@prefix this: <http://rdf.disgenet.org/resource/nanopub/NP400763.RA9NovJct4vtEkbepjVC_ikUlliYCHpVE5ESJ1qJ5P8v8> .
@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/> .
@prefix wi: <http://purl.org/ontology/wi/core#> .
@prefix prov: <http://www.w3.org/ns/prov#> .
@prefix pav: <http://purl.org/pav/> .
@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/resource/nanopub/> .
@prefix dgn-gda: <http://rdf.disgenet.org/resource/gda/> .
@prefix dgn-void: <http://rdf.disgenet.org/v4.0.0/void/> .
dgn-np:NP400763.RA9NovJct4vtEkbepjVC_ikUlliYCHpVE5ESJ1qJ5P8v8130_head {
  this: np:hasAssertion dgn-np:NP400763.RA9NovJct4vtEkbepjVC_ikUlliYCHpVE5ESJ1qJ5P8v8130_assertion ;
    np:hasProvenance dgn-np:NP400763.RA9NovJct4vtEkbepjVC_ikUlliYCHpVE5ESJ1qJ5P8v8130_provenance ;
    np:hasPublicationInfo dgn-np:NP400763.RA9NovJct4vtEkbepjVC_ikUlliYCHpVE5ESJ1qJ5P8v8130_publicationInfo ;
    a np:Nanopublication .
  dgn-np:NP400763.RA9NovJct4vtEkbepjVC_ikUlliYCHpVE5ESJ1qJ5P8v8130_assertion a np:Assertion .
  dgn-np:NP400763.RA9NovJct4vtEkbepjVC_ikUlliYCHpVE5ESJ1qJ5P8v8130_provenance a np:Provenance .
  dgn-np:NP400763.RA9NovJct4vtEkbepjVC_ikUlliYCHpVE5ESJ1qJ5P8v8130_publicationInfo a np:PublicationInfo .
}
dgn-np:NP400763.RA9NovJct4vtEkbepjVC_ikUlliYCHpVE5ESJ1qJ5P8v8130_assertion {
  miriam-gene:5728 a ncit:C16612 .
  lld:C1621958 a ncit:C7057 .
  dgn-gda:DGN13630f9851b2764554cc9ea15dd4da8f sio:SIO_000628 miriam-gene:5728 , lld:C1621958 ;
    a sio:SIO_001121 .
}
dgn-np:NP400763.RA9NovJct4vtEkbepjVC_ikUlliYCHpVE5ESJ1qJ5P8v8130_provenance {
  dgn-np:NP400763.RA9NovJct4vtEkbepjVC_ikUlliYCHpVE5ESJ1qJ5P8v8130_assertion dcterms:description "[According to the preliminary findings of this study, in addition to the EGFR gene, amplification of other genes on chromosome 7 and the deletion of PTEN gene and other cancer-related genes on chromosome 10 appeared important to the development of glioblastoma multiforme and were associated with poor prognosis, whereas the combination of chromosome 1p and 19q deletions seems to be an informative molecular marker for better prognosis.]. 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:12845540 ;
    prov:wasDerivedFrom dgn-void:befree-2016 ;
    prov:wasGeneratedBy eco:ECO_0000203 .
  dgn-void:befree-2016 pav:importedOn "2016-02-19"^^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:NP400763.RA9NovJct4vtEkbepjVC_ikUlliYCHpVE5ESJ1qJ5P8v8130_publicationInfo {
  this: dcterms:created "2016-05-13T12:44:47+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:disgenetv3.0rdf ;
    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 "v4.0.0.0" .
  dgn-void:disgenetv3.0rdf pav:version "v4.0.0" .
}