@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP216806.RA0glauviSFSEbpTm2psA1jJdFUSQq1r3S6rigA3eDauA> .
@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:NP216806.RA0glauviSFSEbpTm2psA1jJdFUSQq1r3S6rigA3eDauA130_head {
  this: np:hasAssertion dgn-np:NP216806.RA0glauviSFSEbpTm2psA1jJdFUSQq1r3S6rigA3eDauA130_assertion;
    np:hasProvenance dgn-np:NP216806.RA0glauviSFSEbpTm2psA1jJdFUSQq1r3S6rigA3eDauA130_provenance;
    np:hasPublicationInfo dgn-np:NP216806.RA0glauviSFSEbpTm2psA1jJdFUSQq1r3S6rigA3eDauA130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP216806.RA0glauviSFSEbpTm2psA1jJdFUSQq1r3S6rigA3eDauA130_assertion a np:Assertion .
  
  dgn-np:NP216806.RA0glauviSFSEbpTm2psA1jJdFUSQq1r3S6rigA3eDauA130_provenance a np:Provenance .
  
  dgn-np:NP216806.RA0glauviSFSEbpTm2psA1jJdFUSQq1r3S6rigA3eDauA130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP216806.RA0glauviSFSEbpTm2psA1jJdFUSQq1r3S6rigA3eDauA130_assertion {
  miriam-gene:3811 a ncit:C16612 .
  
  lld:C0018133 a ncit:C7057 .
  
  dgn-gda:DGN32f195d2786c543241f65638a136514d sio:SIO_000628 miriam-gene:3811, lld:C0018133;
    a sio:SIO_001121 .
}

dgn-np:NP216806.RA0glauviSFSEbpTm2psA1jJdFUSQq1r3S6rigA3eDauA130_provenance {
  dgn-np:NP216806.RA0glauviSFSEbpTm2psA1jJdFUSQq1r3S6rigA3eDauA130_assertion dcterms:description
      "[Our study suggests that KIR genotyping of donor and recipient pairs could contribute to the identification of patients at high risk for developing severe complications of haematopoietic SCT and thus may help with the choice of intensity of GVHD prophylaxis.]. 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:20173792;
    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:NP216806.RA0glauviSFSEbpTm2psA1jJdFUSQq1r3S6rigA3eDauA130_publicationInfo {
  this: dcterms:created "2014-10-02T12:34:00+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" .
}