@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP244896.RAdYN4wwDBTwlFbCdWvYXAEwqDT-aeWkJtXxgB_OZ9m1Q> .
@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:NP244896.RAdYN4wwDBTwlFbCdWvYXAEwqDT-aeWkJtXxgB_OZ9m1Q130_head {
  this: np:hasAssertion dgn-np:NP244896.RAdYN4wwDBTwlFbCdWvYXAEwqDT-aeWkJtXxgB_OZ9m1Q130_assertion;
    np:hasProvenance dgn-np:NP244896.RAdYN4wwDBTwlFbCdWvYXAEwqDT-aeWkJtXxgB_OZ9m1Q130_provenance;
    np:hasPublicationInfo dgn-np:NP244896.RAdYN4wwDBTwlFbCdWvYXAEwqDT-aeWkJtXxgB_OZ9m1Q130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP244896.RAdYN4wwDBTwlFbCdWvYXAEwqDT-aeWkJtXxgB_OZ9m1Q130_assertion a np:Assertion .
  
  dgn-np:NP244896.RAdYN4wwDBTwlFbCdWvYXAEwqDT-aeWkJtXxgB_OZ9m1Q130_provenance a np:Provenance .
  
  dgn-np:NP244896.RAdYN4wwDBTwlFbCdWvYXAEwqDT-aeWkJtXxgB_OZ9m1Q130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP244896.RAdYN4wwDBTwlFbCdWvYXAEwqDT-aeWkJtXxgB_OZ9m1Q130_assertion {
  miriam-gene:7157 a ncit:C16612 .
  
  lld:C0007134 a ncit:C7057 .
  
  dgn-gda:DGNacae9fd28f6e2a9e33b412ef743923c1 sio:SIO_000628 miriam-gene:7157, lld:C0007134;
    a sio:SIO_001121 .
}

dgn-np:NP244896.RAdYN4wwDBTwlFbCdWvYXAEwqDT-aeWkJtXxgB_OZ9m1Q130_provenance {
  dgn-np:NP244896.RAdYN4wwDBTwlFbCdWvYXAEwqDT-aeWkJtXxgB_OZ9m1Q130_assertion dcterms:description
      "[MDM2 expression, combined with increased p53 expression, is associated with reduced survival in several cancers, but is particularly of interest in renal cell carcinoma (RCC) where evidence suggests the presence of tissue-specific p53/MDM2 pathway defects.]. 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:21504894;
    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:NP244896.RAdYN4wwDBTwlFbCdWvYXAEwqDT-aeWkJtXxgB_OZ9m1Q130_publicationInfo {
  this: dcterms:created "2014-10-02T12:34:17+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" .
}