@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP645178.RAaiNzdeSwoXr0c0EyFGMWce8GH2lJq0h5WTaVbDuCAYo> .
@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:NP645178.RAaiNzdeSwoXr0c0EyFGMWce8GH2lJq0h5WTaVbDuCAYo130_head {
  this: np:hasAssertion dgn-np:NP645178.RAaiNzdeSwoXr0c0EyFGMWce8GH2lJq0h5WTaVbDuCAYo130_assertion;
    np:hasProvenance dgn-np:NP645178.RAaiNzdeSwoXr0c0EyFGMWce8GH2lJq0h5WTaVbDuCAYo130_provenance;
    np:hasPublicationInfo dgn-np:NP645178.RAaiNzdeSwoXr0c0EyFGMWce8GH2lJq0h5WTaVbDuCAYo130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP645178.RAaiNzdeSwoXr0c0EyFGMWce8GH2lJq0h5WTaVbDuCAYo130_assertion a np:Assertion .
  
  dgn-np:NP645178.RAaiNzdeSwoXr0c0EyFGMWce8GH2lJq0h5WTaVbDuCAYo130_provenance a np:Provenance .
  
  dgn-np:NP645178.RAaiNzdeSwoXr0c0EyFGMWce8GH2lJq0h5WTaVbDuCAYo130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP645178.RAaiNzdeSwoXr0c0EyFGMWce8GH2lJq0h5WTaVbDuCAYo130_assertion {
  miriam-gene:4261 a ncit:C16612 .
  
  lld:C0266273 a ncit:C7057 .
  
  dgn-gda:DGN31e2b8c8d9d9cb5a02f9f9cb5b33cbe1 sio:SIO_000628 miriam-gene:4261, lld:C0266273;
    a sio:SIO_001121 .
}

dgn-np:NP645178.RAaiNzdeSwoXr0c0EyFGMWce8GH2lJq0h5WTaVbDuCAYo130_provenance {
  dgn-np:NP645178.RAaiNzdeSwoXr0c0EyFGMWce8GH2lJq0h5WTaVbDuCAYo130_assertion dcterms:description
      "[Two alleles at 16p13 are independently associated with the risk of Addison's disease in the Norwegian population, suggesting this chromosomal region to harbor common autoimmunity gene(s), CLEC16A and CIITA being possible independent candidates.]. 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:18593762;
    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:NP645178.RAaiNzdeSwoXr0c0EyFGMWce8GH2lJq0h5WTaVbDuCAYo130_publicationInfo {
  this: dcterms:created "2014-10-02T12:38:28+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" .
}