@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP850044.RAZyidokCXaQubb6IyRWxujuQ16D-VZZooTR_cCO1yWu8> .
@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:NP850044.RAZyidokCXaQubb6IyRWxujuQ16D-VZZooTR_cCO1yWu8130_head {
  this: np:hasAssertion dgn-np:NP850044.RAZyidokCXaQubb6IyRWxujuQ16D-VZZooTR_cCO1yWu8130_assertion ;
    np:hasProvenance dgn-np:NP850044.RAZyidokCXaQubb6IyRWxujuQ16D-VZZooTR_cCO1yWu8130_provenance ;
    np:hasPublicationInfo dgn-np:NP850044.RAZyidokCXaQubb6IyRWxujuQ16D-VZZooTR_cCO1yWu8130_publicationInfo ;
    a np:Nanopublication .
  dgn-np:NP850044.RAZyidokCXaQubb6IyRWxujuQ16D-VZZooTR_cCO1yWu8130_assertion a np:Assertion .
  dgn-np:NP850044.RAZyidokCXaQubb6IyRWxujuQ16D-VZZooTR_cCO1yWu8130_provenance a np:Provenance .
  dgn-np:NP850044.RAZyidokCXaQubb6IyRWxujuQ16D-VZZooTR_cCO1yWu8130_publicationInfo a np:PublicationInfo .
}
dgn-np:NP850044.RAZyidokCXaQubb6IyRWxujuQ16D-VZZooTR_cCO1yWu8130_assertion {
  miriam-gene:1956 a ncit:C16612 .
  lld:C0334583 a ncit:C7057 .
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    a sio:SIO_001121 .
}
dgn-np:NP850044.RAZyidokCXaQubb6IyRWxujuQ16D-VZZooTR_cCO1yWu8130_provenance {
  dgn-np:NP850044.RAZyidokCXaQubb6IyRWxujuQ16D-VZZooTR_cCO1yWu8130_assertion dcterms:description "[To characterize some of the genetic events underlying the development of glioblastoma multiforme, the authors analyzed 65 astrocytic tumors (seven pilocytic astrocytomas, eight astrocytomas, 16 anaplastic astrocytomas, and 34 glioblastomas multiforme) for loss of heterozygosity for chromosome 17p, loss of heterozygosity for chromosomes 10p and 10q, amplification of the epidermal growth factor receptor (EGFR) gene, and amplification of the oncogenes N-myc, c-myc, and N-ras using Southern blot analysis.]. 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:8057151 ;
    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:NP850044.RAZyidokCXaQubb6IyRWxujuQ16D-VZZooTR_cCO1yWu8130_publicationInfo {
  this: dcterms:created "2014-10-02T12:40:39+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> ;
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}