@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP53607.RAX1_HEXMR9sIkWSto4QXqjOYciBMKGM6-jXp_PRW5mMk> .
@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:NP53607.RAX1_HEXMR9sIkWSto4QXqjOYciBMKGM6-jXp_PRW5mMk130_head {
  this: np:hasAssertion dgn-np:NP53607.RAX1_HEXMR9sIkWSto4QXqjOYciBMKGM6-jXp_PRW5mMk130_assertion;
    np:hasProvenance dgn-np:NP53607.RAX1_HEXMR9sIkWSto4QXqjOYciBMKGM6-jXp_PRW5mMk130_provenance;
    np:hasPublicationInfo dgn-np:NP53607.RAX1_HEXMR9sIkWSto4QXqjOYciBMKGM6-jXp_PRW5mMk130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP53607.RAX1_HEXMR9sIkWSto4QXqjOYciBMKGM6-jXp_PRW5mMk130_assertion a np:Assertion .
  
  dgn-np:NP53607.RAX1_HEXMR9sIkWSto4QXqjOYciBMKGM6-jXp_PRW5mMk130_provenance a np:Provenance .
  
  dgn-np:NP53607.RAX1_HEXMR9sIkWSto4QXqjOYciBMKGM6-jXp_PRW5mMk130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP53607.RAX1_HEXMR9sIkWSto4QXqjOYciBMKGM6-jXp_PRW5mMk130_assertion {
  miriam-gene:4929 a ncit:C16612 .
  
  lld:C0036341 a ncit:C7057 .
  
  dgn-gda:DGN613db1cb18025b5577b2b2eb7534a7c3 sio:SIO_000628 miriam-gene:4929, lld:C0036341;
    a sio:SIO_001122 .
}

dgn-np:NP53607.RAX1_HEXMR9sIkWSto4QXqjOYciBMKGM6-jXp_PRW5mMk130_provenance {
  dgn-np:NP53607.RAX1_HEXMR9sIkWSto4QXqjOYciBMKGM6-jXp_PRW5mMk130_assertion dcterms:description
      "[The study failed to identify any of the described mutations in patients or controls. Nevertheless, these negative results do not exclude altered expression of nuclear receptors in schizophrenia or the presence of other mutations.]. 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:15211629;
    prov:wasDerivedFrom dgn-void:gad-20130706;
    prov:wasGeneratedBy eco:ECO_0000203 .
  
  dgn-void:gad-20130706 pav:importedOn "2013-07-06"^^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:NP53607.RAX1_HEXMR9sIkWSto4QXqjOYciBMKGM6-jXp_PRW5mMk130_publicationInfo {
  this: dcterms:created "2014-10-02T12:32:25+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" .
}