@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP670547.RAAEMq6Ip4fvBRHtt4VMMxfiIog93Z79c8zJgTTafKLr0> .
@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:NP670547.RAAEMq6Ip4fvBRHtt4VMMxfiIog93Z79c8zJgTTafKLr0130_head {
  this: np:hasAssertion dgn-np:NP670547.RAAEMq6Ip4fvBRHtt4VMMxfiIog93Z79c8zJgTTafKLr0130_assertion;
    np:hasProvenance dgn-np:NP670547.RAAEMq6Ip4fvBRHtt4VMMxfiIog93Z79c8zJgTTafKLr0130_provenance;
    np:hasPublicationInfo dgn-np:NP670547.RAAEMq6Ip4fvBRHtt4VMMxfiIog93Z79c8zJgTTafKLr0130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP670547.RAAEMq6Ip4fvBRHtt4VMMxfiIog93Z79c8zJgTTafKLr0130_assertion a np:Assertion .
  
  dgn-np:NP670547.RAAEMq6Ip4fvBRHtt4VMMxfiIog93Z79c8zJgTTafKLr0130_provenance a np:Provenance .
  
  dgn-np:NP670547.RAAEMq6Ip4fvBRHtt4VMMxfiIog93Z79c8zJgTTafKLr0130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP670547.RAAEMq6Ip4fvBRHtt4VMMxfiIog93Z79c8zJgTTafKLr0130_assertion {
  miriam-gene:8626 a ncit:C16612 .
  
  lld:C0000768 a ncit:C7057 .
  
  dgn-gda:DGN02e415669a3add1cda48a09dceabf398 sio:SIO_000628 miriam-gene:8626, lld:C0000768;
    a sio:SIO_001121 .
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dgn-np:NP670547.RAAEMq6Ip4fvBRHtt4VMMxfiIog93Z79c8zJgTTafKLr0130_provenance {
  dgn-np:NP670547.RAAEMq6Ip4fvBRHtt4VMMxfiIog93Z79c8zJgTTafKLr0130_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-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:NP670547.RAAEMq6Ip4fvBRHtt4VMMxfiIog93Z79c8zJgTTafKLr0130_publicationInfo {
  this: dcterms:created "2014-10-02T12:38:45+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>,
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    pav:version "v2.1.0.0" .
  
  dgn-void:disgenetrdf pav:version "v2.1.0" .
}