@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP311500.RA2oLLPGynKxqll-lQKTWYtkUn7S1X2oeSyoOLAnXwfVs> .
@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:NP311500.RA2oLLPGynKxqll-lQKTWYtkUn7S1X2oeSyoOLAnXwfVs130_head {
  this: np:hasAssertion dgn-np:NP311500.RA2oLLPGynKxqll-lQKTWYtkUn7S1X2oeSyoOLAnXwfVs130_assertion;
    np:hasProvenance dgn-np:NP311500.RA2oLLPGynKxqll-lQKTWYtkUn7S1X2oeSyoOLAnXwfVs130_provenance;
    np:hasPublicationInfo dgn-np:NP311500.RA2oLLPGynKxqll-lQKTWYtkUn7S1X2oeSyoOLAnXwfVs130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP311500.RA2oLLPGynKxqll-lQKTWYtkUn7S1X2oeSyoOLAnXwfVs130_assertion a np:Assertion .
  
  dgn-np:NP311500.RA2oLLPGynKxqll-lQKTWYtkUn7S1X2oeSyoOLAnXwfVs130_provenance a np:Provenance .
  
  dgn-np:NP311500.RA2oLLPGynKxqll-lQKTWYtkUn7S1X2oeSyoOLAnXwfVs130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP311500.RA2oLLPGynKxqll-lQKTWYtkUn7S1X2oeSyoOLAnXwfVs130_assertion {
  miriam-gene:91752 a ncit:C16612 .
  
  lld:C0349204 a ncit:C7057 .
  
  dgn-gda:DGN805a454dab78df941a17de40c5b3717d sio:SIO_000628 miriam-gene:91752, lld:C0349204;
    a sio:SIO_001121 .
}

dgn-np:NP311500.RA2oLLPGynKxqll-lQKTWYtkUn7S1X2oeSyoOLAnXwfVs130_provenance {
  dgn-np:NP311500.RA2oLLPGynKxqll-lQKTWYtkUn7S1X2oeSyoOLAnXwfVs130_assertion dcterms:description
      "[Genetic imaging studies link the SZ risk variant rs1344706 on the ZNF804A gene to psychosis via alterations in functional brain connectivity during WM, but no work has looked at the effects of ZNF804A on WM with face-processing components.]. 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:23295962;
    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:NP311500.RA2oLLPGynKxqll-lQKTWYtkUn7S1X2oeSyoOLAnXwfVs130_publicationInfo {
  this: dcterms:created "2014-10-02T12:34:58+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" .
}