@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP248591.RAHsdoeDvbEeLoYeb2VaqV7SPigpZ6B852ooM7p0BcUT4> .
@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:NP248591.RAHsdoeDvbEeLoYeb2VaqV7SPigpZ6B852ooM7p0BcUT4130_head {
  this: np:hasAssertion dgn-np:NP248591.RAHsdoeDvbEeLoYeb2VaqV7SPigpZ6B852ooM7p0BcUT4130_assertion;
    np:hasProvenance dgn-np:NP248591.RAHsdoeDvbEeLoYeb2VaqV7SPigpZ6B852ooM7p0BcUT4130_provenance;
    np:hasPublicationInfo dgn-np:NP248591.RAHsdoeDvbEeLoYeb2VaqV7SPigpZ6B852ooM7p0BcUT4130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP248591.RAHsdoeDvbEeLoYeb2VaqV7SPigpZ6B852ooM7p0BcUT4130_assertion a np:Assertion .
  
  dgn-np:NP248591.RAHsdoeDvbEeLoYeb2VaqV7SPigpZ6B852ooM7p0BcUT4130_provenance a np:Provenance .
  
  dgn-np:NP248591.RAHsdoeDvbEeLoYeb2VaqV7SPigpZ6B852ooM7p0BcUT4130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP248591.RAHsdoeDvbEeLoYeb2VaqV7SPigpZ6B852ooM7p0BcUT4130_assertion {
  miriam-gene:4900 a ncit:C16612 .
  
  lld:C0036341 a ncit:C7057 .
  
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    a sio:SIO_001121 .
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dgn-np:NP248591.RAHsdoeDvbEeLoYeb2VaqV7SPigpZ6B852ooM7p0BcUT4130_provenance {
  dgn-np:NP248591.RAHsdoeDvbEeLoYeb2VaqV7SPigpZ6B852ooM7p0BcUT4130_assertion dcterms:description
      "[Our results confirm that common risk factors in the major histocompatibility complex region and TCF4 gene are associated with schizophrenia in Han Chinese, but our results fail to show an association with SNP rs12807809 in the NRGN gene.]. 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:20673877;
    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:NP248591.RAHsdoeDvbEeLoYeb2VaqV7SPigpZ6B852ooM7p0BcUT4130_publicationInfo {
  this: dcterms:created "2014-10-02T12:34:19+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>,
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    pav:createdBy <http://orcid.org/0000-0003-0169-8159>;
    pav:version "v2.1.0.0" .
  
  dgn-void:disgenetrdf pav:version "v2.1.0" .
}