@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP831702.RAAdgzN1psxTlrd-8OK6Ud--UIc02IOIKPZouCuJorW_o> .
@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:NP831702.RAAdgzN1psxTlrd-8OK6Ud--UIc02IOIKPZouCuJorW_o130_head {
  this: np:hasAssertion dgn-np:NP831702.RAAdgzN1psxTlrd-8OK6Ud--UIc02IOIKPZouCuJorW_o130_assertion;
    np:hasProvenance dgn-np:NP831702.RAAdgzN1psxTlrd-8OK6Ud--UIc02IOIKPZouCuJorW_o130_provenance;
    np:hasPublicationInfo dgn-np:NP831702.RAAdgzN1psxTlrd-8OK6Ud--UIc02IOIKPZouCuJorW_o130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP831702.RAAdgzN1psxTlrd-8OK6Ud--UIc02IOIKPZouCuJorW_o130_assertion a np:Assertion .
  
  dgn-np:NP831702.RAAdgzN1psxTlrd-8OK6Ud--UIc02IOIKPZouCuJorW_o130_provenance a np:Provenance .
  
  dgn-np:NP831702.RAAdgzN1psxTlrd-8OK6Ud--UIc02IOIKPZouCuJorW_o130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP831702.RAAdgzN1psxTlrd-8OK6Ud--UIc02IOIKPZouCuJorW_o130_assertion {
  miriam-gene:2068 a ncit:C16612 .
  
  lld:C0023467 a ncit:C7057 .
  
  dgn-gda:DGNe6f89ba4c9dcff384f9be5def5a0ee46 sio:SIO_000628 miriam-gene:2068, lld:C0023467;
    a sio:SIO_001121 .
}

dgn-np:NP831702.RAAdgzN1psxTlrd-8OK6Ud--UIc02IOIKPZouCuJorW_o130_provenance {
  dgn-np:NP831702.RAAdgzN1psxTlrd-8OK6Ud--UIc02IOIKPZouCuJorW_o130_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:NP831702.RAAdgzN1psxTlrd-8OK6Ud--UIc02IOIKPZouCuJorW_o130_publicationInfo {
  this: dcterms:created "2014-10-02T12:40:29+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" .
}