@prefix dct: <http://purl.org/dc/terms/> .
@prefix orcid: <http://orcid.org/> .
@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP77919.RAx9Ilb1TOP7uBnoXCcXn2oAsxcH3FKRWqAPc5IXuZg2I> .
@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 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:NP77919.RAx9Ilb1TOP7uBnoXCcXn2oAsxcH3FKRWqAPc5IXuZg2I130_head {
  this: np:hasAssertion dgn-np:NP77919.RAx9Ilb1TOP7uBnoXCcXn2oAsxcH3FKRWqAPc5IXuZg2I130_assertion;
    np:hasProvenance dgn-np:NP77919.RAx9Ilb1TOP7uBnoXCcXn2oAsxcH3FKRWqAPc5IXuZg2I130_provenance;
    np:hasPublicationInfo dgn-np:NP77919.RAx9Ilb1TOP7uBnoXCcXn2oAsxcH3FKRWqAPc5IXuZg2I130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP77919.RAx9Ilb1TOP7uBnoXCcXn2oAsxcH3FKRWqAPc5IXuZg2I130_assertion a np:Assertion .
  
  dgn-np:NP77919.RAx9Ilb1TOP7uBnoXCcXn2oAsxcH3FKRWqAPc5IXuZg2I130_provenance a np:Provenance .
  
  dgn-np:NP77919.RAx9Ilb1TOP7uBnoXCcXn2oAsxcH3FKRWqAPc5IXuZg2I130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP77919.RAx9Ilb1TOP7uBnoXCcXn2oAsxcH3FKRWqAPc5IXuZg2I130_assertion {
  miriam-gene:149233 a ncit:C16612 .
  
  lld:C0021390 a ncit:C7057 .
  
  dgn-gda:DGN270a356797d3435544a6e94391d25b7e sio:SIO_000628 miriam-gene:149233, lld:C0021390;
    a sio:SIO_001122 .
}

dgn-np:NP77919.RAx9Ilb1TOP7uBnoXCcXn2oAsxcH3FKRWqAPc5IXuZg2I130_provenance {
  dgn-np:NP77919.RAx9Ilb1TOP7uBnoXCcXn2oAsxcH3FKRWqAPc5IXuZg2I130_assertion dct:description
      "[To replicate the association of IL23R R381Q (rs11209026) with inflammatory bowel disease (IBD), examine the effect of the two nonsynonymous variations, Q3H and L310P, on IBD, and to study gender distribution of these variants in IBD patients.]. 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:19294505;
    prov:wasDerivedFrom dgn-void:gad-20130706;
    prov:wasGeneratedBy eco:ECO_0000203 .
  
  dgn-void:gad-20130706 pav:importedOn "2013-07-06"^^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:NP77919.RAx9Ilb1TOP7uBnoXCcXn2oAsxcH3FKRWqAPc5IXuZg2I130_publicationInfo {
  this: dct:created "2014-10-02T12:32:38+02:00"^^xsd:dateTime;
    dct:rights <http://opendatacommons.org/licenses/odbl/1.0/>;
    dct:rightsHolder dgn-void:IBIGroup;
    dct:subject sio:SIO_000983;
    prv:usedData dgn-void:disgenetrdf;
    pav:authoredBy orcid:0000-0001-5999-6269, orcid:0000-0002-7534-7661, orcid:0000-0002-9383-528X,
      orcid:0000-0003-0169-8159, orcid:0000-0003-1244-7654;
    pav:createdBy orcid:0000-0003-0169-8159;
    pav:version "v2.1.0.0" .
  
  dgn-void:disgenetrdf pav:version "v2.1.0" .
}