@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP259050.RAeKN1z7ioIBD-NxN3-Wz7sqbGpbIytGa3NebibCX2WKE> .
@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:NP259050.RAeKN1z7ioIBD-NxN3-Wz7sqbGpbIytGa3NebibCX2WKE130_head {
  this: np:hasAssertion dgn-np:NP259050.RAeKN1z7ioIBD-NxN3-Wz7sqbGpbIytGa3NebibCX2WKE130_assertion;
    np:hasProvenance dgn-np:NP259050.RAeKN1z7ioIBD-NxN3-Wz7sqbGpbIytGa3NebibCX2WKE130_provenance;
    np:hasPublicationInfo dgn-np:NP259050.RAeKN1z7ioIBD-NxN3-Wz7sqbGpbIytGa3NebibCX2WKE130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP259050.RAeKN1z7ioIBD-NxN3-Wz7sqbGpbIytGa3NebibCX2WKE130_assertion a np:Assertion .
  
  dgn-np:NP259050.RAeKN1z7ioIBD-NxN3-Wz7sqbGpbIytGa3NebibCX2WKE130_provenance a np:Provenance .
  
  dgn-np:NP259050.RAeKN1z7ioIBD-NxN3-Wz7sqbGpbIytGa3NebibCX2WKE130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP259050.RAeKN1z7ioIBD-NxN3-Wz7sqbGpbIytGa3NebibCX2WKE130_assertion {
  miriam-gene:3811 a ncit:C16612 .
  
  lld:C3463824 a ncit:C7057 .
  
  dgn-gda:DGNc5e1c692f0b2be5fedd3e40af6347008 sio:SIO_000628 miriam-gene:3811, lld:C3463824;
    a sio:SIO_001121 .
}

dgn-np:NP259050.RAeKN1z7ioIBD-NxN3-Wz7sqbGpbIytGa3NebibCX2WKE130_provenance {
  dgn-np:NP259050.RAeKN1z7ioIBD-NxN3-Wz7sqbGpbIytGa3NebibCX2WKE130_assertion dcterms:description
      "[In 178 patients receiving T-cell-depleted HLA-identical sibling transplants for acute myelogenous leukemia (AML), chronic myelogenous leukemia (CML), acute lymphoblastic leukemia (ALL), or myelodysplastic syndrome (MDS), analysis of donor KIR genotype with HLA genotype demonstrated that 62.9% of the patients lacked an HLA ligand for donor-inhibitory KIR.]. 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:15731175;
    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:NP259050.RAeKN1z7ioIBD-NxN3-Wz7sqbGpbIytGa3NebibCX2WKE130_publicationInfo {
  this: dcterms:created "2014-10-02T12:34:24+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" .
}