@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP344289.RA_WCGKCHJO13k7XKP3zAb4shCd5J1cD2dJu4gOM31YbA> .
@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:NP344289.RA_WCGKCHJO13k7XKP3zAb4shCd5J1cD2dJu4gOM31YbA130_head {
  this: np:hasAssertion dgn-np:NP344289.RA_WCGKCHJO13k7XKP3zAb4shCd5J1cD2dJu4gOM31YbA130_assertion;
    np:hasProvenance dgn-np:NP344289.RA_WCGKCHJO13k7XKP3zAb4shCd5J1cD2dJu4gOM31YbA130_provenance;
    np:hasPublicationInfo dgn-np:NP344289.RA_WCGKCHJO13k7XKP3zAb4shCd5J1cD2dJu4gOM31YbA130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP344289.RA_WCGKCHJO13k7XKP3zAb4shCd5J1cD2dJu4gOM31YbA130_assertion a np:Assertion .
  
  dgn-np:NP344289.RA_WCGKCHJO13k7XKP3zAb4shCd5J1cD2dJu4gOM31YbA130_provenance a np:Provenance .
  
  dgn-np:NP344289.RA_WCGKCHJO13k7XKP3zAb4shCd5J1cD2dJu4gOM31YbA130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP344289.RA_WCGKCHJO13k7XKP3zAb4shCd5J1cD2dJu4gOM31YbA130_assertion {
  miriam-gene:3084 a ncit:C16612 .
  
  lld:C0001614 a ncit:C7057 .
  
  dgn-gda:DGN20ffeaa1208cbd06bc423d12595222a6 sio:SIO_000628 miriam-gene:3084, lld:C0001614;
    a sio:SIO_001121 .
}

dgn-np:NP344289.RA_WCGKCHJO13k7XKP3zAb4shCd5J1cD2dJu4gOM31YbA130_provenance {
  dgn-np:NP344289.RA_WCGKCHJO13k7XKP3zAb4shCd5J1cD2dJu4gOM31YbA130_assertion dcterms:description
      "[Recently, the gene that encodes neuregulin-1 (NRG1) has been identified as a potential susceptibility gene for schizophrenia, and defects in the expression of erbB3, one of the NRG1 receptors, have been shown to occur in the prefrontal cortex of schizophrenic patients, suggesting that NRG1-erbB signaling is involved in the pathogenesis of schizophrenia.]. 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:15162166;
    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:NP344289.RA_WCGKCHJO13k7XKP3zAb4shCd5J1cD2dJu4gOM31YbA130_publicationInfo {
  this: dcterms:created "2014-10-02T12:35:22+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" .
}