@prefix this: <http://rdf.disgenet.org/resource/nanopub/NP758576.RA9P_H5NteGyTCqFyMOqLhKpyz-o0YTYSZzrpHK06Ejhg> .
@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/v3.0.0/void/> .

dgn-np:NP758576.RA9P_H5NteGyTCqFyMOqLhKpyz-o0YTYSZzrpHK06Ejhg130_head {
  this: np:hasAssertion dgn-np:NP758576.RA9P_H5NteGyTCqFyMOqLhKpyz-o0YTYSZzrpHK06Ejhg130_assertion;
    np:hasProvenance dgn-np:NP758576.RA9P_H5NteGyTCqFyMOqLhKpyz-o0YTYSZzrpHK06Ejhg130_provenance;
    np:hasPublicationInfo dgn-np:NP758576.RA9P_H5NteGyTCqFyMOqLhKpyz-o0YTYSZzrpHK06Ejhg130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP758576.RA9P_H5NteGyTCqFyMOqLhKpyz-o0YTYSZzrpHK06Ejhg130_assertion a np:Assertion .
  
  dgn-np:NP758576.RA9P_H5NteGyTCqFyMOqLhKpyz-o0YTYSZzrpHK06Ejhg130_provenance a np:Provenance .
  
  dgn-np:NP758576.RA9P_H5NteGyTCqFyMOqLhKpyz-o0YTYSZzrpHK06Ejhg130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP758576.RA9P_H5NteGyTCqFyMOqLhKpyz-o0YTYSZzrpHK06Ejhg130_assertion {
  miriam-gene:7248 a ncit:C16612 .
  
  lld:C0004114 a ncit:C7057 .
  
  dgn-gda:DGN3af518a7e3310cb87a4f84c0fcbb6276 sio:SIO_000628 miriam-gene:7248, lld:C0004114;
    a sio:SIO_001121 .
}

dgn-np:NP758576.RA9P_H5NteGyTCqFyMOqLhKpyz-o0YTYSZzrpHK06Ejhg130_provenance {
  dgn-np:NP758576.RA9P_H5NteGyTCqFyMOqLhKpyz-o0YTYSZzrpHK06Ejhg130_assertion dcterms:description
      "[Our results indicate that deletions of chromosome 14q is a recurrent genetic event in the development of astrocytoma and highlight the subchromosomal regions on this chromosome that are likely to contain putative tumour suppressor genes involved in the oncogenesis of astrocytic tumours.]. 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:12107846;
    prov:wasDerivedFrom dgn-void:befree-20150227;
    prov:wasGeneratedBy eco:ECO_0000203 .
  
  dgn-void:befree-20150227 pav:importedOn "2015-02-27"^^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:NP758576.RA9P_H5NteGyTCqFyMOqLhKpyz-o0YTYSZzrpHK06Ejhg130_publicationInfo {
  this: dcterms:created "2015-08-25T14:45:18+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 "v3.0.0.0" .
  
  dgn-void:disgenetv3.0rdf pav:version "v3.0.0" .
}