@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP676209.RApHOazvIjqo-et5nUG-jMU9PUTC5y_cquca2WHKKdAjM> .
@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:NP676209.RApHOazvIjqo-et5nUG-jMU9PUTC5y_cquca2WHKKdAjM130_head {
  this: np:hasAssertion dgn-np:NP676209.RApHOazvIjqo-et5nUG-jMU9PUTC5y_cquca2WHKKdAjM130_assertion;
    np:hasProvenance dgn-np:NP676209.RApHOazvIjqo-et5nUG-jMU9PUTC5y_cquca2WHKKdAjM130_provenance;
    np:hasPublicationInfo dgn-np:NP676209.RApHOazvIjqo-et5nUG-jMU9PUTC5y_cquca2WHKKdAjM130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP676209.RApHOazvIjqo-et5nUG-jMU9PUTC5y_cquca2WHKKdAjM130_assertion a np:Assertion .
  
  dgn-np:NP676209.RApHOazvIjqo-et5nUG-jMU9PUTC5y_cquca2WHKKdAjM130_provenance a np:Provenance .
  
  dgn-np:NP676209.RApHOazvIjqo-et5nUG-jMU9PUTC5y_cquca2WHKKdAjM130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP676209.RApHOazvIjqo-et5nUG-jMU9PUTC5y_cquca2WHKKdAjM130_assertion {
  miriam-gene:5062 a ncit:C16612 .
  
  lld:C0027651 a ncit:C7057 .
  
  dgn-gda:DGN5f579c4783a0be6ddc0c48b8dc671ba0 sio:SIO_000628 miriam-gene:5062, lld:C0027651;
    a sio:SIO_001121 .
}

dgn-np:NP676209.RApHOazvIjqo-et5nUG-jMU9PUTC5y_cquca2WHKKdAjM130_provenance {
  dgn-np:NP676209.RApHOazvIjqo-et5nUG-jMU9PUTC5y_cquca2WHKKdAjM130_assertion dcterms:description
      "[We conclude that in solid pseudopapillary neoplasms the activated Wnt-signaling pathway is disrupted, and that p21 and p27 are contributing to this fact by blocking of the hyperphosphorylation of the Rb protein, thus causing the very low proliferation rate characterizing the solid pseudopapillary neoplasms.]. 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:17632456;
    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:NP676209.RApHOazvIjqo-et5nUG-jMU9PUTC5y_cquca2WHKKdAjM130_publicationInfo {
  this: dcterms:created "2014-10-02T12:38:48+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" .
}