@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP619027.RAkfiuxXuOU-xtYmv5UMvxLTCd1Km2L1I365c5yd1mYLM> .
@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:NP619027.RAkfiuxXuOU-xtYmv5UMvxLTCd1Km2L1I365c5yd1mYLM130_head {
  this: np:hasAssertion dgn-np:NP619027.RAkfiuxXuOU-xtYmv5UMvxLTCd1Km2L1I365c5yd1mYLM130_assertion;
    np:hasProvenance dgn-np:NP619027.RAkfiuxXuOU-xtYmv5UMvxLTCd1Km2L1I365c5yd1mYLM130_provenance;
    np:hasPublicationInfo dgn-np:NP619027.RAkfiuxXuOU-xtYmv5UMvxLTCd1Km2L1I365c5yd1mYLM130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP619027.RAkfiuxXuOU-xtYmv5UMvxLTCd1Km2L1I365c5yd1mYLM130_assertion a np:Assertion .
  
  dgn-np:NP619027.RAkfiuxXuOU-xtYmv5UMvxLTCd1Km2L1I365c5yd1mYLM130_provenance a np:Provenance .
  
  dgn-np:NP619027.RAkfiuxXuOU-xtYmv5UMvxLTCd1Km2L1I365c5yd1mYLM130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP619027.RAkfiuxXuOU-xtYmv5UMvxLTCd1Km2L1I365c5yd1mYLM130_assertion {
  miriam-gene:4193 a ncit:C16612 .
  
  lld:C0005684 a ncit:C7057 .
  
  dgn-gda:DGNdb7827e7d10c85edfb3d13197cae396f sio:SIO_000628 miriam-gene:4193, lld:C0005684;
    a sio:SIO_001121 .
}

dgn-np:NP619027.RAkfiuxXuOU-xtYmv5UMvxLTCd1Km2L1I365c5yd1mYLM130_provenance {
  dgn-np:NP619027.RAkfiuxXuOU-xtYmv5UMvxLTCd1Km2L1I365c5yd1mYLM130_assertion dcterms:description
      "[This study is the first to report altered patterns of MDM2 expression in human bladder tumors and demonstrates that aberrant Mdm2 and p53 phenotypes may be important diagnostic and prognostic markers in patients affected by bladder cancer.]. 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:8064890;
    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:NP619027.RAkfiuxXuOU-xtYmv5UMvxLTCd1Km2L1I365c5yd1mYLM130_publicationInfo {
  this: dcterms:created "2014-10-02T12:38:14+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" .
}