@prefix this: <http://rdf.disgenet.org/resource/nanopub/NP74488.RAtaHmgBZ5HJoZN61yKU1EScIyQiiNQvuemK6sQ0ZZEDs> .
@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/> .
@prefix wi: <http://purl.org/ontology/wi/core#> .
@prefix prov: <http://www.w3.org/ns/prov#> .
@prefix pav: <http://purl.org/pav/> .
@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/resource/nanopub/> .
@prefix dgn-gda: <http://rdf.disgenet.org/resource/gda/> .
@prefix dgn-void: <http://rdf.disgenet.org/v4.0.0/void/> .
dgn-np:NP74488.RAtaHmgBZ5HJoZN61yKU1EScIyQiiNQvuemK6sQ0ZZEDs130_head {
  this: np:hasAssertion dgn-np:NP74488.RAtaHmgBZ5HJoZN61yKU1EScIyQiiNQvuemK6sQ0ZZEDs130_assertion ;
    np:hasProvenance dgn-np:NP74488.RAtaHmgBZ5HJoZN61yKU1EScIyQiiNQvuemK6sQ0ZZEDs130_provenance ;
    np:hasPublicationInfo dgn-np:NP74488.RAtaHmgBZ5HJoZN61yKU1EScIyQiiNQvuemK6sQ0ZZEDs130_publicationInfo ;
    a np:Nanopublication .
  dgn-np:NP74488.RAtaHmgBZ5HJoZN61yKU1EScIyQiiNQvuemK6sQ0ZZEDs130_assertion a np:Assertion .
  dgn-np:NP74488.RAtaHmgBZ5HJoZN61yKU1EScIyQiiNQvuemK6sQ0ZZEDs130_provenance a np:Provenance .
  dgn-np:NP74488.RAtaHmgBZ5HJoZN61yKU1EScIyQiiNQvuemK6sQ0ZZEDs130_publicationInfo a np:PublicationInfo .
}
dgn-np:NP74488.RAtaHmgBZ5HJoZN61yKU1EScIyQiiNQvuemK6sQ0ZZEDs130_assertion {
  miriam-gene:3808 a ncit:C16612 .
  lld:C0018133 a ncit:C7057 .
  dgn-gda:DGN5be90680c86ea385ea4a281b252ab6d3 sio:SIO_000628 miriam-gene:3808 , lld:C0018133 ;
    a sio:SIO_001122 .
}
dgn-np:NP74488.RAtaHmgBZ5HJoZN61yKU1EScIyQiiNQvuemK6sQ0ZZEDs130_provenance {
  dgn-np:NP74488.RAtaHmgBZ5HJoZN61yKU1EScIyQiiNQvuemK6sQ0ZZEDs130_assertion dcterms:description "[In conclusion, our results reveal a great diversity for KIR genotypes in donors and recipients of BMT and that the risk of GVHD was maximum in unrelated BMT when the recipient KIR genotype was included in the donor KIR genotype.]. 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:12039408 ;
    prov:wasDerivedFrom dgn-void:gad-20150221 ;
    prov:wasGeneratedBy eco:ECO_0000203 .
  dgn-void:gad-20150221 pav:importedOn "2015-02-21"^^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:NP74488.RAtaHmgBZ5HJoZN61yKU1EScIyQiiNQvuemK6sQ0ZZEDs130_publicationInfo {
  this: dcterms:created "2016-05-13T12:42:22+02:00"^^xsd:dateTime ;
    dcterms:rights <http://opendatacommons.org/licenses/odbl/1.0/> ;
    dcterms:rightsHolder dgn-void:IBIGroup ;
    dcterms:subject sio:SIO_000983 ;
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    pav:createdBy <http://orcid.org/0000-0003-0169-8159> ;
    pav:version "v4.0.0.0" .
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}