@prefix this: <http://rdf.disgenet.org/resource/nanopub/NP818370.RADW95fqJ8VJ3YO1q12CDEVqX2c6a45xynHJh58A9eaiA> .
@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/> .
@prefix wi: <http://purl.org/ontology/wi/core#> .
@prefix prov: <http://www.w3.org/ns/prov#> .
@prefix pav: <http://purl.org/pav/> .
@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/resource/nanopub/> .
@prefix dgn-gda: <http://rdf.disgenet.org/resource/gda/> .
@prefix dgn-void: <http://rdf.disgenet.org/v4.0.0/void/> .

dgn-np:NP818370.RADW95fqJ8VJ3YO1q12CDEVqX2c6a45xynHJh58A9eaiA130_head {
  this: np:hasAssertion dgn-np:NP818370.RADW95fqJ8VJ3YO1q12CDEVqX2c6a45xynHJh58A9eaiA130_assertion;
    np:hasProvenance dgn-np:NP818370.RADW95fqJ8VJ3YO1q12CDEVqX2c6a45xynHJh58A9eaiA130_provenance;
    np:hasPublicationInfo dgn-np:NP818370.RADW95fqJ8VJ3YO1q12CDEVqX2c6a45xynHJh58A9eaiA130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP818370.RADW95fqJ8VJ3YO1q12CDEVqX2c6a45xynHJh58A9eaiA130_assertion a np:Assertion .
  
  dgn-np:NP818370.RADW95fqJ8VJ3YO1q12CDEVqX2c6a45xynHJh58A9eaiA130_provenance a np:Provenance .
  
  dgn-np:NP818370.RADW95fqJ8VJ3YO1q12CDEVqX2c6a45xynHJh58A9eaiA130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP818370.RADW95fqJ8VJ3YO1q12CDEVqX2c6a45xynHJh58A9eaiA130_assertion {
  miriam-gene:7405 a ncit:C16612 .
  
  lld:C0000768 a ncit:C7057 .
  
  dgn-gda:DGNbd6804df91ef212b109b121b33cee6fb sio:SIO_000628 miriam-gene:7405, lld:C0000768;
    a sio:SIO_001121 .
}

dgn-np:NP818370.RADW95fqJ8VJ3YO1q12CDEVqX2c6a45xynHJh58A9eaiA130_provenance {
  dgn-np:NP818370.RADW95fqJ8VJ3YO1q12CDEVqX2c6a45xynHJh58A9eaiA130_assertion dcterms:description
      "[As mutants of p63 in humans exhibit phenotypes that cause several autosomal dominantly inherited syndromes leading to developmental malformations, we tested the transcriptional response of TAp63γ mutants derived from the EEC, SHFM and ADULT syndromes.]. 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:20543567;
    prov:wasDerivedFrom dgn-void:befree-2016;
    prov:wasGeneratedBy eco:ECO_0000203 .
  
  dgn-void:befree-2016 pav:importedOn "2016-02-19"^^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:NP818370.RADW95fqJ8VJ3YO1q12CDEVqX2c6a45xynHJh58A9eaiA130_publicationInfo {
  this: dcterms:created "2016-05-13T12:47:56+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:disgenetv3.0rdf;
    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 "v4.0.0.0" .
  
  dgn-void:disgenetv3.0rdf pav:version "v4.0.0" .
}