@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP344177.RADcxGoWfb-_AT1hmo2SdnUgbasAOdALN2mUlo6pvM5Ak> .
@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:NP344177.RADcxGoWfb-_AT1hmo2SdnUgbasAOdALN2mUlo6pvM5Ak130_head {
  this: np:hasAssertion dgn-np:NP344177.RADcxGoWfb-_AT1hmo2SdnUgbasAOdALN2mUlo6pvM5Ak130_assertion;
    np:hasProvenance dgn-np:NP344177.RADcxGoWfb-_AT1hmo2SdnUgbasAOdALN2mUlo6pvM5Ak130_provenance;
    np:hasPublicationInfo dgn-np:NP344177.RADcxGoWfb-_AT1hmo2SdnUgbasAOdALN2mUlo6pvM5Ak130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP344177.RADcxGoWfb-_AT1hmo2SdnUgbasAOdALN2mUlo6pvM5Ak130_assertion a np:Assertion .
  
  dgn-np:NP344177.RADcxGoWfb-_AT1hmo2SdnUgbasAOdALN2mUlo6pvM5Ak130_provenance a np:Provenance .
  
  dgn-np:NP344177.RADcxGoWfb-_AT1hmo2SdnUgbasAOdALN2mUlo6pvM5Ak130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP344177.RADcxGoWfb-_AT1hmo2SdnUgbasAOdALN2mUlo6pvM5Ak130_assertion {
  miriam-gene:9378 a ncit:C16612 .
  
  lld:C1510586 a ncit:C7057 .
  
  dgn-gda:DGNa8562284ab9a293c279f8d4eb89ba83d sio:SIO_000628 miriam-gene:9378, lld:C1510586;
    a sio:SIO_001121 .
}

dgn-np:NP344177.RADcxGoWfb-_AT1hmo2SdnUgbasAOdALN2mUlo6pvM5Ak130_provenance {
  dgn-np:NP344177.RADcxGoWfb-_AT1hmo2SdnUgbasAOdALN2mUlo6pvM5Ak130_assertion dcterms:description
      "[A number of genes that undergo radical changes in expression during this transition include candidates for schizophrenia (SZ), bipolar disorder (BD) and autism spectrum disorders (ASD) that function as transcription factors and chromatin modifiers, such as POU3F2 and ZNF804A, and genes coding for cell adhesion proteins implicated in these conditions including NRXN1 and NLGN1.]. 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:21915259;
    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:NP344177.RADcxGoWfb-_AT1hmo2SdnUgbasAOdALN2mUlo6pvM5Ak130_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" .
}