@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP593010.RACks8n1V-14zeO7LtkNelbt0pNoGLgiTzneRFN4gxr20> .
@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:NP593010.RACks8n1V-14zeO7LtkNelbt0pNoGLgiTzneRFN4gxr20130_head {
  this: np:hasAssertion dgn-np:NP593010.RACks8n1V-14zeO7LtkNelbt0pNoGLgiTzneRFN4gxr20130_assertion;
    np:hasProvenance dgn-np:NP593010.RACks8n1V-14zeO7LtkNelbt0pNoGLgiTzneRFN4gxr20130_provenance;
    np:hasPublicationInfo dgn-np:NP593010.RACks8n1V-14zeO7LtkNelbt0pNoGLgiTzneRFN4gxr20130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP593010.RACks8n1V-14zeO7LtkNelbt0pNoGLgiTzneRFN4gxr20130_assertion a np:Assertion .
  
  dgn-np:NP593010.RACks8n1V-14zeO7LtkNelbt0pNoGLgiTzneRFN4gxr20130_provenance a np:Provenance .
  
  dgn-np:NP593010.RACks8n1V-14zeO7LtkNelbt0pNoGLgiTzneRFN4gxr20130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP593010.RACks8n1V-14zeO7LtkNelbt0pNoGLgiTzneRFN4gxr20130_assertion {
  miriam-gene:326 a ncit:C16612 .
  
  lld:C0040128 a ncit:C7057 .
  
  dgn-gda:DGN4d75258d85669c453d67b13876873552 sio:SIO_000628 miriam-gene:326, lld:C0040128;
    a sio:SIO_001121 .
}

dgn-np:NP593010.RACks8n1V-14zeO7LtkNelbt0pNoGLgiTzneRFN4gxr20130_provenance {
  dgn-np:NP593010.RACks8n1V-14zeO7LtkNelbt0pNoGLgiTzneRFN4gxr20130_assertion dcterms:description
      "[Type 1 diabetes, alopecia, vitiligo, ectodermal dystrophy, celiac disease and other intestinal dysfunctions, chronic atrophic gastritis, chronic active hepatitis, autoimmune thyroid disorders, pernicious anemia and premature ovarian failure are other rare associated diseases although other conditions have been associated with APECED.]. 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:23000069;
    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:NP593010.RACks8n1V-14zeO7LtkNelbt0pNoGLgiTzneRFN4gxr20130_publicationInfo {
  this: dcterms:created "2014-10-02T12:37:56+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" .
}