@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP273486.RAD531hhBbVTPIKQ8Q604EOylPI-YgSxOQXo96jVbjGlI> .
@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:NP273486.RAD531hhBbVTPIKQ8Q604EOylPI-YgSxOQXo96jVbjGlI130_head {
   this: np:hasAssertion dgn-np:NP273486.RAD531hhBbVTPIKQ8Q604EOylPI-YgSxOQXo96jVbjGlI130_assertion ;
    np:hasProvenance dgn-np:NP273486.RAD531hhBbVTPIKQ8Q604EOylPI-YgSxOQXo96jVbjGlI130_provenance ;
    np:hasPublicationInfo dgn-np:NP273486.RAD531hhBbVTPIKQ8Q604EOylPI-YgSxOQXo96jVbjGlI130_publicationInfo ;
    a np:Nanopublication .
  dgn-np:NP273486.RAD531hhBbVTPIKQ8Q604EOylPI-YgSxOQXo96jVbjGlI130_assertion a np:Assertion .
  dgn-np:NP273486.RAD531hhBbVTPIKQ8Q604EOylPI-YgSxOQXo96jVbjGlI130_provenance a np:Provenance .
  dgn-np:NP273486.RAD531hhBbVTPIKQ8Q604EOylPI-YgSxOQXo96jVbjGlI130_publicationInfo a np:PublicationInfo .
}
dgn-np:NP273486.RAD531hhBbVTPIKQ8Q604EOylPI-YgSxOQXo96jVbjGlI130_assertion {
   miriam-gene:7157 a ncit:C16612 .
  lld:C0431108 a ncit:C7057 .
  dgn-gda:DGNaead086addbf31fc722f251dd3f7ebfd sio:SIO_000628 miriam-gene:7157 , lld:C0431108 ;
    a sio:SIO_001121 .
}
dgn-np:NP273486.RAD531hhBbVTPIKQ8Q604EOylPI-YgSxOQXo96jVbjGlI130_provenance {
   dgn-np:NP273486.RAD531hhBbVTPIKQ8Q604EOylPI-YgSxOQXo96jVbjGlI130_assertion dcterms:description "[Molecular genetic analysis of loss of heterozygosity (LOH) of 1p, 19q, or 10q, p53 mutation, and MGMT promoter methylation was performed in 44 assessable tumor specimens obtained from 46 patients with recurrent malignant gliomas, including 21 with glioblastoma multiforme, 17 with anaplastic astrocytoma, and eight with anaplastic oligoastrocytoma, which have heterogeneous features and variable histological diagnosis, to assess the correlation with the response to TMZ.]. 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:17721049 ;
    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:NP273486.RAD531hhBbVTPIKQ8Q604EOylPI-YgSxOQXo96jVbjGlI130_publicationInfo {
   this: dcterms:created "2014-10-02T12:34:34+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" .
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}