@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP118488.RAdvXdq-dBnTbUxWXvSKLU8acaq96AevFFmglgRUZfgFM> .
@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:NP118488.RAdvXdq-dBnTbUxWXvSKLU8acaq96AevFFmglgRUZfgFM130_head {
  this: np:hasAssertion dgn-np:NP118488.RAdvXdq-dBnTbUxWXvSKLU8acaq96AevFFmglgRUZfgFM130_assertion;
    np:hasProvenance dgn-np:NP118488.RAdvXdq-dBnTbUxWXvSKLU8acaq96AevFFmglgRUZfgFM130_provenance;
    np:hasPublicationInfo dgn-np:NP118488.RAdvXdq-dBnTbUxWXvSKLU8acaq96AevFFmglgRUZfgFM130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP118488.RAdvXdq-dBnTbUxWXvSKLU8acaq96AevFFmglgRUZfgFM130_assertion a np:Assertion .
  
  dgn-np:NP118488.RAdvXdq-dBnTbUxWXvSKLU8acaq96AevFFmglgRUZfgFM130_provenance a np:Provenance .
  
  dgn-np:NP118488.RAdvXdq-dBnTbUxWXvSKLU8acaq96AevFFmglgRUZfgFM130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP118488.RAdvXdq-dBnTbUxWXvSKLU8acaq96AevFFmglgRUZfgFM130_assertion {
  miriam-gene:7157 a ncit:C16612 .
  
  lld:C0025202 a ncit:C7057 .
  
  dgn-gda:DGN565ef42fb393b1372e28154222d267fb sio:SIO_000628 miriam-gene:7157, lld:C0025202;
    a sio:SIO_001123 .
}

dgn-np:NP118488.RAdvXdq-dBnTbUxWXvSKLU8acaq96AevFFmglgRUZfgFM130_provenance {
  dgn-np:NP118488.RAdvXdq-dBnTbUxWXvSKLU8acaq96AevFFmglgRUZfgFM130_assertion dcterms:description
      "[p53 alterations commence as early as at the stage of benign and dysplastic nevi but there is no concordance between the frequent p53 protein expression and the rarity of both TP53 gene mutations in melanomas.]. 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:15557758;
    prov:wasDerivedFrom dgn-void:lhgdn-20090331;
    prov:wasGeneratedBy eco:ECO_0000203 .
  
  dgn-void:lhgdn-20090331 pav:importedOn "2009-03-31"^^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:NP118488.RAdvXdq-dBnTbUxWXvSKLU8acaq96AevFFmglgRUZfgFM130_publicationInfo {
  this: dcterms:created "2014-10-02T12:33:01+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" .
}