@prefix dct: <http://purl.org/dc/terms/> .
@prefix orcid: <http://orcid.org/> .
@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP44921.RAu6CUwgtoWxv1X_opLB-mlEmZZt2CCQhA897YW0T7jzU> .
@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 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:NP44921.RAu6CUwgtoWxv1X_opLB-mlEmZZt2CCQhA897YW0T7jzU130_head {
   this: np:hasAssertion dgn-np:NP44921.RAu6CUwgtoWxv1X_opLB-mlEmZZt2CCQhA897YW0T7jzU130_assertion ;
    np:hasProvenance dgn-np:NP44921.RAu6CUwgtoWxv1X_opLB-mlEmZZt2CCQhA897YW0T7jzU130_provenance ;
    np:hasPublicationInfo dgn-np:NP44921.RAu6CUwgtoWxv1X_opLB-mlEmZZt2CCQhA897YW0T7jzU130_publicationInfo ;
    a np:Nanopublication .
  dgn-np:NP44921.RAu6CUwgtoWxv1X_opLB-mlEmZZt2CCQhA897YW0T7jzU130_assertion a np:Assertion .
  dgn-np:NP44921.RAu6CUwgtoWxv1X_opLB-mlEmZZt2CCQhA897YW0T7jzU130_provenance a np:Provenance .
  dgn-np:NP44921.RAu6CUwgtoWxv1X_opLB-mlEmZZt2CCQhA897YW0T7jzU130_publicationInfo a np:PublicationInfo .
}
dgn-np:NP44921.RAu6CUwgtoWxv1X_opLB-mlEmZZt2CCQhA897YW0T7jzU130_assertion {
   miriam-gene:2068 a ncit:C16612 .
  lld:C0006142 a ncit:C7057 .
  dgn-gda:DGNa7054c3356231cdf5cfd3549ea35d9c0 sio:SIO_000628 miriam-gene:2068 , lld:C0006142 ;
    a sio:SIO_001122 .
}
dgn-np:NP44921.RAu6CUwgtoWxv1X_opLB-mlEmZZt2CCQhA897YW0T7jzU130_provenance {
   dgn-np:NP44921.RAu6CUwgtoWxv1X_opLB-mlEmZZt2CCQhA897YW0T7jzU130_assertion dct:description "[In a nested case-control study of breast cancer in US radiologic technologists exposed to low levels of ionizing radiation (858 cases, 1,083 controls), we examined whether risk of breast cancer conferred by radiation was modified by nucleotide excision gene polymorphisms ERCC2 (XPD) rs13181, ERCC4 (XPF) rs1800067 and rs1800124, ERCC5 (XPG) rs1047769 and rs17655; and ERCC6 rs2228526.]. 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:18767034 ;
    prov:wasDerivedFrom dgn-void:gad-20130706 ;
    prov:wasGeneratedBy eco:ECO_0000203 .
  dgn-void:gad-20130706 pav:importedOn "2013-07-06"^^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:NP44921.RAu6CUwgtoWxv1X_opLB-mlEmZZt2CCQhA897YW0T7jzU130_publicationInfo {
   this: dct:created "2014-10-02T12:32:20+02:00"^^xsd:dateTime ;
    dct:rights <http://opendatacommons.org/licenses/odbl/1.0/> ;
    dct:rightsHolder dgn-void:IBIGroup ;
    dct:subject sio:SIO_000983 ;
    prv:usedData dgn-void:disgenetrdf ;
    pav:authoredBy orcid:0000-0001-5999-6269 , orcid:0000-0002-7534-7661 , orcid:0000-0002-9383-528X , orcid:0000-0003-0169-8159 , orcid:0000-0003-1244-7654 ;
    pav:createdBy orcid:0000-0003-0169-8159 ;
    pav:version "v2.1.0.0" .
  dgn-void:disgenetrdf pav:version "v2.1.0" .
}