@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP716192.RAl0G0AbXA4TqjV90ExfssFmrsHmT4fNgXvBZT_-lBl2w> .
@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:NP716192.RAl0G0AbXA4TqjV90ExfssFmrsHmT4fNgXvBZT_-lBl2w130_head {
  this: np:hasAssertion dgn-np:NP716192.RAl0G0AbXA4TqjV90ExfssFmrsHmT4fNgXvBZT_-lBl2w130_assertion;
    np:hasProvenance dgn-np:NP716192.RAl0G0AbXA4TqjV90ExfssFmrsHmT4fNgXvBZT_-lBl2w130_provenance;
    np:hasPublicationInfo dgn-np:NP716192.RAl0G0AbXA4TqjV90ExfssFmrsHmT4fNgXvBZT_-lBl2w130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP716192.RAl0G0AbXA4TqjV90ExfssFmrsHmT4fNgXvBZT_-lBl2w130_assertion a np:Assertion .
  
  dgn-np:NP716192.RAl0G0AbXA4TqjV90ExfssFmrsHmT4fNgXvBZT_-lBl2w130_provenance a np:Provenance .
  
  dgn-np:NP716192.RAl0G0AbXA4TqjV90ExfssFmrsHmT4fNgXvBZT_-lBl2w130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP716192.RAl0G0AbXA4TqjV90ExfssFmrsHmT4fNgXvBZT_-lBl2w130_assertion {
  miriam-gene:1810 a ncit:C16612 .
  
  lld:C0036341 a ncit:C7057 .
  
  dgn-gda:DGN84527bb13ac22424ed3fa47232085a67 sio:SIO_000628 miriam-gene:1810, lld:C0036341;
    a sio:SIO_001121 .
}

dgn-np:NP716192.RAl0G0AbXA4TqjV90ExfssFmrsHmT4fNgXvBZT_-lBl2w130_provenance {
  dgn-np:NP716192.RAl0G0AbXA4TqjV90ExfssFmrsHmT4fNgXvBZT_-lBl2w130_assertion dcterms:description
      "[The main focus of this review has been to discuss the probable causes of the higher frequency of HLA DR1 antigen in patients with schizophrenia from Japan and Turkey, and also to see whether there was an impact of belonging to the Ural-Altaic language group.]. 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:16412545;
    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:NP716192.RAl0G0AbXA4TqjV90ExfssFmrsHmT4fNgXvBZT_-lBl2w130_publicationInfo {
  this: dcterms:created "2014-10-02T12:39:15+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" .
}