@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP508098.RAgvSpf_Ce2g85Rw479yZbxqaJ25wfZt2TtvV3Y4kz2YI> .
@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:NP508098.RAgvSpf_Ce2g85Rw479yZbxqaJ25wfZt2TtvV3Y4kz2YI130_head {
  this: np:hasAssertion dgn-np:NP508098.RAgvSpf_Ce2g85Rw479yZbxqaJ25wfZt2TtvV3Y4kz2YI130_assertion;
    np:hasProvenance dgn-np:NP508098.RAgvSpf_Ce2g85Rw479yZbxqaJ25wfZt2TtvV3Y4kz2YI130_provenance;
    np:hasPublicationInfo dgn-np:NP508098.RAgvSpf_Ce2g85Rw479yZbxqaJ25wfZt2TtvV3Y4kz2YI130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP508098.RAgvSpf_Ce2g85Rw479yZbxqaJ25wfZt2TtvV3Y4kz2YI130_assertion a np:Assertion .
  
  dgn-np:NP508098.RAgvSpf_Ce2g85Rw479yZbxqaJ25wfZt2TtvV3Y4kz2YI130_provenance a np:Provenance .
  
  dgn-np:NP508098.RAgvSpf_Ce2g85Rw479yZbxqaJ25wfZt2TtvV3Y4kz2YI130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP508098.RAgvSpf_Ce2g85Rw479yZbxqaJ25wfZt2TtvV3Y4kz2YI130_assertion {
  miriam-gene:4594 a ncit:C16612 .
  
  lld:C0376358 a ncit:C7057 .
  
  dgn-gda:DGN0ffa4ffdb2153a72551822b4b9215d87 sio:SIO_000628 miriam-gene:4594, lld:C0376358;
    a sio:SIO_001121 .
}

dgn-np:NP508098.RAgvSpf_Ce2g85Rw479yZbxqaJ25wfZt2TtvV3Y4kz2YI130_provenance {
  dgn-np:NP508098.RAgvSpf_Ce2g85Rw479yZbxqaJ25wfZt2TtvV3Y4kz2YI130_assertion dcterms:description
      "[Taken together, our data show that induction of MEK5/ERK5 signalling is linked to activation of the DNA replication licensing pathway in PCa, and that the strong prognostic value of MCM proteins may result from their function as relay stations coupling growth regulatory pathways to genome duplication.]. 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:17406359;
    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:NP508098.RAgvSpf_Ce2g85Rw479yZbxqaJ25wfZt2TtvV3Y4kz2YI130_publicationInfo {
  this: dcterms:created "2014-10-02T12:37:03+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" .
}