@prefix this: <http://rdf.disgenet.org/resource/nanopub/NP1386736.RAEDOM-yFOGVjlboWr3mGZaujDhM12EUkGZDMIX_66ZNg> .
@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:NP1386736.RAEDOM-yFOGVjlboWr3mGZaujDhM12EUkGZDMIX_66ZNg130_head {
  this: np:hasAssertion dgn-np:NP1386736.RAEDOM-yFOGVjlboWr3mGZaujDhM12EUkGZDMIX_66ZNg130_assertion;
    np:hasProvenance dgn-np:NP1386736.RAEDOM-yFOGVjlboWr3mGZaujDhM12EUkGZDMIX_66ZNg130_provenance;
    np:hasPublicationInfo dgn-np:NP1386736.RAEDOM-yFOGVjlboWr3mGZaujDhM12EUkGZDMIX_66ZNg130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP1386736.RAEDOM-yFOGVjlboWr3mGZaujDhM12EUkGZDMIX_66ZNg130_assertion a np:Assertion .
  
  dgn-np:NP1386736.RAEDOM-yFOGVjlboWr3mGZaujDhM12EUkGZDMIX_66ZNg130_provenance a np:Provenance .
  
  dgn-np:NP1386736.RAEDOM-yFOGVjlboWr3mGZaujDhM12EUkGZDMIX_66ZNg130_publicationInfo
    a np:PublicationInfo .
}

dgn-np:NP1386736.RAEDOM-yFOGVjlboWr3mGZaujDhM12EUkGZDMIX_66ZNg130_assertion {
  miriam-gene:2068 a ncit:C16612 .
  
  lld:C0268138 a ncit:C7057 .
  
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dgn-np:NP1386736.RAEDOM-yFOGVjlboWr3mGZaujDhM12EUkGZDMIX_66ZNg130_provenance {
  dgn-np:NP1386736.RAEDOM-yFOGVjlboWr3mGZaujDhM12EUkGZDMIX_66ZNg130_assertion dcterms:description
      "[These results establish the essential function of the XPD protein in mammals and in cellular viability and are consistent with the notion that only subtle XPD mutations are found in XP, XP/Cockayne syndrome, and trichothiodystrophy patients.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine."@en;
    wi:evidence dgn-void:source_evidence_literature;
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    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:NP1386736.RAEDOM-yFOGVjlboWr3mGZaujDhM12EUkGZDMIX_66ZNg130_publicationInfo {
  this: dcterms:created "2016-05-13T12:52:14+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>,
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    pav:createdBy <http://orcid.org/0000-0003-0169-8159>;
    pav:version "v4.0.0.0" .
  
  dgn-void:disgenetv3.0rdf pav:version "v4.0.0" .
}