@prefix dc: <http://purl.org/dc/terms/> .
@prefix orcid: <http://orcid.org/> .
@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP33512.RAC3oYeLaxsa-STtU5dS0QKOm0sURvnmWo5bNaE4eE7lI> .
@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 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:NP33512.RAC3oYeLaxsa-STtU5dS0QKOm0sURvnmWo5bNaE4eE7lI130_head {
  this: np:hasAssertion dgn-np:NP33512.RAC3oYeLaxsa-STtU5dS0QKOm0sURvnmWo5bNaE4eE7lI130_assertion;
    np:hasProvenance dgn-np:NP33512.RAC3oYeLaxsa-STtU5dS0QKOm0sURvnmWo5bNaE4eE7lI130_provenance;
    np:hasPublicationInfo dgn-np:NP33512.RAC3oYeLaxsa-STtU5dS0QKOm0sURvnmWo5bNaE4eE7lI130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP33512.RAC3oYeLaxsa-STtU5dS0QKOm0sURvnmWo5bNaE4eE7lI130_assertion a np:Assertion .
  
  dgn-np:NP33512.RAC3oYeLaxsa-STtU5dS0QKOm0sURvnmWo5bNaE4eE7lI130_provenance a np:Provenance .
  
  dgn-np:NP33512.RAC3oYeLaxsa-STtU5dS0QKOm0sURvnmWo5bNaE4eE7lI130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP33512.RAC3oYeLaxsa-STtU5dS0QKOm0sURvnmWo5bNaE4eE7lI130_assertion {
  miriam-gene:7417 a ncit:C16612 .
  
  lld:C0014544 a ncit:C7057 .
  
  dgn-gda:DGNb1c1f970d2923b25aa127619e895d108 sio:SIO_000628 miriam-gene:7417, lld:C0014544;
    a sio:SIO_001121 .
}

dgn-np:NP33512.RAC3oYeLaxsa-STtU5dS0QKOm0sURvnmWo5bNaE4eE7lI130_provenance {
  dgn-np:NP33512.RAC3oYeLaxsa-STtU5dS0QKOm0sURvnmWo5bNaE4eE7lI130_assertion dc:description
      "[These findings indicate that the increase of VDAC1 and the decrease of VDAC2 play an important role during the process and provide new molecular evidence in understanding mechanism of refractory epilepsy.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine."@en;
    wi:evidence dgn-void:source_evidence_curated;
    sio:SIO_000772 miriam-pubmed:17893921;
    prov:wasDerivedFrom dgn-void:ctd_human-20130708;
    prov:wasGeneratedBy eco:ECO_0000218 .
  
  dgn-void:ctd_human-20130708 pav:importedOn "2013-07-24"^^xsd:date .
  
  dgn-void:source_evidence_curated a eco:ECO_0000205;
    rdfs:comment "Gene-disease associations manually curated."@en;
    rdfs:label "DisGeNET evidence - CURATED"@en .
}

dgn-np:NP33512.RAC3oYeLaxsa-STtU5dS0QKOm0sURvnmWo5bNaE4eE7lI130_publicationInfo {
  this: dc:created "2014-10-02T12:32:14+02:00"^^xsd:dateTime;
    dc:rights <http://opendatacommons.org/licenses/odbl/1.0/>;
    dc:rightsHolder dgn-void:IBIGroup;
    dc:subject sio:SIO_000983;
    prv:usedData dgn-void:disgenetrdf;
    pav:authoredBy orcid:0000-0001-5999-6269, orcid:0000-0002-7534-7661, orcid:0000-0002-9383-528X,
      orcid:0000-0003-0169-8159, orcid:0000-0003-1244-7654;
    pav:createdBy orcid:0000-0003-0169-8159;
    pav:version "v2.1.0.0" .
  
  dgn-void:disgenetrdf pav:version "v2.1.0" .
}