@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP460058.RAuzC2wwnhU66tXOFnn3KXKUuXtmTbvaOAMF3-cvelcIE> .
@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:NP460058.RAuzC2wwnhU66tXOFnn3KXKUuXtmTbvaOAMF3-cvelcIE130_head {
  this: np:hasAssertion dgn-np:NP460058.RAuzC2wwnhU66tXOFnn3KXKUuXtmTbvaOAMF3-cvelcIE130_assertion;
    np:hasProvenance dgn-np:NP460058.RAuzC2wwnhU66tXOFnn3KXKUuXtmTbvaOAMF3-cvelcIE130_provenance;
    np:hasPublicationInfo dgn-np:NP460058.RAuzC2wwnhU66tXOFnn3KXKUuXtmTbvaOAMF3-cvelcIE130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP460058.RAuzC2wwnhU66tXOFnn3KXKUuXtmTbvaOAMF3-cvelcIE130_assertion a np:Assertion .
  
  dgn-np:NP460058.RAuzC2wwnhU66tXOFnn3KXKUuXtmTbvaOAMF3-cvelcIE130_provenance a np:Provenance .
  
  dgn-np:NP460058.RAuzC2wwnhU66tXOFnn3KXKUuXtmTbvaOAMF3-cvelcIE130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP460058.RAuzC2wwnhU66tXOFnn3KXKUuXtmTbvaOAMF3-cvelcIE130_assertion {
  miriam-gene:4193 a ncit:C16612 .
  
  lld:C0007097 a ncit:C7057 .
  
  dgn-gda:DGN1de8451db12c6245caf09c8ec594f394 sio:SIO_000628 miriam-gene:4193, lld:C0007097;
    a sio:SIO_001121 .
}

dgn-np:NP460058.RAuzC2wwnhU66tXOFnn3KXKUuXtmTbvaOAMF3-cvelcIE130_provenance {
  dgn-np:NP460058.RAuzC2wwnhU66tXOFnn3KXKUuXtmTbvaOAMF3-cvelcIE130_assertion dcterms:description
      "[In view of the significance of MDM2 as a regulator as well as critical target of wild type p53, this study was undertaken to determine the alteration in MDM2 expression in esophageal squamons cell carcinoma (ESCC) and its relationship to clinicopathological parameters as well as p53gene and protein status.]. 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:11692147;
    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:NP460058.RAuzC2wwnhU66tXOFnn3KXKUuXtmTbvaOAMF3-cvelcIE130_publicationInfo {
  this: dcterms:created "2014-10-02T12:36:34+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" .
}