@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP194150.RAXCaSoGAj4kwdQ6MQYxyqoDDTYZV12diT_Xf4sUpn_ys> .
@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:NP194150.RAXCaSoGAj4kwdQ6MQYxyqoDDTYZV12diT_Xf4sUpn_ys130_head {
  this: np:hasAssertion dgn-np:NP194150.RAXCaSoGAj4kwdQ6MQYxyqoDDTYZV12diT_Xf4sUpn_ys130_assertion;
    np:hasProvenance dgn-np:NP194150.RAXCaSoGAj4kwdQ6MQYxyqoDDTYZV12diT_Xf4sUpn_ys130_provenance;
    np:hasPublicationInfo dgn-np:NP194150.RAXCaSoGAj4kwdQ6MQYxyqoDDTYZV12diT_Xf4sUpn_ys130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP194150.RAXCaSoGAj4kwdQ6MQYxyqoDDTYZV12diT_Xf4sUpn_ys130_assertion a np:Assertion .
  
  dgn-np:NP194150.RAXCaSoGAj4kwdQ6MQYxyqoDDTYZV12diT_Xf4sUpn_ys130_provenance a np:Provenance .
  
  dgn-np:NP194150.RAXCaSoGAj4kwdQ6MQYxyqoDDTYZV12diT_Xf4sUpn_ys130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP194150.RAXCaSoGAj4kwdQ6MQYxyqoDDTYZV12diT_Xf4sUpn_ys130_assertion {
  miriam-gene:10721 a ncit:C16612 .
  
  lld:C0006826 a ncit:C7057 .
  
  dgn-gda:DGN75d231bb0d9989fd0a82bc1e91ff25eb sio:SIO_000628 miriam-gene:10721, lld:C0006826;
    a sio:SIO_001121 .
}

dgn-np:NP194150.RAXCaSoGAj4kwdQ6MQYxyqoDDTYZV12diT_Xf4sUpn_ys130_provenance {
  dgn-np:NP194150.RAXCaSoGAj4kwdQ6MQYxyqoDDTYZV12diT_Xf4sUpn_ys130_assertion dcterms:description
      "[XP cells were found to have defects in seven of the proteins of the nucleotide excision repair pathway and in DNA polymerase η. XP cells are hypersensitive to killing by UV radiation, and XP cancers have characteristic `UV signature` mutations.]. 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:22217736;
    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:NP194150.RAXCaSoGAj4kwdQ6MQYxyqoDDTYZV12diT_Xf4sUpn_ys130_publicationInfo {
  this: dcterms:created "2014-10-02T12:33:47+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" .
}