@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP299250.RATRRK0dbt70EqR3lDpQwJ9BUKYJgfDblm1UzHEmgLFIA> .
@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:NP299250.RATRRK0dbt70EqR3lDpQwJ9BUKYJgfDblm1UzHEmgLFIA130_head {
   this: np:hasAssertion dgn-np:NP299250.RATRRK0dbt70EqR3lDpQwJ9BUKYJgfDblm1UzHEmgLFIA130_assertion ;
    np:hasProvenance dgn-np:NP299250.RATRRK0dbt70EqR3lDpQwJ9BUKYJgfDblm1UzHEmgLFIA130_provenance ;
    np:hasPublicationInfo dgn-np:NP299250.RATRRK0dbt70EqR3lDpQwJ9BUKYJgfDblm1UzHEmgLFIA130_publicationInfo ;
    a np:Nanopublication .
  dgn-np:NP299250.RATRRK0dbt70EqR3lDpQwJ9BUKYJgfDblm1UzHEmgLFIA130_assertion a np:Assertion .
  dgn-np:NP299250.RATRRK0dbt70EqR3lDpQwJ9BUKYJgfDblm1UzHEmgLFIA130_provenance a np:Provenance .
  dgn-np:NP299250.RATRRK0dbt70EqR3lDpQwJ9BUKYJgfDblm1UzHEmgLFIA130_publicationInfo a np:PublicationInfo .
}
dgn-np:NP299250.RATRRK0dbt70EqR3lDpQwJ9BUKYJgfDblm1UzHEmgLFIA130_assertion {
   miriam-gene:4524 a ncit:C16612 .
  lld:C0268138 a ncit:C7057 .
  dgn-gda:DGNfa13438bb50689880efc2acc1d46046f sio:SIO_000628 miriam-gene:4524 , lld:C0268138 ;
    a sio:SIO_001121 .
}
dgn-np:NP299250.RATRRK0dbt70EqR3lDpQwJ9BUKYJgfDblm1UzHEmgLFIA130_provenance {
   dgn-np:NP299250.RATRRK0dbt70EqR3lDpQwJ9BUKYJgfDblm1UzHEmgLFIA130_assertion dcterms:description "[Some evidence exists for the effects of X-ray cross complementation group 1 (XRCC1) codon 280 and (in smokers) Xeroderma pigmentosum group D (XPD) codon 23 polymorphisms on baseline CAs, for XRCC1 codon 399 polymorphism on SCEs in smokers, and for methylene tetrahydrofolate reductase (MTHFR) codon 677 and methionine synthase reductase (MTRR) polymorphisms on spontaneous MN.]. 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:15093278 ;
    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:NP299250.RATRRK0dbt70EqR3lDpQwJ9BUKYJgfDblm1UzHEmgLFIA130_publicationInfo {
   this: dcterms:created "2014-10-02T12:34:50+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" .
}