@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP422220.RAvpRrWXN9IZJQ31QTiZLN8zRGBrbUTTqGb6uWAXGzcYA> .
@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:NP422220.RAvpRrWXN9IZJQ31QTiZLN8zRGBrbUTTqGb6uWAXGzcYA130_head {
  this: np:hasAssertion dgn-np:NP422220.RAvpRrWXN9IZJQ31QTiZLN8zRGBrbUTTqGb6uWAXGzcYA130_assertion;
    np:hasProvenance dgn-np:NP422220.RAvpRrWXN9IZJQ31QTiZLN8zRGBrbUTTqGb6uWAXGzcYA130_provenance;
    np:hasPublicationInfo dgn-np:NP422220.RAvpRrWXN9IZJQ31QTiZLN8zRGBrbUTTqGb6uWAXGzcYA130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP422220.RAvpRrWXN9IZJQ31QTiZLN8zRGBrbUTTqGb6uWAXGzcYA130_assertion a np:Assertion .
  
  dgn-np:NP422220.RAvpRrWXN9IZJQ31QTiZLN8zRGBrbUTTqGb6uWAXGzcYA130_provenance a np:Provenance .
  
  dgn-np:NP422220.RAvpRrWXN9IZJQ31QTiZLN8zRGBrbUTTqGb6uWAXGzcYA130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP422220.RAvpRrWXN9IZJQ31QTiZLN8zRGBrbUTTqGb6uWAXGzcYA130_assertion {
  miriam-gene:7157 a ncit:C16612 .
  
  lld:C0231341 a ncit:C7057 .
  
  dgn-gda:DGNa1ff12d5e25d0584fc6abed6022c1c96 sio:SIO_000628 miriam-gene:7157, lld:C0231341;
    a sio:SIO_001121 .
}

dgn-np:NP422220.RAvpRrWXN9IZJQ31QTiZLN8zRGBrbUTTqGb6uWAXGzcYA130_provenance {
  dgn-np:NP422220.RAvpRrWXN9IZJQ31QTiZLN8zRGBrbUTTqGb6uWAXGzcYA130_assertion dcterms:description
      "[The shorter isoform regulates full length p53 and in cases where there is too much of the longer isoform, this leads to elevated apoptosis resulting in decreased tumor incidence but also in premature ageing due to exhaustion of the renewal potential.]. 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:17471501;
    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:NP422220.RAvpRrWXN9IZJQ31QTiZLN8zRGBrbUTTqGb6uWAXGzcYA130_publicationInfo {
  this: dcterms:created "2014-10-02T12:36:10+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" .
}