@prefix this: <http://rdf.disgenet.org/resource/nanopub/NP519438.RAUdw_hVN-KX146B_69QrXi537Ixgc1HDJqLW-c_g0OS0> .
@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:NP519438.RAUdw_hVN-KX146B_69QrXi537Ixgc1HDJqLW-c_g0OS0130_head {
  this: np:hasAssertion dgn-np:NP519438.RAUdw_hVN-KX146B_69QrXi537Ixgc1HDJqLW-c_g0OS0130_assertion;
    np:hasProvenance dgn-np:NP519438.RAUdw_hVN-KX146B_69QrXi537Ixgc1HDJqLW-c_g0OS0130_provenance;
    np:hasPublicationInfo dgn-np:NP519438.RAUdw_hVN-KX146B_69QrXi537Ixgc1HDJqLW-c_g0OS0130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP519438.RAUdw_hVN-KX146B_69QrXi537Ixgc1HDJqLW-c_g0OS0130_assertion a np:Assertion .
  
  dgn-np:NP519438.RAUdw_hVN-KX146B_69QrXi537Ixgc1HDJqLW-c_g0OS0130_provenance a np:Provenance .
  
  dgn-np:NP519438.RAUdw_hVN-KX146B_69QrXi537Ixgc1HDJqLW-c_g0OS0130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP519438.RAUdw_hVN-KX146B_69QrXi537Ixgc1HDJqLW-c_g0OS0130_assertion {
  miriam-gene:1029 a ncit:C16612 .
  
  lld:C0017638 a ncit:C7057 .
  
  dgn-gda:DGN42bc126794912011db73b12aab485350 sio:SIO_000628 miriam-gene:1029, lld:C0017638;
    a sio:SIO_001121 .
}

dgn-np:NP519438.RAUdw_hVN-KX146B_69QrXi537Ixgc1HDJqLW-c_g0OS0130_provenance {
  dgn-np:NP519438.RAUdw_hVN-KX146B_69QrXi537Ixgc1HDJqLW-c_g0OS0130_assertion dcterms:description
      "[Combined evaluation by single clone and whole chromosome analysis plus 'moving average (MA) approach' enabled us to confirm most of the genetic abnormalities previously identified to be associated with glioma progression, including +1q32, +7, -10, -22q, PTEN and p16 loss, and to disclose new small genomic regions, some correlating with grade malignancy.]. 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:16247447;
    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:NP519438.RAUdw_hVN-KX146B_69QrXi537Ixgc1HDJqLW-c_g0OS0130_publicationInfo {
  this: dcterms:created "2016-05-13T12:45:40+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" .
}