@prefix semsc: <http://semanticscience.org/resource/> .
@prefix dct: <http://purl.org/dc/terms/> .
@prefix orcid: <http://orcid.org/> .
@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP207310.RADfcJCiC1_JVb48GhVDqlTviJ7rrsqq65_r9s_Fgv_14> .
@prefix rdfs: <http://www.w3.org/2000/01/rdf-schema#> .
@prefix xsd: <http://www.w3.org/2001/XMLSchema#> .
@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 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:NP207310.RADfcJCiC1_JVb48GhVDqlTviJ7rrsqq65_r9s_Fgv_14130_head {
  this: np:hasAssertion dgn-np:NP207310.RADfcJCiC1_JVb48GhVDqlTviJ7rrsqq65_r9s_Fgv_14130_assertion;
    np:hasProvenance dgn-np:NP207310.RADfcJCiC1_JVb48GhVDqlTviJ7rrsqq65_r9s_Fgv_14130_provenance;
    np:hasPublicationInfo dgn-np:NP207310.RADfcJCiC1_JVb48GhVDqlTviJ7rrsqq65_r9s_Fgv_14130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP207310.RADfcJCiC1_JVb48GhVDqlTviJ7rrsqq65_r9s_Fgv_14130_assertion a np:Assertion .
  
  dgn-np:NP207310.RADfcJCiC1_JVb48GhVDqlTviJ7rrsqq65_r9s_Fgv_14130_provenance a np:Provenance .
  
  dgn-np:NP207310.RADfcJCiC1_JVb48GhVDqlTviJ7rrsqq65_r9s_Fgv_14130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP207310.RADfcJCiC1_JVb48GhVDqlTviJ7rrsqq65_r9s_Fgv_14130_assertion {
  miriam-gene:91752 a ncit:C16612 .
  
  lld:C0036341 a ncit:C7057 .
  
  dgn-gda:DGN0f723557588e1d583221557c2a14a844 semsc:SIO_000628 miriam-gene:91752, lld:C0036341;
    a semsc:SIO_001121 .
}

dgn-np:NP207310.RADfcJCiC1_JVb48GhVDqlTviJ7rrsqq65_r9s_Fgv_14130_provenance {
  dgn-np:NP207310.RADfcJCiC1_JVb48GhVDqlTviJ7rrsqq65_r9s_Fgv_14130_assertion dct:description
      "[The allelic association at the ZNF804A locus is now one of the most compelling in schizophrenia to date, and supports the accumulating data suggesting overlapping genetic risk between schizophrenia and bipolar disorder.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine."@en;
    wi:evidence dgn-void:source_evidence_literature;
    semsc:SIO_000772 miriam-pubmed:20368704;
    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:NP207310.RADfcJCiC1_JVb48GhVDqlTviJ7rrsqq65_r9s_Fgv_14130_publicationInfo {
  this: dct:created "2014-10-02T12:33:54+02:00"^^xsd:dateTime;
    dct:rights <http://opendatacommons.org/licenses/odbl/1.0/>;
    dct:rightsHolder dgn-void:IBIGroup;
    dct:subject semsc:SIO_000983;
    prv:usedData dgn-void:disgenetrdf;
    pav:authoredBy orcid:0000-0001-5999-6269, orcid:0000-0002-7534-7661, orcid:0000-0002-9383-528X,
      orcid:0000-0003-0169-8159, orcid:0000-0003-1244-7654;
    pav:createdBy orcid:0000-0003-0169-8159;
    pav:version "v2.1.0.0" .
  
  dgn-void:disgenetrdf pav:version "v2.1.0" .
}