@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP507337.RAtpqyfDuCw5zP51wEzuZ5NZ-GjU8hX-4m6IGfMJbnH4A> .
@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:NP507337.RAtpqyfDuCw5zP51wEzuZ5NZ-GjU8hX-4m6IGfMJbnH4A130_head {
  this: np:hasAssertion dgn-np:NP507337.RAtpqyfDuCw5zP51wEzuZ5NZ-GjU8hX-4m6IGfMJbnH4A130_assertion;
    np:hasProvenance dgn-np:NP507337.RAtpqyfDuCw5zP51wEzuZ5NZ-GjU8hX-4m6IGfMJbnH4A130_provenance;
    np:hasPublicationInfo dgn-np:NP507337.RAtpqyfDuCw5zP51wEzuZ5NZ-GjU8hX-4m6IGfMJbnH4A130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP507337.RAtpqyfDuCw5zP51wEzuZ5NZ-GjU8hX-4m6IGfMJbnH4A130_assertion a np:Assertion .
  
  dgn-np:NP507337.RAtpqyfDuCw5zP51wEzuZ5NZ-GjU8hX-4m6IGfMJbnH4A130_provenance a np:Provenance .
  
  dgn-np:NP507337.RAtpqyfDuCw5zP51wEzuZ5NZ-GjU8hX-4m6IGfMJbnH4A130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP507337.RAtpqyfDuCw5zP51wEzuZ5NZ-GjU8hX-4m6IGfMJbnH4A130_assertion {
  miriam-gene:3595 a ncit:C16612 .
  
  lld:C0023348 a ncit:C7057 .
  
  dgn-gda:DGN5a5e667a00a68f135ca35ee343922267 sio:SIO_000628 miriam-gene:3595, lld:C0023348;
    a sio:SIO_001121 .
}

dgn-np:NP507337.RAtpqyfDuCw5zP51wEzuZ5NZ-GjU8hX-4m6IGfMJbnH4A130_provenance {
  dgn-np:NP507337.RAtpqyfDuCw5zP51wEzuZ5NZ-GjU8hX-4m6IGfMJbnH4A130_assertion dcterms:description
      "[Single nucleotide polymorphisms (SNPs) in the 5' flanking region of IL12RB2 are frequently detected in lepromatous leprosy patients, and may be possible immunogenetic factors that reduce transcriptional activity of the IL-12Rbeta2 gene in Jurkat T cells.]. 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:18771340;
    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:NP507337.RAtpqyfDuCw5zP51wEzuZ5NZ-GjU8hX-4m6IGfMJbnH4A130_publicationInfo {
  this: dcterms:created "2014-10-02T12:37:02+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" .
}