@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP828468.RA3YcaS4QCmmPCMsABl_3zGnKL_ie4S1vwt2TKT7QoSO4> .
@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:NP828468.RA3YcaS4QCmmPCMsABl_3zGnKL_ie4S1vwt2TKT7QoSO4130_head {
  this: np:hasAssertion dgn-np:NP828468.RA3YcaS4QCmmPCMsABl_3zGnKL_ie4S1vwt2TKT7QoSO4130_assertion;
    np:hasProvenance dgn-np:NP828468.RA3YcaS4QCmmPCMsABl_3zGnKL_ie4S1vwt2TKT7QoSO4130_provenance;
    np:hasPublicationInfo dgn-np:NP828468.RA3YcaS4QCmmPCMsABl_3zGnKL_ie4S1vwt2TKT7QoSO4130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP828468.RA3YcaS4QCmmPCMsABl_3zGnKL_ie4S1vwt2TKT7QoSO4130_assertion a np:Assertion .
  
  dgn-np:NP828468.RA3YcaS4QCmmPCMsABl_3zGnKL_ie4S1vwt2TKT7QoSO4130_provenance a np:Provenance .
  
  dgn-np:NP828468.RA3YcaS4QCmmPCMsABl_3zGnKL_ie4S1vwt2TKT7QoSO4130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP828468.RA3YcaS4QCmmPCMsABl_3zGnKL_ie4S1vwt2TKT7QoSO4130_assertion {
  miriam-gene:3595 a ncit:C16612 .
  
  lld:C0031099 a ncit:C7057 .
  
  dgn-gda:DGN74bdff137420b0dd5d880cecbe8b8d7a sio:SIO_000628 miriam-gene:3595, lld:C0031099;
    a sio:SIO_001121 .
}

dgn-np:NP828468.RA3YcaS4QCmmPCMsABl_3zGnKL_ie4S1vwt2TKT7QoSO4130_provenance {
  dgn-np:NP828468.RA3YcaS4QCmmPCMsABl_3zGnKL_ie4S1vwt2TKT7QoSO4130_assertion dcterms:description
      "[To elucidate the role of the cell-mediated immune (CMI) response in the pathogenesis of periodontitis, Japanese periodontal patients were subjected to single nucleotide polymorphism (SNP) analyses of the 5' flanking region of IL12RB2, whose variants are frequently detected in lepromatous leprosy patients, in which the very weak cellular immune response is caused by low expression of IL-12Rbeta2.]. 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:18353079;
    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:NP828468.RA3YcaS4QCmmPCMsABl_3zGnKL_ie4S1vwt2TKT7QoSO4130_publicationInfo {
  this: dcterms:created "2014-10-02T12:40:27+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" .
}