@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP563597.RABOxbuIKavXNhl64LwT33PFEV0YkVe06BUC7xgBR3vM4> .
@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:NP563597.RABOxbuIKavXNhl64LwT33PFEV0YkVe06BUC7xgBR3vM4130_head {
  this: np:hasAssertion dgn-np:NP563597.RABOxbuIKavXNhl64LwT33PFEV0YkVe06BUC7xgBR3vM4130_assertion ;
    np:hasProvenance dgn-np:NP563597.RABOxbuIKavXNhl64LwT33PFEV0YkVe06BUC7xgBR3vM4130_provenance ;
    np:hasPublicationInfo dgn-np:NP563597.RABOxbuIKavXNhl64LwT33PFEV0YkVe06BUC7xgBR3vM4130_publicationInfo ;
    a np:Nanopublication .
  dgn-np:NP563597.RABOxbuIKavXNhl64LwT33PFEV0YkVe06BUC7xgBR3vM4130_assertion a np:Assertion .
  dgn-np:NP563597.RABOxbuIKavXNhl64LwT33PFEV0YkVe06BUC7xgBR3vM4130_provenance a np:Provenance .
  dgn-np:NP563597.RABOxbuIKavXNhl64LwT33PFEV0YkVe06BUC7xgBR3vM4130_publicationInfo a np:PublicationInfo .
}
dgn-np:NP563597.RABOxbuIKavXNhl64LwT33PFEV0YkVe06BUC7xgBR3vM4130_assertion {
  miriam-gene:7157 a ncit:C16612 .
  lld:C0280785 a ncit:C7057 .
  dgn-gda:DGN5f707cb8c1219274f96273335e1092fb sio:SIO_000628 miriam-gene:7157 , lld:C0280785 ;
    a sio:SIO_001121 .
}
dgn-np:NP563597.RABOxbuIKavXNhl64LwT33PFEV0YkVe06BUC7xgBR3vM4130_provenance {
  dgn-np:NP563597.RABOxbuIKavXNhl64LwT33PFEV0YkVe06BUC7xgBR3vM4130_assertion dcterms:description "[We had previously reported that loss of heterozygosity (LOH) of the D17S379 locus on 17p13.3 was significantly more frequent in high-grade gliomas (anaplastic astrocytoma, AA; glioblastoma multiforme, GBM) than in those of a low-grade diffuse astrocytoma (DA); however, this was independent of alterations at the TP53 locus, We also showed that LOH of D17S379 was associated with positive staining for p53 protein on immunohistochemistry, but LOH of the TP53 gene had no such association.]. 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:12850379 ;
    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:NP563597.RABOxbuIKavXNhl64LwT33PFEV0YkVe06BUC7xgBR3vM4130_publicationInfo {
  this: dcterms:created "2014-10-02T12:37:39+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> ;
    pav:createdBy <http://orcid.org/0000-0003-0169-8159> ;
    pav:version "v2.1.0.0" .
  dgn-void:disgenetrdf pav:version "v2.1.0" .
}