@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP426061.RAF26hTFOupqGI0VX16NTXeM2FFOpZOSrie3Ds89-tKQM> .
@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:NP426061.RAF26hTFOupqGI0VX16NTXeM2FFOpZOSrie3Ds89-tKQM130_head {
  this: np:hasAssertion dgn-np:NP426061.RAF26hTFOupqGI0VX16NTXeM2FFOpZOSrie3Ds89-tKQM130_assertion;
    np:hasProvenance dgn-np:NP426061.RAF26hTFOupqGI0VX16NTXeM2FFOpZOSrie3Ds89-tKQM130_provenance;
    np:hasPublicationInfo dgn-np:NP426061.RAF26hTFOupqGI0VX16NTXeM2FFOpZOSrie3Ds89-tKQM130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP426061.RAF26hTFOupqGI0VX16NTXeM2FFOpZOSrie3Ds89-tKQM130_assertion a np:Assertion .
  
  dgn-np:NP426061.RAF26hTFOupqGI0VX16NTXeM2FFOpZOSrie3Ds89-tKQM130_provenance a np:Provenance .
  
  dgn-np:NP426061.RAF26hTFOupqGI0VX16NTXeM2FFOpZOSrie3Ds89-tKQM130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP426061.RAF26hTFOupqGI0VX16NTXeM2FFOpZOSrie3Ds89-tKQM130_assertion {
  miriam-gene:23627 a ncit:C16612 .
  
  lld:C0004114 a ncit:C7057 .
  
  dgn-gda:DGN7787e0c444b622f93977b6a9bf8c028c sio:SIO_000628 miriam-gene:23627, lld:C0004114;
    a sio:SIO_001121 .
}

dgn-np:NP426061.RAF26hTFOupqGI0VX16NTXeM2FFOpZOSrie3Ds89-tKQM130_provenance {
  dgn-np:NP426061.RAF26hTFOupqGI0VX16NTXeM2FFOpZOSrie3Ds89-tKQM130_assertion dcterms:description
      "[Extensive differences in PRND gene expression were also found within each grade of malignancy, suggesting that PRND mRNA quantitation might be useful to distinguish astrocytoma subtypes, and important in disease stratification and in the assessment of specific treatment strategies.]. 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:17390034;
    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:NP426061.RAF26hTFOupqGI0VX16NTXeM2FFOpZOSrie3Ds89-tKQM130_publicationInfo {
  this: dcterms:created "2014-10-02T12:36:12+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" .
}