@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP776160.RAwFUS_i6J7B9NnwDHNzBV_nPFpnb9fx6q6zZkG1XhdvQ> .
@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:NP776160.RAwFUS_i6J7B9NnwDHNzBV_nPFpnb9fx6q6zZkG1XhdvQ130_head {
  this: np:hasAssertion dgn-np:NP776160.RAwFUS_i6J7B9NnwDHNzBV_nPFpnb9fx6q6zZkG1XhdvQ130_assertion;
    np:hasProvenance dgn-np:NP776160.RAwFUS_i6J7B9NnwDHNzBV_nPFpnb9fx6q6zZkG1XhdvQ130_provenance;
    np:hasPublicationInfo dgn-np:NP776160.RAwFUS_i6J7B9NnwDHNzBV_nPFpnb9fx6q6zZkG1XhdvQ130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP776160.RAwFUS_i6J7B9NnwDHNzBV_nPFpnb9fx6q6zZkG1XhdvQ130_assertion a np:Assertion .
  
  dgn-np:NP776160.RAwFUS_i6J7B9NnwDHNzBV_nPFpnb9fx6q6zZkG1XhdvQ130_provenance a np:Provenance .
  
  dgn-np:NP776160.RAwFUS_i6J7B9NnwDHNzBV_nPFpnb9fx6q6zZkG1XhdvQ130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP776160.RAwFUS_i6J7B9NnwDHNzBV_nPFpnb9fx6q6zZkG1XhdvQ130_assertion {
  miriam-gene:1956 a ncit:C16612 .
  
  lld:C0259783 a ncit:C7057 .
  
  dgn-gda:DGN03f9eb52406d14915631f7b46fb28c75 sio:SIO_000628 miriam-gene:1956, lld:C0259783;
    a sio:SIO_001121 .
}

dgn-np:NP776160.RAwFUS_i6J7B9NnwDHNzBV_nPFpnb9fx6q6zZkG1XhdvQ130_provenance {
  dgn-np:NP776160.RAwFUS_i6J7B9NnwDHNzBV_nPFpnb9fx6q6zZkG1XhdvQ130_assertion dcterms:description
      "[The data are compiled from 150 astrocytic, oligodendroglial, and mixed gliomas that were assessed for genomic alterations characteristic of these neoplasms, i.e., loss of portions of chromosomes 1p, 9p, 10, 17p, 17q, and 19q, mutations of the p53 tumor suppressor gene, and amplification of the EGF receptor (EGFR) gene.]. 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:8586467;
    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:NP776160.RAwFUS_i6J7B9NnwDHNzBV_nPFpnb9fx6q6zZkG1XhdvQ130_publicationInfo {
  this: dcterms:created "2014-10-02T12:39:50+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" .
}