@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP505411.RA6UitB3s0k7IQLqMldkUUxaiv4X_leg7fE4YDsJeZ2fA> .
@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:NP505411.RA6UitB3s0k7IQLqMldkUUxaiv4X_leg7fE4YDsJeZ2fA130_head {
  this: np:hasAssertion dgn-np:NP505411.RA6UitB3s0k7IQLqMldkUUxaiv4X_leg7fE4YDsJeZ2fA130_assertion;
    np:hasProvenance dgn-np:NP505411.RA6UitB3s0k7IQLqMldkUUxaiv4X_leg7fE4YDsJeZ2fA130_provenance;
    np:hasPublicationInfo dgn-np:NP505411.RA6UitB3s0k7IQLqMldkUUxaiv4X_leg7fE4YDsJeZ2fA130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP505411.RA6UitB3s0k7IQLqMldkUUxaiv4X_leg7fE4YDsJeZ2fA130_assertion a np:Assertion .
  
  dgn-np:NP505411.RA6UitB3s0k7IQLqMldkUUxaiv4X_leg7fE4YDsJeZ2fA130_provenance a np:Provenance .
  
  dgn-np:NP505411.RA6UitB3s0k7IQLqMldkUUxaiv4X_leg7fE4YDsJeZ2fA130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP505411.RA6UitB3s0k7IQLqMldkUUxaiv4X_leg7fE4YDsJeZ2fA130_assertion {
  miriam-gene:7157 a ncit:C16612 .
  
  lld:C0035369 a ncit:C7057 .
  
  dgn-gda:DGN3c99144f0dc7a8625cdfc8c5df398d34 sio:SIO_000628 miriam-gene:7157, lld:C0035369;
    a sio:SIO_001121 .
}

dgn-np:NP505411.RA6UitB3s0k7IQLqMldkUUxaiv4X_leg7fE4YDsJeZ2fA130_provenance {
  dgn-np:NP505411.RA6UitB3s0k7IQLqMldkUUxaiv4X_leg7fE4YDsJeZ2fA130_assertion dcterms:description
      "[Whereas transfer of a wild-type p53 expression vector by microinjection or retroviral infection into primary normal human fibroblasts resulted in apoptosis, primary fibroblasts from individuals with xeroderma pigmentosum (XP), who are deficient in DNA repair and have germ-line mutations in the XPB or XPD gene, but not in the XPA or XPC gene, have a deficiency in the apoptotic response.]. 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:8675009;
    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:NP505411.RA6UitB3s0k7IQLqMldkUUxaiv4X_leg7fE4YDsJeZ2fA130_publicationInfo {
  this: dcterms:created "2014-10-02T12:37:01+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" .
}