@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP897238.RA1kFDR-hBLSUiP4vajrSMjziiduYdqJq6uMkrBljfAIo> .
@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:NP897238.RA1kFDR-hBLSUiP4vajrSMjziiduYdqJq6uMkrBljfAIo130_head {
  this: np:hasAssertion dgn-np:NP897238.RA1kFDR-hBLSUiP4vajrSMjziiduYdqJq6uMkrBljfAIo130_assertion ;
    np:hasProvenance dgn-np:NP897238.RA1kFDR-hBLSUiP4vajrSMjziiduYdqJq6uMkrBljfAIo130_provenance ;
    np:hasPublicationInfo dgn-np:NP897238.RA1kFDR-hBLSUiP4vajrSMjziiduYdqJq6uMkrBljfAIo130_publicationInfo ;
    a np:Nanopublication .
  dgn-np:NP897238.RA1kFDR-hBLSUiP4vajrSMjziiduYdqJq6uMkrBljfAIo130_assertion a np:Assertion .
  dgn-np:NP897238.RA1kFDR-hBLSUiP4vajrSMjziiduYdqJq6uMkrBljfAIo130_provenance a np:Provenance .
  dgn-np:NP897238.RA1kFDR-hBLSUiP4vajrSMjziiduYdqJq6uMkrBljfAIo130_publicationInfo a np:PublicationInfo .
}
dgn-np:NP897238.RA1kFDR-hBLSUiP4vajrSMjziiduYdqJq6uMkrBljfAIo130_assertion {
  miriam-gene:7507 a ncit:C16612 .
  lld:C0023467 a ncit:C7057 .
  dgn-gda:DGNd4504f5f116c8257936c10dbc2ed7022 sio:SIO_000628 miriam-gene:7507 , lld:C0023467 ;
    a sio:SIO_001121 .
}
dgn-np:NP897238.RA1kFDR-hBLSUiP4vajrSMjziiduYdqJq6uMkrBljfAIo130_provenance {
  dgn-np:NP897238.RA1kFDR-hBLSUiP4vajrSMjziiduYdqJq6uMkrBljfAIo130_assertion dcterms:description "[Additionally, polymorphisms of the XPA, XPD, XRCC1, XRCC3 and RAD51 DNA repair genes revealed three unfavorable alleles with low DNA repair capacity.In summary, we report the first case of AML involving XPD and XRCC3 polymorphisms from donor origin following allogeneic stem cell transplantation and highlight the potential need for careful analysis of DNA repair gene polymorphisms in selecting candidate donors prior to allogeneic stem cell transplantation.]. 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:21951951 ;
    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:NP897238.RA1kFDR-hBLSUiP4vajrSMjziiduYdqJq6uMkrBljfAIo130_publicationInfo {
  this: dcterms:created "2014-10-02T12:41:11+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" .
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}