@prefix dct: <http://purl.org/dc/terms/> .
@prefix orcid: <http://orcid.org/> .
@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP362563.RAB18cPBJb_Qda4Uw_WVXICjcVsQ_fHFzxX7vZU6bglco> .
@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:NP362563.RAB18cPBJb_Qda4Uw_WVXICjcVsQ_fHFzxX7vZU6bglco130_head {
  this: np:hasAssertion dgn-np:NP362563.RAB18cPBJb_Qda4Uw_WVXICjcVsQ_fHFzxX7vZU6bglco130_assertion ;
    np:hasProvenance dgn-np:NP362563.RAB18cPBJb_Qda4Uw_WVXICjcVsQ_fHFzxX7vZU6bglco130_provenance ;
    np:hasPublicationInfo dgn-np:NP362563.RAB18cPBJb_Qda4Uw_WVXICjcVsQ_fHFzxX7vZU6bglco130_publicationInfo ;
    a np:Nanopublication .
  dgn-np:NP362563.RAB18cPBJb_Qda4Uw_WVXICjcVsQ_fHFzxX7vZU6bglco130_assertion a np:Assertion .
  dgn-np:NP362563.RAB18cPBJb_Qda4Uw_WVXICjcVsQ_fHFzxX7vZU6bglco130_provenance a np:Provenance .
  dgn-np:NP362563.RAB18cPBJb_Qda4Uw_WVXICjcVsQ_fHFzxX7vZU6bglco130_publicationInfo a np:PublicationInfo .
}
dgn-np:NP362563.RAB18cPBJb_Qda4Uw_WVXICjcVsQ_fHFzxX7vZU6bglco130_assertion {
  miriam-gene:7376 a ncit:C16612 .
  lld:C0242379 a ncit:C7057 .
  dgn-gda:DGN9a2dc28ef48b64ffbe7cf5a03c06aa1d sio:SIO_000628 miriam-gene:7376 , lld:C0242379 ;
    a sio:SIO_001121 .
}
dgn-np:NP362563.RAB18cPBJb_Qda4Uw_WVXICjcVsQ_fHFzxX7vZU6bglco130_provenance {
  dgn-np:NP362563.RAB18cPBJb_Qda4Uw_WVXICjcVsQ_fHFzxX7vZU6bglco130_assertion dct:description "[Mutations in the DDB2 gene can cause a repair-deficiency syndrome xeroderma pigmentosum group E. Because tobacco carcinogens can cause DNA damage that is repaired by NER and suboptimal NER capacity is reported to be associated with lung cancer risk, we hypothesized that common variants in the DDB2 gene are associated with lung cancer risk.]. 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:16522664 ;
    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:NP362563.RAB18cPBJb_Qda4Uw_WVXICjcVsQ_fHFzxX7vZU6bglco130_publicationInfo {
  this: dct:created "2014-10-02T12:35:32+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" .
}