@prefix dct: <http://purl.org/dc/terms/> .
@prefix orcid: <http://orcid.org/> .
@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP44908.RAp-09OdEx61vTtsfqBEK7V1bKWKDB4jueR3nqtG9ersU> .
@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:NP44908.RAp-09OdEx61vTtsfqBEK7V1bKWKDB4jueR3nqtG9ersU130_head {
   this: np:hasAssertion dgn-np:NP44908.RAp-09OdEx61vTtsfqBEK7V1bKWKDB4jueR3nqtG9ersU130_assertion ;
    np:hasProvenance dgn-np:NP44908.RAp-09OdEx61vTtsfqBEK7V1bKWKDB4jueR3nqtG9ersU130_provenance ;
    np:hasPublicationInfo dgn-np:NP44908.RAp-09OdEx61vTtsfqBEK7V1bKWKDB4jueR3nqtG9ersU130_publicationInfo ;
    a np:Nanopublication .
  dgn-np:NP44908.RAp-09OdEx61vTtsfqBEK7V1bKWKDB4jueR3nqtG9ersU130_assertion a np:Assertion .
  dgn-np:NP44908.RAp-09OdEx61vTtsfqBEK7V1bKWKDB4jueR3nqtG9ersU130_provenance a np:Provenance .
  dgn-np:NP44908.RAp-09OdEx61vTtsfqBEK7V1bKWKDB4jueR3nqtG9ersU130_publicationInfo a np:PublicationInfo .
}
dgn-np:NP44908.RAp-09OdEx61vTtsfqBEK7V1bKWKDB4jueR3nqtG9ersU130_assertion {
   miriam-gene:2068 a ncit:C16612 .
  lld:C0005684 a ncit:C7057 .
  dgn-gda:DGN1ba578141ac3055ff8de9121c145085a sio:SIO_000628 miriam-gene:2068 , lld:C0005684 ;
    a sio:SIO_001122 .
}
dgn-np:NP44908.RAp-09OdEx61vTtsfqBEK7V1bKWKDB4jueR3nqtG9ersU130_provenance {
   dgn-np:NP44908.RAp-09OdEx61vTtsfqBEK7V1bKWKDB4jueR3nqtG9ersU130_assertion dct:description "[For other polymorphisms included in this study, NBS1 Glu185Gln, XPD Lys751Gln, XPG Asp1104His, XRCC1 Arg399Gln, XRCC3 Thr241Met, cyclin D1 Pro242Pro, MTHFR Ala222Val and Glu429Ala, NQO1 Arg139Trp and Pro187Ser, no significant differences for genotype distributions and allele frequencies between the bladder cancer cases and the controls were observed in the present study.]. 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:14688016 ;
    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:NP44908.RAp-09OdEx61vTtsfqBEK7V1bKWKDB4jueR3nqtG9ersU130_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" .
}