@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP755876.RA-BEivM-InCf-93s7AKJx9h6NtqkGhmEtBxBNMEfKrpU> .
@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:NP755876.RA-BEivM-InCf-93s7AKJx9h6NtqkGhmEtBxBNMEfKrpU130_head {
  this: np:hasAssertion dgn-np:NP755876.RA-BEivM-InCf-93s7AKJx9h6NtqkGhmEtBxBNMEfKrpU130_assertion ;
    np:hasProvenance dgn-np:NP755876.RA-BEivM-InCf-93s7AKJx9h6NtqkGhmEtBxBNMEfKrpU130_provenance ;
    np:hasPublicationInfo dgn-np:NP755876.RA-BEivM-InCf-93s7AKJx9h6NtqkGhmEtBxBNMEfKrpU130_publicationInfo ;
    a np:Nanopublication .
  dgn-np:NP755876.RA-BEivM-InCf-93s7AKJx9h6NtqkGhmEtBxBNMEfKrpU130_assertion a np:Assertion .
  dgn-np:NP755876.RA-BEivM-InCf-93s7AKJx9h6NtqkGhmEtBxBNMEfKrpU130_provenance a np:Provenance .
  dgn-np:NP755876.RA-BEivM-InCf-93s7AKJx9h6NtqkGhmEtBxBNMEfKrpU130_publicationInfo a np:PublicationInfo .
}
dgn-np:NP755876.RA-BEivM-InCf-93s7AKJx9h6NtqkGhmEtBxBNMEfKrpU130_assertion {
  miriam-gene:3815 a ncit:C16612 .
  lld:C0017636 a ncit:C7057 .
  dgn-gda:DGN82df70353987197e76cb44947f0d1089 sio:SIO_000628 miriam-gene:3815 , lld:C0017636 ;
    a sio:SIO_001121 .
}
dgn-np:NP755876.RA-BEivM-InCf-93s7AKJx9h6NtqkGhmEtBxBNMEfKrpU130_provenance {
  dgn-np:NP755876.RA-BEivM-InCf-93s7AKJx9h6NtqkGhmEtBxBNMEfKrpU130_assertion dcterms:description "[No significant difference was observed in the frequency of amplification of these genes in primary and secondary glioblastomas or in glioblastomas with and without IDH1 mutations, suggesting that amplification of PDGFRA, KIT and KDR may be implicated in the pathogenesis of a small fraction of both subtypes of glioblastoma.]. 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:21382095 ;
    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:NP755876.RA-BEivM-InCf-93s7AKJx9h6NtqkGhmEtBxBNMEfKrpU130_publicationInfo {
  this: dcterms:created "2014-10-02T12:39:38+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" .
}