@prefix this: <http://rdf.disgenet.org/resource/nanopub/NP589897.RAgg7UNF7kEXDX70RdZq5xuNq_FWjgTQHbKU_gjQz1Nhw> .
@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:NP589897.RAgg7UNF7kEXDX70RdZq5xuNq_FWjgTQHbKU_gjQz1Nhw130_head {
  this: np:hasAssertion dgn-np:NP589897.RAgg7UNF7kEXDX70RdZq5xuNq_FWjgTQHbKU_gjQz1Nhw130_assertion;
    np:hasProvenance dgn-np:NP589897.RAgg7UNF7kEXDX70RdZq5xuNq_FWjgTQHbKU_gjQz1Nhw130_provenance;
    np:hasPublicationInfo dgn-np:NP589897.RAgg7UNF7kEXDX70RdZq5xuNq_FWjgTQHbKU_gjQz1Nhw130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP589897.RAgg7UNF7kEXDX70RdZq5xuNq_FWjgTQHbKU_gjQz1Nhw130_assertion a np:Assertion .
  
  dgn-np:NP589897.RAgg7UNF7kEXDX70RdZq5xuNq_FWjgTQHbKU_gjQz1Nhw130_provenance a np:Provenance .
  
  dgn-np:NP589897.RAgg7UNF7kEXDX70RdZq5xuNq_FWjgTQHbKU_gjQz1Nhw130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP589897.RAgg7UNF7kEXDX70RdZq5xuNq_FWjgTQHbKU_gjQz1Nhw130_assertion {
  miriam-gene:8892 a ncit:C16612 .
  
  lld:C0005586 a ncit:C7057 .
  
  dgn-gda:DGN027dd6762c43e57a54438dfaa4d19ac6 sio:SIO_000628 miriam-gene:8892, lld:C0005586;
    a sio:SIO_001121 .
}

dgn-np:NP589897.RAgg7UNF7kEXDX70RdZq5xuNq_FWjgTQHbKU_gjQz1Nhw130_provenance {
  dgn-np:NP589897.RAgg7UNF7kEXDX70RdZq5xuNq_FWjgTQHbKU_gjQz1Nhw130_assertion dcterms:description
      "[For unknown reasons, oligodendrocytes appear to be particularly prone to defects in the translation initiation complex (EIF2B) and the convergence of these environmental and genomic signalling pathways on this area might well explain their vulnerability in bipolar disorder.]. 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:17239488;
    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:NP589897.RAgg7UNF7kEXDX70RdZq5xuNq_FWjgTQHbKU_gjQz1Nhw130_publicationInfo {
  this: dcterms:created "2016-05-13T12:46:12+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" .
}