@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP534322.RAOuTfEYfgFC11UFubQvxIQ0SZVGDGtrghy1duJZKYjS4> .
@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:NP534322.RAOuTfEYfgFC11UFubQvxIQ0SZVGDGtrghy1duJZKYjS4130_head {
   this: np:hasAssertion dgn-np:NP534322.RAOuTfEYfgFC11UFubQvxIQ0SZVGDGtrghy1duJZKYjS4130_assertion ;
    np:hasProvenance dgn-np:NP534322.RAOuTfEYfgFC11UFubQvxIQ0SZVGDGtrghy1duJZKYjS4130_provenance ;
    np:hasPublicationInfo dgn-np:NP534322.RAOuTfEYfgFC11UFubQvxIQ0SZVGDGtrghy1duJZKYjS4130_publicationInfo ;
    a np:Nanopublication .
  dgn-np:NP534322.RAOuTfEYfgFC11UFubQvxIQ0SZVGDGtrghy1duJZKYjS4130_assertion a np:Assertion .
  dgn-np:NP534322.RAOuTfEYfgFC11UFubQvxIQ0SZVGDGtrghy1duJZKYjS4130_provenance a np:Provenance .
  dgn-np:NP534322.RAOuTfEYfgFC11UFubQvxIQ0SZVGDGtrghy1duJZKYjS4130_publicationInfo a np:PublicationInfo .
}
dgn-np:NP534322.RAOuTfEYfgFC11UFubQvxIQ0SZVGDGtrghy1duJZKYjS4130_assertion {
   miriam-gene:3066 a ncit:C16612 .
  lld:C0043346 a ncit:C7057 .
  dgn-gda:DGNc3b2b992e749099908417a74c083b288 sio:SIO_000628 miriam-gene:3066 , lld:C0043346 ;
    a sio:SIO_001121 .
}
dgn-np:NP534322.RAOuTfEYfgFC11UFubQvxIQ0SZVGDGtrghy1duJZKYjS4130_provenance {
   dgn-np:NP534322.RAOuTfEYfgFC11UFubQvxIQ0SZVGDGtrghy1duJZKYjS4130_assertion dcterms:description "[With use of an immortal human cell line (HD2) that expresses excision repair defects typical of XP group D, a series of permanent hybrid cells has been produced with XP cells from groups A to H. Excision repair, as measured by incision analysis and unscheduled DNA synthesis, is restored to normal or near normal levels in crosses involving HD2 and cells from XP groups A, B, C, E, F, G, and I.]. 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:2921028 ;
    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:NP534322.RAOuTfEYfgFC11UFubQvxIQ0SZVGDGtrghy1duJZKYjS4130_publicationInfo {
   this: dcterms:created "2014-10-02T12:37:22+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" .
}