@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP523321.RA7GID5_PlJcxp0qxr5AGUO6d93D0gqQdMKviFO-MGSQo> .
@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:NP523321.RA7GID5_PlJcxp0qxr5AGUO6d93D0gqQdMKviFO-MGSQo130_head {
  this: np:hasAssertion dgn-np:NP523321.RA7GID5_PlJcxp0qxr5AGUO6d93D0gqQdMKviFO-MGSQo130_assertion;
    np:hasProvenance dgn-np:NP523321.RA7GID5_PlJcxp0qxr5AGUO6d93D0gqQdMKviFO-MGSQo130_provenance;
    np:hasPublicationInfo dgn-np:NP523321.RA7GID5_PlJcxp0qxr5AGUO6d93D0gqQdMKviFO-MGSQo130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP523321.RA7GID5_PlJcxp0qxr5AGUO6d93D0gqQdMKviFO-MGSQo130_assertion a np:Assertion .
  
  dgn-np:NP523321.RA7GID5_PlJcxp0qxr5AGUO6d93D0gqQdMKviFO-MGSQo130_provenance a np:Provenance .
  
  dgn-np:NP523321.RA7GID5_PlJcxp0qxr5AGUO6d93D0gqQdMKviFO-MGSQo130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP523321.RA7GID5_PlJcxp0qxr5AGUO6d93D0gqQdMKviFO-MGSQo130_assertion {
  miriam-gene:1728 a ncit:C16612 .
  
  lld:C0036341 a ncit:C7057 .
  
  dgn-gda:DGN9e6bde88a544daffdf1996d7db93dcb4 sio:SIO_000628 miriam-gene:1728, lld:C0036341;
    a sio:SIO_001121 .
}

dgn-np:NP523321.RA7GID5_PlJcxp0qxr5AGUO6d93D0gqQdMKviFO-MGSQo130_provenance {
  dgn-np:NP523321.RA7GID5_PlJcxp0qxr5AGUO6d93D0gqQdMKviFO-MGSQo130_assertion dcterms:description
      "[The aim of the present study was to investigate the association between multiple polymorphisms in genes for the central apoptotic protein p53 and its regulator NQO1 and the susceptibility for developing schizophrenia in an Arab population from Syria.]. 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:23360829;
    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:NP523321.RA7GID5_PlJcxp0qxr5AGUO6d93D0gqQdMKviFO-MGSQo130_publicationInfo {
  this: dcterms:created "2014-10-02T12:37:11+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" .
}