@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP850169.RA9RE9PkVRxpw78Tg14DH7CBEuNVo7TTGvxhvoC_UfcFk> .
@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:NP850169.RA9RE9PkVRxpw78Tg14DH7CBEuNVo7TTGvxhvoC_UfcFk130_head {
  this: np:hasAssertion dgn-np:NP850169.RA9RE9PkVRxpw78Tg14DH7CBEuNVo7TTGvxhvoC_UfcFk130_assertion ;
    np:hasProvenance dgn-np:NP850169.RA9RE9PkVRxpw78Tg14DH7CBEuNVo7TTGvxhvoC_UfcFk130_provenance ;
    np:hasPublicationInfo dgn-np:NP850169.RA9RE9PkVRxpw78Tg14DH7CBEuNVo7TTGvxhvoC_UfcFk130_publicationInfo ;
    a np:Nanopublication .
  dgn-np:NP850169.RA9RE9PkVRxpw78Tg14DH7CBEuNVo7TTGvxhvoC_UfcFk130_assertion a np:Assertion .
  dgn-np:NP850169.RA9RE9PkVRxpw78Tg14DH7CBEuNVo7TTGvxhvoC_UfcFk130_provenance a np:Provenance .
  dgn-np:NP850169.RA9RE9PkVRxpw78Tg14DH7CBEuNVo7TTGvxhvoC_UfcFk130_publicationInfo a np:PublicationInfo .
}
dgn-np:NP850169.RA9RE9PkVRxpw78Tg14DH7CBEuNVo7TTGvxhvoC_UfcFk130_assertion {
  miriam-gene:1678 a ncit:C16612 .
  lld:C3469521 a ncit:C7057 .
  dgn-gda:DGNd073d2f6d1292eab08f4eb5f1e58d0b7 sio:SIO_000628 miriam-gene:1678 , lld:C3469521 ;
    a sio:SIO_001121 .
}
dgn-np:NP850169.RA9RE9PkVRxpw78Tg14DH7CBEuNVo7TTGvxhvoC_UfcFk130_provenance {
  dgn-np:NP850169.RA9RE9PkVRxpw78Tg14DH7CBEuNVo7TTGvxhvoC_UfcFk130_assertion dcterms:description "[Half of the extracts prepared showed normal levels of in vitro DNA repair synthesis in plasmids containing UV lesions, but the remainder of the extracts from the same cell lines showed deficient repair synthesis, suggesting the possibility of an unusually labile excision repair protein in XP-V. Fanconi's anemia (FA) cells show cellular hypersensitivity to cross-linking agents including cis-DDP.]. 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:2054778 ;
    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:NP850169.RA9RE9PkVRxpw78Tg14DH7CBEuNVo7TTGvxhvoC_UfcFk130_publicationInfo {
  this: dcterms:created "2014-10-02T12:40:39+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" .
}