@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP635610.RAa2FI5AFpxmTYUHlOLbGKK53mwfB5eho4eTtHTfYXOBY> .
@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:NP635610.RAa2FI5AFpxmTYUHlOLbGKK53mwfB5eho4eTtHTfYXOBY130_head {
  this: np:hasAssertion dgn-np:NP635610.RAa2FI5AFpxmTYUHlOLbGKK53mwfB5eho4eTtHTfYXOBY130_assertion;
    np:hasProvenance dgn-np:NP635610.RAa2FI5AFpxmTYUHlOLbGKK53mwfB5eho4eTtHTfYXOBY130_provenance;
    np:hasPublicationInfo dgn-np:NP635610.RAa2FI5AFpxmTYUHlOLbGKK53mwfB5eho4eTtHTfYXOBY130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP635610.RAa2FI5AFpxmTYUHlOLbGKK53mwfB5eho4eTtHTfYXOBY130_assertion a np:Assertion .
  
  dgn-np:NP635610.RAa2FI5AFpxmTYUHlOLbGKK53mwfB5eho4eTtHTfYXOBY130_provenance a np:Provenance .
  
  dgn-np:NP635610.RAa2FI5AFpxmTYUHlOLbGKK53mwfB5eho4eTtHTfYXOBY130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP635610.RAa2FI5AFpxmTYUHlOLbGKK53mwfB5eho4eTtHTfYXOBY130_assertion {
  miriam-gene:2952 a ncit:C16612 .
  
  lld:C0019156 a ncit:C7057 .
  
  dgn-gda:DGNc0ca9d3bcf07e0395751ad4b86dfad72 sio:SIO_000628 miriam-gene:2952, lld:C0019156;
    a sio:SIO_001121 .
}

dgn-np:NP635610.RAa2FI5AFpxmTYUHlOLbGKK53mwfB5eho4eTtHTfYXOBY130_provenance {
  dgn-np:NP635610.RAa2FI5AFpxmTYUHlOLbGKK53mwfB5eho4eTtHTfYXOBY130_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:NP635610.RAa2FI5AFpxmTYUHlOLbGKK53mwfB5eho4eTtHTfYXOBY130_publicationInfo {
  this: dcterms:created "2014-10-02T12:38:23+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" .
}