@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP176119.RA4p7lsFpT5vi0S10sUjnFPdmR2rxDwSU5oPnxSmjNmXk> .
@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:NP176119.RA4p7lsFpT5vi0S10sUjnFPdmR2rxDwSU5oPnxSmjNmXk130_head {
  this: np:hasAssertion dgn-np:NP176119.RA4p7lsFpT5vi0S10sUjnFPdmR2rxDwSU5oPnxSmjNmXk130_assertion ;
    np:hasProvenance dgn-np:NP176119.RA4p7lsFpT5vi0S10sUjnFPdmR2rxDwSU5oPnxSmjNmXk130_provenance ;
    np:hasPublicationInfo dgn-np:NP176119.RA4p7lsFpT5vi0S10sUjnFPdmR2rxDwSU5oPnxSmjNmXk130_publicationInfo ;
    a np:Nanopublication .
  dgn-np:NP176119.RA4p7lsFpT5vi0S10sUjnFPdmR2rxDwSU5oPnxSmjNmXk130_assertion a np:Assertion .
  dgn-np:NP176119.RA4p7lsFpT5vi0S10sUjnFPdmR2rxDwSU5oPnxSmjNmXk130_provenance a np:Provenance .
  dgn-np:NP176119.RA4p7lsFpT5vi0S10sUjnFPdmR2rxDwSU5oPnxSmjNmXk130_publicationInfo a np:PublicationInfo .
}
dgn-np:NP176119.RA4p7lsFpT5vi0S10sUjnFPdmR2rxDwSU5oPnxSmjNmXk130_assertion {
  miriam-gene:7157 a ncit:C16612 .
  lld:C0178874 a ncit:C7057 .
  dgn-gda:DGN483834329b01fe2d8633b7cfa5932b2c sio:SIO_000628 miriam-gene:7157 , lld:C0178874 ;
    a sio:SIO_001121 .
}
dgn-np:NP176119.RA4p7lsFpT5vi0S10sUjnFPdmR2rxDwSU5oPnxSmjNmXk130_provenance {
  dgn-np:NP176119.RA4p7lsFpT5vi0S10sUjnFPdmR2rxDwSU5oPnxSmjNmXk130_assertion dcterms:description "[When compared with the histological grading, the rates of OS for Tel 17p and p53 in anaplastic astrocytomas were higher than those of glioblastomas, suggesting that the deletion may be associated with the early events in tumorigenesis and that some glioblastomas without chromosome 17 aberrations may be independent from tumour progression via low-grade gliomas.]. 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:7865231 ;
    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:NP176119.RA4p7lsFpT5vi0S10sUjnFPdmR2rxDwSU5oPnxSmjNmXk130_publicationInfo {
  this: dcterms:created "2014-10-02T12:33:35+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" .
}