@prefix this: <http://rdf.disgenet.org/resource/nanopub/NP865513.RA4LP5vNr86WJqF4KFH2aDZ0Oj30RtVMz7YM1JN_hEaoM> .
@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:NP865513.RA4LP5vNr86WJqF4KFH2aDZ0Oj30RtVMz7YM1JN_hEaoM130_head {
  this: np:hasAssertion dgn-np:NP865513.RA4LP5vNr86WJqF4KFH2aDZ0Oj30RtVMz7YM1JN_hEaoM130_assertion;
    np:hasProvenance dgn-np:NP865513.RA4LP5vNr86WJqF4KFH2aDZ0Oj30RtVMz7YM1JN_hEaoM130_provenance;
    np:hasPublicationInfo dgn-np:NP865513.RA4LP5vNr86WJqF4KFH2aDZ0Oj30RtVMz7YM1JN_hEaoM130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP865513.RA4LP5vNr86WJqF4KFH2aDZ0Oj30RtVMz7YM1JN_hEaoM130_assertion a np:Assertion .
  
  dgn-np:NP865513.RA4LP5vNr86WJqF4KFH2aDZ0Oj30RtVMz7YM1JN_hEaoM130_provenance a np:Provenance .
  
  dgn-np:NP865513.RA4LP5vNr86WJqF4KFH2aDZ0Oj30RtVMz7YM1JN_hEaoM130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP865513.RA4LP5vNr86WJqF4KFH2aDZ0Oj30RtVMz7YM1JN_hEaoM130_assertion {
  miriam-gene:6775 a ncit:C16612 .
  
  lld:C0004364 a ncit:C7057 .
  
  dgn-gda:DGN9a7ce46562a0c07cd363cbbd1b7a71ae sio:SIO_000628 miriam-gene:6775, lld:C0004364;
    a sio:SIO_001122 .
}

dgn-np:NP865513.RA4LP5vNr86WJqF4KFH2aDZ0Oj30RtVMz7YM1JN_hEaoM130_provenance {
  dgn-np:NP865513.RA4LP5vNr86WJqF4KFH2aDZ0Oj30RtVMz7YM1JN_hEaoM130_assertion dcterms:description
      "[Taking into consideration that the different autoimmune diseases may share some common pathogenetic pathways, the aim of the present study was to evaluate the role of STAT4 rs7574865 polymorphism on acute allograft rejection.]. 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:21237270;
    prov:wasDerivedFrom dgn-void:befree-2016;
    prov:wasGeneratedBy eco:ECO_0000203 .
  
  dgn-void:befree-2016 pav:importedOn "2016-02-19"^^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:NP865513.RA4LP5vNr86WJqF4KFH2aDZ0Oj30RtVMz7YM1JN_hEaoM130_publicationInfo {
  this: dcterms:created "2016-05-13T12:48:17+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" .
}