@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP652956.RAToHTQbJh3G9JT3TofaRodkPJ9hu5KZkns5srczxsuPc> .
@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:NP652956.RAToHTQbJh3G9JT3TofaRodkPJ9hu5KZkns5srczxsuPc130_head {
  this: np:hasAssertion dgn-np:NP652956.RAToHTQbJh3G9JT3TofaRodkPJ9hu5KZkns5srczxsuPc130_assertion;
    np:hasProvenance dgn-np:NP652956.RAToHTQbJh3G9JT3TofaRodkPJ9hu5KZkns5srczxsuPc130_provenance;
    np:hasPublicationInfo dgn-np:NP652956.RAToHTQbJh3G9JT3TofaRodkPJ9hu5KZkns5srczxsuPc130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP652956.RAToHTQbJh3G9JT3TofaRodkPJ9hu5KZkns5srczxsuPc130_assertion a np:Assertion .
  
  dgn-np:NP652956.RAToHTQbJh3G9JT3TofaRodkPJ9hu5KZkns5srczxsuPc130_provenance a np:Provenance .
  
  dgn-np:NP652956.RAToHTQbJh3G9JT3TofaRodkPJ9hu5KZkns5srczxsuPc130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP652956.RAToHTQbJh3G9JT3TofaRodkPJ9hu5KZkns5srczxsuPc130_assertion {
  miriam-gene:3084 a ncit:C16612 .
  
  lld:C0595905 a ncit:C7057 .
  
  dgn-gda:DGN12ecf8c5da87f8bb3f33579c41a47ce4 sio:SIO_000628 miriam-gene:3084, lld:C0595905;
    a sio:SIO_001121 .
}

dgn-np:NP652956.RAToHTQbJh3G9JT3TofaRodkPJ9hu5KZkns5srczxsuPc130_provenance {
  dgn-np:NP652956.RAToHTQbJh3G9JT3TofaRodkPJ9hu5KZkns5srczxsuPc130_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:NP652956.RAToHTQbJh3G9JT3TofaRodkPJ9hu5KZkns5srczxsuPc130_publicationInfo {
  this: dcterms:created "2014-10-02T12:38:33+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" .
}