@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP275034.RAyVyRCGS4dbCU1rNbK93Exr1rtvp_QR_iL8_e5766Ja8> .
@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:NP275034.RAyVyRCGS4dbCU1rNbK93Exr1rtvp_QR_iL8_e5766Ja8130_head {
  this: np:hasAssertion dgn-np:NP275034.RAyVyRCGS4dbCU1rNbK93Exr1rtvp_QR_iL8_e5766Ja8130_assertion ;
    np:hasProvenance dgn-np:NP275034.RAyVyRCGS4dbCU1rNbK93Exr1rtvp_QR_iL8_e5766Ja8130_provenance ;
    np:hasPublicationInfo dgn-np:NP275034.RAyVyRCGS4dbCU1rNbK93Exr1rtvp_QR_iL8_e5766Ja8130_publicationInfo ;
    a np:Nanopublication .
  dgn-np:NP275034.RAyVyRCGS4dbCU1rNbK93Exr1rtvp_QR_iL8_e5766Ja8130_assertion a np:Assertion .
  dgn-np:NP275034.RAyVyRCGS4dbCU1rNbK93Exr1rtvp_QR_iL8_e5766Ja8130_provenance a np:Provenance .
  dgn-np:NP275034.RAyVyRCGS4dbCU1rNbK93Exr1rtvp_QR_iL8_e5766Ja8130_publicationInfo a np:PublicationInfo .
}
dgn-np:NP275034.RAyVyRCGS4dbCU1rNbK93Exr1rtvp_QR_iL8_e5766Ja8130_assertion {
  miriam-gene:328 a ncit:C16612 .
  lld:C0006826 a ncit:C7057 .
  dgn-gda:DGN276340311e952ddfcc73fc6570fbb3a4 sio:SIO_000628 miriam-gene:328 , lld:C0006826 ;
    a sio:SIO_001121 .
}
dgn-np:NP275034.RAyVyRCGS4dbCU1rNbK93Exr1rtvp_QR_iL8_e5766Ja8130_provenance {
  dgn-np:NP275034.RAyVyRCGS4dbCU1rNbK93Exr1rtvp_QR_iL8_e5766Ja8130_assertion dcterms:description "[The previously reported association of the APEX Asp148Glu single nucleotide polymorphism (SNP) with cancer, and the suggestion of associations of the XRCC3 Thr241Met and hOGG1 Ser326Cys SNP sites with G(2) chromosomal radiosensitivity were investigated in a new study of 30 childhood and young adult cancer survivors, their 30 partners, and 55 offspring.]. 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:21113933 ;
    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:NP275034.RAyVyRCGS4dbCU1rNbK93Exr1rtvp_QR_iL8_e5766Ja8130_publicationInfo {
  this: dcterms:created "2014-10-02T12:34:35+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" .
}