@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP295616.RAytIkliqYSakA22VsB5FqlruF4P78OGaU8lyOWphRBas> .
@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:NP295616.RAytIkliqYSakA22VsB5FqlruF4P78OGaU8lyOWphRBas130_head {
  this: np:hasAssertion dgn-np:NP295616.RAytIkliqYSakA22VsB5FqlruF4P78OGaU8lyOWphRBas130_assertion;
    np:hasProvenance dgn-np:NP295616.RAytIkliqYSakA22VsB5FqlruF4P78OGaU8lyOWphRBas130_provenance;
    np:hasPublicationInfo dgn-np:NP295616.RAytIkliqYSakA22VsB5FqlruF4P78OGaU8lyOWphRBas130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP295616.RAytIkliqYSakA22VsB5FqlruF4P78OGaU8lyOWphRBas130_assertion a np:Assertion .
  
  dgn-np:NP295616.RAytIkliqYSakA22VsB5FqlruF4P78OGaU8lyOWphRBas130_provenance a np:Provenance .
  
  dgn-np:NP295616.RAytIkliqYSakA22VsB5FqlruF4P78OGaU8lyOWphRBas130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP295616.RAytIkliqYSakA22VsB5FqlruF4P78OGaU8lyOWphRBas130_assertion {
  miriam-gene:4609 a ncit:C16612 .
  
  lld:C0376358 a ncit:C7057 .
  
  dgn-gda:DGNbe437b6308e5a4424daf3ac0f6e1006a sio:SIO_000628 miriam-gene:4609, lld:C0376358;
    a sio:SIO_001121 .
}

dgn-np:NP295616.RAytIkliqYSakA22VsB5FqlruF4P78OGaU8lyOWphRBas130_provenance {
  dgn-np:NP295616.RAytIkliqYSakA22VsB5FqlruF4P78OGaU8lyOWphRBas130_assertion dcterms:description
      "[In both normal and malignant prostate tissues, FOXP3 is both necessary and sufficient to transcriptionally repress cMYC, the most commonly overexpressed oncogene in prostate cancer as well as among the aggregates of other cancers.]. 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:19800578;
    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:NP295616.RAytIkliqYSakA22VsB5FqlruF4P78OGaU8lyOWphRBas130_publicationInfo {
  this: dcterms:created "2014-10-02T12:34:48+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" .
}