@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP871973.RAa3QjdWL94RwYwzrQQslgXYH2l5UsteeuSo7T5KOPUXw> .
@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:NP871973.RAa3QjdWL94RwYwzrQQslgXYH2l5UsteeuSo7T5KOPUXw130_head {
  this: np:hasAssertion dgn-np:NP871973.RAa3QjdWL94RwYwzrQQslgXYH2l5UsteeuSo7T5KOPUXw130_assertion;
    np:hasProvenance dgn-np:NP871973.RAa3QjdWL94RwYwzrQQslgXYH2l5UsteeuSo7T5KOPUXw130_provenance;
    np:hasPublicationInfo dgn-np:NP871973.RAa3QjdWL94RwYwzrQQslgXYH2l5UsteeuSo7T5KOPUXw130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP871973.RAa3QjdWL94RwYwzrQQslgXYH2l5UsteeuSo7T5KOPUXw130_assertion a np:Assertion .
  
  dgn-np:NP871973.RAa3QjdWL94RwYwzrQQslgXYH2l5UsteeuSo7T5KOPUXw130_provenance a np:Provenance .
  
  dgn-np:NP871973.RAa3QjdWL94RwYwzrQQslgXYH2l5UsteeuSo7T5KOPUXw130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP871973.RAa3QjdWL94RwYwzrQQslgXYH2l5UsteeuSo7T5KOPUXw130_assertion {
  miriam-gene:8626 a ncit:C16612 .
  
  lld:C0000768 a ncit:C7057 .
  
  dgn-gda:DGNf0dd898aa428a5e164c655a4035a19e2 sio:SIO_000628 miriam-gene:8626, lld:C0000768;
    a sio:SIO_001121 .
}

dgn-np:NP871973.RAa3QjdWL94RwYwzrQQslgXYH2l5UsteeuSo7T5KOPUXw130_provenance {
  dgn-np:NP871973.RAa3QjdWL94RwYwzrQQslgXYH2l5UsteeuSo7T5KOPUXw130_assertion dcterms:description
      "[We point out common themes and features, that allow to speculate on the possible role of p63 downstream events and their potential exploitation in future attempts to correct the congenital defect in preclinical studies.]. 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:21716671;
    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:NP871973.RAa3QjdWL94RwYwzrQQslgXYH2l5UsteeuSo7T5KOPUXw130_publicationInfo {
  this: dcterms:created "2014-10-02T12:40:53+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" .
}