@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP865813.RAreUNG-htYtYhlXxIilzBzVn16goKkUJO1GAvQTFaWkA> .
@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:NP865813.RAreUNG-htYtYhlXxIilzBzVn16goKkUJO1GAvQTFaWkA130_head {
  this: np:hasAssertion dgn-np:NP865813.RAreUNG-htYtYhlXxIilzBzVn16goKkUJO1GAvQTFaWkA130_assertion ;
    np:hasProvenance dgn-np:NP865813.RAreUNG-htYtYhlXxIilzBzVn16goKkUJO1GAvQTFaWkA130_provenance ;
    np:hasPublicationInfo dgn-np:NP865813.RAreUNG-htYtYhlXxIilzBzVn16goKkUJO1GAvQTFaWkA130_publicationInfo ;
    a np:Nanopublication .
  dgn-np:NP865813.RAreUNG-htYtYhlXxIilzBzVn16goKkUJO1GAvQTFaWkA130_assertion a np:Assertion .
  dgn-np:NP865813.RAreUNG-htYtYhlXxIilzBzVn16goKkUJO1GAvQTFaWkA130_provenance a np:Provenance .
  dgn-np:NP865813.RAreUNG-htYtYhlXxIilzBzVn16goKkUJO1GAvQTFaWkA130_publicationInfo a np:PublicationInfo .
}
dgn-np:NP865813.RAreUNG-htYtYhlXxIilzBzVn16goKkUJO1GAvQTFaWkA130_assertion {
  miriam-gene:3133 a ncit:C16612 .
  lld:C0920028 a ncit:C7057 .
  dgn-gda:DGNdbd49c363afb408854d77765ea7909d3 sio:SIO_000628 miriam-gene:3133 , lld:C0920028 ;
    a sio:SIO_001121 .
}
dgn-np:NP865813.RAreUNG-htYtYhlXxIilzBzVn16goKkUJO1GAvQTFaWkA130_provenance {
  dgn-np:NP865813.RAreUNG-htYtYhlXxIilzBzVn16goKkUJO1GAvQTFaWkA130_assertion dcterms:description "[In order to determine whether matching/mismatching for microsatellite polymorphism provides useful information on acute graft-vs-host disease (GVHD), survival, and leukemia relapse in hematopoietic stem cell (HSC) transplantation, we genotyped for polymorphisms at 13 microsatellite loci within the major histocompatibility complex (MHC) of 100 unrelated HSC transplant donor-recipient pairs who were matched at five classical human leukocyte antigen (HLA) loci.]. 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:15009808 ;
    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:NP865813.RAreUNG-htYtYhlXxIilzBzVn16goKkUJO1GAvQTFaWkA130_publicationInfo {
  this: dcterms:created "2014-10-02T12:40:49+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" .
}