@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP568428.RABAII7iN_va_Nr5m3LAADeRPL65dnC_RfK01CHfHAtfQ> .
@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:NP568428.RABAII7iN_va_Nr5m3LAADeRPL65dnC_RfK01CHfHAtfQ130_head {
  this: np:hasAssertion dgn-np:NP568428.RABAII7iN_va_Nr5m3LAADeRPL65dnC_RfK01CHfHAtfQ130_assertion;
    np:hasProvenance dgn-np:NP568428.RABAII7iN_va_Nr5m3LAADeRPL65dnC_RfK01CHfHAtfQ130_provenance;
    np:hasPublicationInfo dgn-np:NP568428.RABAII7iN_va_Nr5m3LAADeRPL65dnC_RfK01CHfHAtfQ130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP568428.RABAII7iN_va_Nr5m3LAADeRPL65dnC_RfK01CHfHAtfQ130_assertion a np:Assertion .
  
  dgn-np:NP568428.RABAII7iN_va_Nr5m3LAADeRPL65dnC_RfK01CHfHAtfQ130_provenance a np:Provenance .
  
  dgn-np:NP568428.RABAII7iN_va_Nr5m3LAADeRPL65dnC_RfK01CHfHAtfQ130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP568428.RABAII7iN_va_Nr5m3LAADeRPL65dnC_RfK01CHfHAtfQ130_assertion {
  miriam-gene:3342 a ncit:C16612 .
  
  lld:C0017638 a ncit:C7057 .
  
  dgn-gda:DGN73cbadf95f0d2e24acc2fde99df3337e sio:SIO_000628 miriam-gene:3342, lld:C0017638;
    a sio:SIO_001121 .
}

dgn-np:NP568428.RABAII7iN_va_Nr5m3LAADeRPL65dnC_RfK01CHfHAtfQ130_provenance {
  dgn-np:NP568428.RABAII7iN_va_Nr5m3LAADeRPL65dnC_RfK01CHfHAtfQ130_assertion dcterms:description
      "[We investigated 23 pediatric nonependymal, nonpilocytic gliomas for chromosomal copy number aberrations (CNAs) by comparative genomic hybridization (CGH), mutations of isocitrate dehydrogenase (IDH) genes by direct sequencing, and proliferative activity and expression of O-methylguanine-DNA methyltransferase (MGMT) by immunohistochemistry.]. 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:21099717;
    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:NP568428.RABAII7iN_va_Nr5m3LAADeRPL65dnC_RfK01CHfHAtfQ130_publicationInfo {
  this: dcterms:created "2014-10-02T12:37:43+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" .
}