@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP529651.RAOCvFtOP3qjLGcuO5L5uWkg2IfL4i9gNRA5udT_FO9bs> .
@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:NP529651.RAOCvFtOP3qjLGcuO5L5uWkg2IfL4i9gNRA5udT_FO9bs130_head {
  this: np:hasAssertion dgn-np:NP529651.RAOCvFtOP3qjLGcuO5L5uWkg2IfL4i9gNRA5udT_FO9bs130_assertion;
    np:hasProvenance dgn-np:NP529651.RAOCvFtOP3qjLGcuO5L5uWkg2IfL4i9gNRA5udT_FO9bs130_provenance;
    np:hasPublicationInfo dgn-np:NP529651.RAOCvFtOP3qjLGcuO5L5uWkg2IfL4i9gNRA5udT_FO9bs130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP529651.RAOCvFtOP3qjLGcuO5L5uWkg2IfL4i9gNRA5udT_FO9bs130_assertion a np:Assertion .
  
  dgn-np:NP529651.RAOCvFtOP3qjLGcuO5L5uWkg2IfL4i9gNRA5udT_FO9bs130_provenance a np:Provenance .
  
  dgn-np:NP529651.RAOCvFtOP3qjLGcuO5L5uWkg2IfL4i9gNRA5udT_FO9bs130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP529651.RAOCvFtOP3qjLGcuO5L5uWkg2IfL4i9gNRA5udT_FO9bs130_assertion {
  miriam-gene:1523 a ncit:C16612 .
  
  lld:C0023418 a ncit:C7057 .
  
  dgn-gda:DGN8527b815680a16e0f16a36b6773cb28f sio:SIO_000628 miriam-gene:1523, lld:C0023418;
    a sio:SIO_001121 .
}

dgn-np:NP529651.RAOCvFtOP3qjLGcuO5L5uWkg2IfL4i9gNRA5udT_FO9bs130_provenance {
  dgn-np:NP529651.RAOCvFtOP3qjLGcuO5L5uWkg2IfL4i9gNRA5udT_FO9bs130_assertion dcterms:description
      "[Because of the implication of Plzf in the regulation of stem cell maintenance, as well as Wnt and Ras signaling, in other systems, our observations suggest that the novel genetic relationship between CUX1 and PLZF could be of relevance to human diseases, such as leukemia, and open up a new field of investigation for the implication of these regulators during intestinal polyposis and cancer.]. 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:20945532;
    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:NP529651.RAOCvFtOP3qjLGcuO5L5uWkg2IfL4i9gNRA5udT_FO9bs130_publicationInfo {
  this: dcterms:created "2014-10-02T12:37:20+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" .
}