gene:3737, lld:C0004134;
    a sio:SIO_001121 .
}

dgn-np:NP585467.RAukcMC5058QeZo1YYe3tpJXnFH02EHg0DArXoLR9w8wM130_provenance {
  dgn-np:NP585467.RAukcMC5058QeZo1YYe3tpJXnFH02EHg0DArXoLR9w8wM130_assertion dcterms:description
      "[Disruption of the expression, distribution, and density of these channels through deletion or mutation of the genes encoding these channels, Kcna1 and Kcna2, is associated with neurologic pathologies including epilepsy and ataxia in humans and in rodent models.]. 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:22612818;
    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:NP585467.RAukcMC5058QeZo1YYe3tpJXnFH02EHg0DArXoLR9w8wM130_publicationInfo {
  this: dcterms:created "2014-10-02T12:37:52+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" .
}