@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP761165.RAmdsfH7HCQRChey8areQaHLeBQr3C5dcv53SODHihbb4> .
@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:NP761165.RAmdsfH7HCQRChey8areQaHLeBQr3C5dcv53SODHihbb4130_head {
  this: np:hasAssertion dgn-np:NP761165.RAmdsfH7HCQRChey8areQaHLeBQr3C5dcv53SODHihbb4130_assertion;
    np:hasProvenance dgn-np:NP761165.RAmdsfH7HCQRChey8areQaHLeBQr3C5dcv53SODHihbb4130_provenance;
    np:hasPublicationInfo dgn-np:NP761165.RAmdsfH7HCQRChey8areQaHLeBQr3C5dcv53SODHihbb4130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP761165.RAmdsfH7HCQRChey8areQaHLeBQr3C5dcv53SODHihbb4130_assertion a np:Assertion .
  
  dgn-np:NP761165.RAmdsfH7HCQRChey8areQaHLeBQr3C5dcv53SODHihbb4130_provenance a np:Provenance .
  
  dgn-np:NP761165.RAmdsfH7HCQRChey8areQaHLeBQr3C5dcv53SODHihbb4130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP761165.RAmdsfH7HCQRChey8areQaHLeBQr3C5dcv53SODHihbb4130_assertion {
  miriam-gene:2944 a ncit:C16612 .
  
  lld:C0019156 a ncit:C7057 .
  
  dgn-gda:DGNd6ea3bf2c14ad2fa80fbc4b3383cb529 sio:SIO_000628 miriam-gene:2944, lld:C0019156;
    a sio:SIO_001121 .
}

dgn-np:NP761165.RAmdsfH7HCQRChey8areQaHLeBQr3C5dcv53SODHihbb4130_provenance {
  dgn-np:NP761165.RAmdsfH7HCQRChey8areQaHLeBQr3C5dcv53SODHihbb4130_assertion dcterms:description
      "[The present study integrated clinical data regarding the occurrence of HVOD, graft versus host disease (GVHD), BU pharmacokinetics and GSTA1, GSTP1, GSTM1, and GSTT1 genotypes of 18 children who received BU in their pre-HSCT conditioning regimen.]. 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:20672371;
    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:NP761165.RAmdsfH7HCQRChey8areQaHLeBQr3C5dcv53SODHihbb4130_publicationInfo {
  this: dcterms:created "2014-10-02T12:39:40+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" .
}