@prefix this: <http://rdf.disgenet.org/resource/nanopub/NP74495.RA1rvWuwguA1_vRA2nHIlMygkVa69TMlWeUBUB4MnO8Yg> .
@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:NP74495.RA1rvWuwguA1_vRA2nHIlMygkVa69TMlWeUBUB4MnO8Yg130_head {
  this: np:hasAssertion dgn-np:NP74495.RA1rvWuwguA1_vRA2nHIlMygkVa69TMlWeUBUB4MnO8Yg130_assertion ;
    np:hasProvenance dgn-np:NP74495.RA1rvWuwguA1_vRA2nHIlMygkVa69TMlWeUBUB4MnO8Yg130_provenance ;
    np:hasPublicationInfo dgn-np:NP74495.RA1rvWuwguA1_vRA2nHIlMygkVa69TMlWeUBUB4MnO8Yg130_publicationInfo ;
    a np:Nanopublication .
  dgn-np:NP74495.RA1rvWuwguA1_vRA2nHIlMygkVa69TMlWeUBUB4MnO8Yg130_assertion a np:Assertion .
  dgn-np:NP74495.RA1rvWuwguA1_vRA2nHIlMygkVa69TMlWeUBUB4MnO8Yg130_provenance a np:Provenance .
  dgn-np:NP74495.RA1rvWuwguA1_vRA2nHIlMygkVa69TMlWeUBUB4MnO8Yg130_publicationInfo a np:PublicationInfo .
}
dgn-np:NP74495.RA1rvWuwguA1_vRA2nHIlMygkVa69TMlWeUBUB4MnO8Yg130_assertion {
  miriam-gene:3805 a ncit:C16612 .
  lld:C0018133 a ncit:C7057 .
  dgn-gda:DGN72f6a32bf8c8583dd9450ab0180f12c6 sio:SIO_000628 miriam-gene:3805 , lld:C0018133 ;
    a sio:SIO_001122 .
}
dgn-np:NP74495.RA1rvWuwguA1_vRA2nHIlMygkVa69TMlWeUBUB4MnO8Yg130_provenance {
  dgn-np:NP74495.RA1rvWuwguA1_vRA2nHIlMygkVa69TMlWeUBUB4MnO8Yg130_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:NP74495.RA1rvWuwguA1_vRA2nHIlMygkVa69TMlWeUBUB4MnO8Yg130_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 ;
    prv:usedData dgn-void:disgenetv3.0rdf ;
    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 "v4.0.0.0" .
  dgn-void:disgenetv3.0rdf pav:version "v4.0.0" .
}