@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP407335.RA4wnhg_gVJbhsbAg-kyrfUn7LHQg59JqOzx96q0eFN-k> .
@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:NP407335.RA4wnhg_gVJbhsbAg-kyrfUn7LHQg59JqOzx96q0eFN-k130_head {
  this: np:hasAssertion dgn-np:NP407335.RA4wnhg_gVJbhsbAg-kyrfUn7LHQg59JqOzx96q0eFN-k130_assertion;
    np:hasProvenance dgn-np:NP407335.RA4wnhg_gVJbhsbAg-kyrfUn7LHQg59JqOzx96q0eFN-k130_provenance;
    np:hasPublicationInfo dgn-np:NP407335.RA4wnhg_gVJbhsbAg-kyrfUn7LHQg59JqOzx96q0eFN-k130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP407335.RA4wnhg_gVJbhsbAg-kyrfUn7LHQg59JqOzx96q0eFN-k130_assertion a np:Assertion .
  
  dgn-np:NP407335.RA4wnhg_gVJbhsbAg-kyrfUn7LHQg59JqOzx96q0eFN-k130_provenance a np:Provenance .
  
  dgn-np:NP407335.RA4wnhg_gVJbhsbAg-kyrfUn7LHQg59JqOzx96q0eFN-k130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP407335.RA4wnhg_gVJbhsbAg-kyrfUn7LHQg59JqOzx96q0eFN-k130_assertion {
  miriam-gene:7157 a ncit:C16612 .
  
  lld:C1368871 a ncit:C7057 .
  
  dgn-gda:DGNec954a15bfad9b079d117644b810dac0 sio:SIO_000628 miriam-gene:7157, lld:C1368871;
    a sio:SIO_001121 .
}

dgn-np:NP407335.RA4wnhg_gVJbhsbAg-kyrfUn7LHQg59JqOzx96q0eFN-k130_provenance {
  dgn-np:NP407335.RA4wnhg_gVJbhsbAg-kyrfUn7LHQg59JqOzx96q0eFN-k130_assertion dcterms:description
      "[The colocalization of the p53 tumor suppressor gene to 17p13 raises the possibility that its mutant alleles may play a role in the malignant transformation of `medulloblasts.` Mutations and deletions of the p53 gene have been described in many tumor types and in the germline of some individuals with the Li-Fraumeni syndrome, but reports on the status of the p53 and mdm2 (a gene coding for a p53-associated protein reportedly amplified in human sarcomas) genes in medulloblastomas are few and an indication of their roles, if any, in the etiology of this important childhood tumor has yet to emerge.]. 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:7923211;
    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:NP407335.RA4wnhg_gVJbhsbAg-kyrfUn7LHQg59JqOzx96q0eFN-k130_publicationInfo {
  this: dcterms:created "2014-10-02T12:36:02+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" .
}