@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP592901.RAfqhXxZffj2Mg5gU1W8WBTfWqBSrPSG5Q4SDMLmUnFWA> .
@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:NP592901.RAfqhXxZffj2Mg5gU1W8WBTfWqBSrPSG5Q4SDMLmUnFWA130_head {
  this: np:hasAssertion dgn-np:NP592901.RAfqhXxZffj2Mg5gU1W8WBTfWqBSrPSG5Q4SDMLmUnFWA130_assertion;
    np:hasProvenance dgn-np:NP592901.RAfqhXxZffj2Mg5gU1W8WBTfWqBSrPSG5Q4SDMLmUnFWA130_provenance;
    np:hasPublicationInfo dgn-np:NP592901.RAfqhXxZffj2Mg5gU1W8WBTfWqBSrPSG5Q4SDMLmUnFWA130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP592901.RAfqhXxZffj2Mg5gU1W8WBTfWqBSrPSG5Q4SDMLmUnFWA130_assertion a np:Assertion .
  
  dgn-np:NP592901.RAfqhXxZffj2Mg5gU1W8WBTfWqBSrPSG5Q4SDMLmUnFWA130_provenance a np:Provenance .
  
  dgn-np:NP592901.RAfqhXxZffj2Mg5gU1W8WBTfWqBSrPSG5Q4SDMLmUnFWA130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP592901.RAfqhXxZffj2Mg5gU1W8WBTfWqBSrPSG5Q4SDMLmUnFWA130_assertion {
  miriam-gene:6774 a ncit:C16612 .
  
  lld:C1457883 a ncit:C7057 .
  
  dgn-gda:DGN7432eb603076b851b7b992b752909af9 sio:SIO_000628 miriam-gene:6774, lld:C1457883;
    a sio:SIO_001121 .
}

dgn-np:NP592901.RAfqhXxZffj2Mg5gU1W8WBTfWqBSrPSG5Q4SDMLmUnFWA130_provenance {
  dgn-np:NP592901.RAfqhXxZffj2Mg5gU1W8WBTfWqBSrPSG5Q4SDMLmUnFWA130_assertion dcterms:description
      "[Ectopic co-expression of C/EBPbeta and STAT3 reprograms neural stem cells along the aberrant mesenchymal lineage, whereas elimination of the two factors in glioma cells leads to collapse of the mesenchymal signature and reduces tumour aggressiveness.]. 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:20032975;
    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:NP592901.RAfqhXxZffj2Mg5gU1W8WBTfWqBSrPSG5Q4SDMLmUnFWA130_publicationInfo {
  this: dcterms:created "2014-10-02T12:37:56+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" .
}