@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP656652.RAatJFw2mqEqHwuWcwQpCqO_bcF27_ExFMtSMenK40098> .
@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:NP656652.RAatJFw2mqEqHwuWcwQpCqO_bcF27_ExFMtSMenK40098130_head {
  this: np:hasAssertion dgn-np:NP656652.RAatJFw2mqEqHwuWcwQpCqO_bcF27_ExFMtSMenK40098130_assertion;
    np:hasProvenance dgn-np:NP656652.RAatJFw2mqEqHwuWcwQpCqO_bcF27_ExFMtSMenK40098130_provenance;
    np:hasPublicationInfo dgn-np:NP656652.RAatJFw2mqEqHwuWcwQpCqO_bcF27_ExFMtSMenK40098130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP656652.RAatJFw2mqEqHwuWcwQpCqO_bcF27_ExFMtSMenK40098130_assertion a np:Assertion .
  
  dgn-np:NP656652.RAatJFw2mqEqHwuWcwQpCqO_bcF27_ExFMtSMenK40098130_provenance a np:Provenance .
  
  dgn-np:NP656652.RAatJFw2mqEqHwuWcwQpCqO_bcF27_ExFMtSMenK40098130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP656652.RAatJFw2mqEqHwuWcwQpCqO_bcF27_ExFMtSMenK40098130_assertion {
  miriam-gene:259 a ncit:C16612 .
  
  lld:C0085136 a ncit:C7057 .
  
  dgn-gda:DGNe84f8e1665eb9b7cc1e93adc99872ee0 sio:SIO_000628 miriam-gene:259, lld:C0085136;
    a sio:SIO_001121 .
}

dgn-np:NP656652.RAatJFw2mqEqHwuWcwQpCqO_bcF27_ExFMtSMenK40098130_provenance {
  dgn-np:NP656652.RAatJFw2mqEqHwuWcwQpCqO_bcF27_ExFMtSMenK40098130_assertion dcterms:description
      "[These findings suggest that reduction of ITI H2 expression correlates with brain tumor progression and that targeting factors responsible for its loss or restoring the ITI supply exogenously may serve as potential therapeutic strategies for a variety of CNS tumors.]. 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:16452202;
    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:NP656652.RAatJFw2mqEqHwuWcwQpCqO_bcF27_ExFMtSMenK40098130_publicationInfo {
  this: dcterms:created "2014-10-02T12:38:35+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" .
}