@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP238575.RAyvF2hNbTJBUJuANblhqIRlPtGd8Ahsymb_T0fewXLcM> .
@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:NP238575.RAyvF2hNbTJBUJuANblhqIRlPtGd8Ahsymb_T0fewXLcM130_head {
  this: np:hasAssertion dgn-np:NP238575.RAyvF2hNbTJBUJuANblhqIRlPtGd8Ahsymb_T0fewXLcM130_assertion ;
    np:hasProvenance dgn-np:NP238575.RAyvF2hNbTJBUJuANblhqIRlPtGd8Ahsymb_T0fewXLcM130_provenance ;
    np:hasPublicationInfo dgn-np:NP238575.RAyvF2hNbTJBUJuANblhqIRlPtGd8Ahsymb_T0fewXLcM130_publicationInfo ;
    a np:Nanopublication .
  dgn-np:NP238575.RAyvF2hNbTJBUJuANblhqIRlPtGd8Ahsymb_T0fewXLcM130_assertion a np:Assertion .
  dgn-np:NP238575.RAyvF2hNbTJBUJuANblhqIRlPtGd8Ahsymb_T0fewXLcM130_provenance a np:Provenance .
  dgn-np:NP238575.RAyvF2hNbTJBUJuANblhqIRlPtGd8Ahsymb_T0fewXLcM130_publicationInfo a np:PublicationInfo .
}
dgn-np:NP238575.RAyvF2hNbTJBUJuANblhqIRlPtGd8Ahsymb_T0fewXLcM130_assertion {
  miriam-gene:3577 a ncit:C16612 .
  lld:C0011847 a ncit:C7057 .
  dgn-gda:DGNa11e52f29ebd60c2dc8b21cfd3691944 sio:SIO_000628 miriam-gene:3577 , lld:C0011847 ;
    a sio:SIO_001121 .
}
dgn-np:NP238575.RAyvF2hNbTJBUJuANblhqIRlPtGd8Ahsymb_T0fewXLcM130_provenance {
  dgn-np:NP238575.RAyvF2hNbTJBUJuANblhqIRlPtGd8Ahsymb_T0fewXLcM130_assertion dcterms:description "[The donor GA/AA genotypes of CXCR1 -2668G/A (rs2671222) were associated with increased risk for acute rejection even after adjusting for covariates such as gender, diabetes, preemptive transplantation, immunosuppressive regimen, relationship with the donor, and human leukocyte antigen mismatch (adjusted odds ratio 3.56; 95% confidence interval 1.37-9.27; P=0.009).]. 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:21452410 ;
    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:NP238575.RAyvF2hNbTJBUJuANblhqIRlPtGd8Ahsymb_T0fewXLcM130_publicationInfo {
  this: dcterms:created "2014-10-02T12:34:13+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" .
}