@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP58268.RAfave8pZMb3YMRZv85bpZiKdYB7x-uMW2pbxR-QdkcGw> .
@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:NP58268.RAfave8pZMb3YMRZv85bpZiKdYB7x-uMW2pbxR-QdkcGw130_head {
  this: np:hasAssertion dgn-np:NP58268.RAfave8pZMb3YMRZv85bpZiKdYB7x-uMW2pbxR-QdkcGw130_assertion;
    np:hasProvenance dgn-np:NP58268.RAfave8pZMb3YMRZv85bpZiKdYB7x-uMW2pbxR-QdkcGw130_provenance;
    np:hasPublicationInfo dgn-np:NP58268.RAfave8pZMb3YMRZv85bpZiKdYB7x-uMW2pbxR-QdkcGw130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP58268.RAfave8pZMb3YMRZv85bpZiKdYB7x-uMW2pbxR-QdkcGw130_assertion a np:Assertion .
  
  dgn-np:NP58268.RAfave8pZMb3YMRZv85bpZiKdYB7x-uMW2pbxR-QdkcGw130_provenance a np:Provenance .
  
  dgn-np:NP58268.RAfave8pZMb3YMRZv85bpZiKdYB7x-uMW2pbxR-QdkcGw130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP58268.RAfave8pZMb3YMRZv85bpZiKdYB7x-uMW2pbxR-QdkcGw130_assertion {
  miriam-gene:3106 a ncit:C16612 .
  
  lld:C0018133 a ncit:C7057 .
  
  dgn-gda:DGNc0f89e6f37fe45f1b64170dd9984b0be sio:SIO_000628 miriam-gene:3106, lld:C0018133;
    a sio:SIO_001122 .
}

dgn-np:NP58268.RAfave8pZMb3YMRZv85bpZiKdYB7x-uMW2pbxR-QdkcGw130_provenance {
  dgn-np:NP58268.RAfave8pZMb3YMRZv85bpZiKdYB7x-uMW2pbxR-QdkcGw130_assertion dcterms:description
      "[Overall, these results suggest that the matching of microsatellite polymorphisms within the HLA region, especially the ones farthest from the classical HLA loci, was not useful indicator for the outcome of HSC transplantation from unrelated donors. In this regard, the future determination of the genome-wide microsatellite genotypes in HLA-matched donor-recipient pairs, outside the MHC, may be a better possibility for identifying minor histocompatibility genes in linkage disequilibria with microsatellites as potential predictive markers for the occurrence of acute GVHD and survival rate in HSC 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:15009808;
    prov:wasDerivedFrom dgn-void:gad-20130706;
    prov:wasGeneratedBy eco:ECO_0000203 .
  
  dgn-void:gad-20130706 pav:importedOn "2013-07-06"^^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:NP58268.RAfave8pZMb3YMRZv85bpZiKdYB7x-uMW2pbxR-QdkcGw130_publicationInfo {
  this: dcterms:created "2014-10-02T12:32:27+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" .
}