@prefix this: <http://rdf.disgenet.org/resource/nanopub/NP158998.RAMhCx_xMx6o_51hWxGVQRxE1pGgdnMt55RJg4ZLUho6I> .
@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/> .
@prefix wi: <http://purl.org/ontology/wi/core#> .
@prefix prov: <http://www.w3.org/ns/prov#> .
@prefix pav: <http://purl.org/pav/> .
@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/resource/nanopub/> .
@prefix dgn-gda: <http://rdf.disgenet.org/resource/gda/> .
@prefix dgn-void: <http://rdf.disgenet.org/v3.0.0/void/> .
dgn-np:NP158998.RAMhCx_xMx6o_51hWxGVQRxE1pGgdnMt55RJg4ZLUho6I130_head {
  this: np:hasAssertion dgn-np:NP158998.RAMhCx_xMx6o_51hWxGVQRxE1pGgdnMt55RJg4ZLUho6I130_assertion ;
    np:hasProvenance dgn-np:NP158998.RAMhCx_xMx6o_51hWxGVQRxE1pGgdnMt55RJg4ZLUho6I130_provenance ;
    np:hasPublicationInfo dgn-np:NP158998.RAMhCx_xMx6o_51hWxGVQRxE1pGgdnMt55RJg4ZLUho6I130_publicationInfo ;
    a np:Nanopublication .
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  dgn-np:NP158998.RAMhCx_xMx6o_51hWxGVQRxE1pGgdnMt55RJg4ZLUho6I130_provenance a np:Provenance .
  dgn-np:NP158998.RAMhCx_xMx6o_51hWxGVQRxE1pGgdnMt55RJg4ZLUho6I130_publicationInfo a np:PublicationInfo .
}
dgn-np:NP158998.RAMhCx_xMx6o_51hWxGVQRxE1pGgdnMt55RJg4ZLUho6I130_assertion {
  miriam-gene:81569 a ncit:C16612 .
  lld:C0242350 a ncit:C7057 .
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    a sio:SIO_001122 .
}
dgn-np:NP158998.RAMhCx_xMx6o_51hWxGVQRxE1pGgdnMt55RJg4ZLUho6I130_provenance {
  dgn-np:NP158998.RAMhCx_xMx6o_51hWxGVQRxE1pGgdnMt55RJg4ZLUho6I130_assertion dcterms:description "[To our knowledge, this is the first genome-wide association study to identify SNPs associated with adverse effects resulting from radiotherapy. It is important to note that the SNP that proved to be significantly associated with ED is located within a gen]. 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:20932654 ;
    prov:wasDerivedFrom dgn-void:gad-20150221 ;
    prov:wasGeneratedBy eco:ECO_0000203 .
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  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:NP158998.RAMhCx_xMx6o_51hWxGVQRxE1pGgdnMt55RJg4ZLUho6I130_publicationInfo {
  this: dcterms:created "2015-08-25T14:39:10+02:00"^^xsd:dateTime ;
    dcterms:rights <http://opendatacommons.org/licenses/odbl/1.0/> ;
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}