@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP343298.RA2bEqsRb5WXHqD8EkGNuqz-QFdvpIOYmAi8h6fDYJSuU> .
@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:NP343298.RA2bEqsRb5WXHqD8EkGNuqz-QFdvpIOYmAi8h6fDYJSuU130_head {
  this: np:hasAssertion dgn-np:NP343298.RA2bEqsRb5WXHqD8EkGNuqz-QFdvpIOYmAi8h6fDYJSuU130_assertion;
    np:hasProvenance dgn-np:NP343298.RA2bEqsRb5WXHqD8EkGNuqz-QFdvpIOYmAi8h6fDYJSuU130_provenance;
    np:hasPublicationInfo dgn-np:NP343298.RA2bEqsRb5WXHqD8EkGNuqz-QFdvpIOYmAi8h6fDYJSuU130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP343298.RA2bEqsRb5WXHqD8EkGNuqz-QFdvpIOYmAi8h6fDYJSuU130_assertion a np:Assertion .
  
  dgn-np:NP343298.RA2bEqsRb5WXHqD8EkGNuqz-QFdvpIOYmAi8h6fDYJSuU130_provenance a np:Provenance .
  
  dgn-np:NP343298.RA2bEqsRb5WXHqD8EkGNuqz-QFdvpIOYmAi8h6fDYJSuU130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP343298.RA2bEqsRb5WXHqD8EkGNuqz-QFdvpIOYmAi8h6fDYJSuU130_assertion {
  miriam-gene:7157 a ncit:C16612 .
  
  lld:C0001624 a ncit:C7057 .
  
  dgn-gda:DGNb0ced9e5564fc7524512b0dde45d40c9 sio:SIO_000628 miriam-gene:7157, lld:C0001624;
    a sio:SIO_001121 .
}

dgn-np:NP343298.RA2bEqsRb5WXHqD8EkGNuqz-QFdvpIOYmAi8h6fDYJSuU130_provenance {
  dgn-np:NP343298.RA2bEqsRb5WXHqD8EkGNuqz-QFdvpIOYmAi8h6fDYJSuU130_assertion dcterms:description
      "[As p53 protein is a regulator of guanine nucleotide synthesis, the loss of normal inhibitory regulation by the p53 mutation would serve to increase the availability of GTP for the transduction of signals essential for increased cell growth and hormone expression in the adrenal tumors.]. 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:8106638;
    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:NP343298.RA2bEqsRb5WXHqD8EkGNuqz-QFdvpIOYmAi8h6fDYJSuU130_publicationInfo {
  this: dcterms:created "2014-10-02T12:35:22+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" .
}