@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP262237.RAy9VJ3acDFZyEGB1KPGXn5DrqMzqDyEm-n5BsXcjSmrQ> .
@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:NP262237.RAy9VJ3acDFZyEGB1KPGXn5DrqMzqDyEm-n5BsXcjSmrQ130_head {
  this: np:hasAssertion dgn-np:NP262237.RAy9VJ3acDFZyEGB1KPGXn5DrqMzqDyEm-n5BsXcjSmrQ130_assertion;
    np:hasProvenance dgn-np:NP262237.RAy9VJ3acDFZyEGB1KPGXn5DrqMzqDyEm-n5BsXcjSmrQ130_provenance;
    np:hasPublicationInfo dgn-np:NP262237.RAy9VJ3acDFZyEGB1KPGXn5DrqMzqDyEm-n5BsXcjSmrQ130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP262237.RAy9VJ3acDFZyEGB1KPGXn5DrqMzqDyEm-n5BsXcjSmrQ130_assertion a np:Assertion .
  
  dgn-np:NP262237.RAy9VJ3acDFZyEGB1KPGXn5DrqMzqDyEm-n5BsXcjSmrQ130_provenance a np:Provenance .
  
  dgn-np:NP262237.RAy9VJ3acDFZyEGB1KPGXn5DrqMzqDyEm-n5BsXcjSmrQ130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP262237.RAy9VJ3acDFZyEGB1KPGXn5DrqMzqDyEm-n5BsXcjSmrQ130_assertion {
  miriam-gene:23274 a ncit:C16612 .
  
  lld:C0266273 a ncit:C7057 .
  
  dgn-gda:DGN40b3e3f52b25e078398f6cb4e5efb257 sio:SIO_000628 miriam-gene:23274, lld:C0266273;
    a sio:SIO_001121 .
}

dgn-np:NP262237.RAy9VJ3acDFZyEGB1KPGXn5DrqMzqDyEm-n5BsXcjSmrQ130_provenance {
  dgn-np:NP262237.RAy9VJ3acDFZyEGB1KPGXn5DrqMzqDyEm-n5BsXcjSmrQ130_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:NP262237.RAy9VJ3acDFZyEGB1KPGXn5DrqMzqDyEm-n5BsXcjSmrQ130_publicationInfo {
  this: dcterms:created "2014-10-02T12:34:26+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" .
}