@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP33507.RAob0t6_ZuvUoZGPb8xp_mOcZ66jbrBArIZ5p6DDLFYD4> .
@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:NP33507.RAob0t6_ZuvUoZGPb8xp_mOcZ66jbrBArIZ5p6DDLFYD4130_head {
  this: np:hasAssertion dgn-np:NP33507.RAob0t6_ZuvUoZGPb8xp_mOcZ66jbrBArIZ5p6DDLFYD4130_assertion;
    np:hasProvenance dgn-np:NP33507.RAob0t6_ZuvUoZGPb8xp_mOcZ66jbrBArIZ5p6DDLFYD4130_provenance;
    np:hasPublicationInfo dgn-np:NP33507.RAob0t6_ZuvUoZGPb8xp_mOcZ66jbrBArIZ5p6DDLFYD4130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP33507.RAob0t6_ZuvUoZGPb8xp_mOcZ66jbrBArIZ5p6DDLFYD4130_assertion a np:Assertion .
  
  dgn-np:NP33507.RAob0t6_ZuvUoZGPb8xp_mOcZ66jbrBArIZ5p6DDLFYD4130_provenance a np:Provenance .
  
  dgn-np:NP33507.RAob0t6_ZuvUoZGPb8xp_mOcZ66jbrBArIZ5p6DDLFYD4130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP33507.RAob0t6_ZuvUoZGPb8xp_mOcZ66jbrBArIZ5p6DDLFYD4130_assertion {
  miriam-gene:7416 a ncit:C16612 .
  
  lld:C0014544 a ncit:C7057 .
  
  dgn-gda:DGN4b429b29659c9c5dc294257dcbd1e4ac sio:SIO_000628 miriam-gene:7416, lld:C0014544;
    a sio:SIO_001121 .
}

dgn-np:NP33507.RAob0t6_ZuvUoZGPb8xp_mOcZ66jbrBArIZ5p6DDLFYD4130_provenance {
  dgn-np:NP33507.RAob0t6_ZuvUoZGPb8xp_mOcZ66jbrBArIZ5p6DDLFYD4130_assertion dcterms: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:NP33507.RAob0t6_ZuvUoZGPb8xp_mOcZ66jbrBArIZ5p6DDLFYD4130_publicationInfo {
  this: dcterms:created "2014-10-02T12:32:14+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" .
}