@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP223110.RAeazE0CYWPaiyEwB-5kO1GYBWu9T6QEtTVtqmm-M8pwQ> .
@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:NP223110.RAeazE0CYWPaiyEwB-5kO1GYBWu9T6QEtTVtqmm-M8pwQ130_head {
  this: np:hasAssertion dgn-np:NP223110.RAeazE0CYWPaiyEwB-5kO1GYBWu9T6QEtTVtqmm-M8pwQ130_assertion;
    np:hasProvenance dgn-np:NP223110.RAeazE0CYWPaiyEwB-5kO1GYBWu9T6QEtTVtqmm-M8pwQ130_provenance;
    np:hasPublicationInfo dgn-np:NP223110.RAeazE0CYWPaiyEwB-5kO1GYBWu9T6QEtTVtqmm-M8pwQ130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP223110.RAeazE0CYWPaiyEwB-5kO1GYBWu9T6QEtTVtqmm-M8pwQ130_assertion a np:Assertion .
  
  dgn-np:NP223110.RAeazE0CYWPaiyEwB-5kO1GYBWu9T6QEtTVtqmm-M8pwQ130_provenance a np:Provenance .
  
  dgn-np:NP223110.RAeazE0CYWPaiyEwB-5kO1GYBWu9T6QEtTVtqmm-M8pwQ130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP223110.RAeazE0CYWPaiyEwB-5kO1GYBWu9T6QEtTVtqmm-M8pwQ130_assertion {
  miriam-gene:26191 a ncit:C16612 .
  
  lld:C0004364 a ncit:C7057 .
  
  dgn-gda:DGN8eecfbf10564fa3c190f0adabc93f16e sio:SIO_000628 miriam-gene:26191, lld:C0004364;
    a sio:SIO_001121 .
}

dgn-np:NP223110.RAeazE0CYWPaiyEwB-5kO1GYBWu9T6QEtTVtqmm-M8pwQ130_provenance {
  dgn-np:NP223110.RAeazE0CYWPaiyEwB-5kO1GYBWu9T6QEtTVtqmm-M8pwQ130_assertion dcterms:description
      "[The investigated PTPN22 gene polymorphisms (rs2488457, rs1310182 and rs3789604) were not associated with ocular Behcet's disease in two Chinese Han populations, and showed that it may be different from other classical autoimmune diseases.]. 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:22396730;
    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:NP223110.RAeazE0CYWPaiyEwB-5kO1GYBWu9T6QEtTVtqmm-M8pwQ130_publicationInfo {
  this: dcterms:created "2014-10-02T12:34:03+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" .
}