@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP553292.RAAfHgLCfR3X3AB7IdMGHqoonYIAcDfCobDd5tWW5RkN4> .
@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:NP553292.RAAfHgLCfR3X3AB7IdMGHqoonYIAcDfCobDd5tWW5RkN4130_head {
  this: np:hasAssertion dgn-np:NP553292.RAAfHgLCfR3X3AB7IdMGHqoonYIAcDfCobDd5tWW5RkN4130_assertion;
    np:hasProvenance dgn-np:NP553292.RAAfHgLCfR3X3AB7IdMGHqoonYIAcDfCobDd5tWW5RkN4130_provenance;
    np:hasPublicationInfo dgn-np:NP553292.RAAfHgLCfR3X3AB7IdMGHqoonYIAcDfCobDd5tWW5RkN4130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP553292.RAAfHgLCfR3X3AB7IdMGHqoonYIAcDfCobDd5tWW5RkN4130_assertion a np:Assertion .
  
  dgn-np:NP553292.RAAfHgLCfR3X3AB7IdMGHqoonYIAcDfCobDd5tWW5RkN4130_provenance a np:Provenance .
  
  dgn-np:NP553292.RAAfHgLCfR3X3AB7IdMGHqoonYIAcDfCobDd5tWW5RkN4130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP553292.RAAfHgLCfR3X3AB7IdMGHqoonYIAcDfCobDd5tWW5RkN4130_assertion {
  miriam-gene:5313 a ncit:C16612 .
  
  lld:C0015625 a ncit:C7057 .
  
  dgn-gda:DGNbae714a0181bb0688de8100081e828d8 sio:SIO_000628 miriam-gene:5313, lld:C0015625;
    a sio:SIO_001121 .
}

dgn-np:NP553292.RAAfHgLCfR3X3AB7IdMGHqoonYIAcDfCobDd5tWW5RkN4130_provenance {
  dgn-np:NP553292.RAAfHgLCfR3X3AB7IdMGHqoonYIAcDfCobDd5tWW5RkN4130_assertion dcterms:description
      "[Inhibition of PKR by NPM may be one mechanism by which neoplastic clones evolve in sporadic malignancies and in neoplastic cells arising in the context of the cancer predisposition syndrome, Fanconi anemia.]. 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:12882984;
    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:NP553292.RAAfHgLCfR3X3AB7IdMGHqoonYIAcDfCobDd5tWW5RkN4130_publicationInfo {
  this: dcterms:created "2014-10-02T12:37:33+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" .
}