@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP934316.RAYw1xQnQA7WsA4eGi2MbYXt47idRu1hpOXGEodq3Wxt4> .
@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:NP934316.RAYw1xQnQA7WsA4eGi2MbYXt47idRu1hpOXGEodq3Wxt4130_head {
  this: np:hasAssertion dgn-np:NP934316.RAYw1xQnQA7WsA4eGi2MbYXt47idRu1hpOXGEodq3Wxt4130_assertion;
    np:hasProvenance dgn-np:NP934316.RAYw1xQnQA7WsA4eGi2MbYXt47idRu1hpOXGEodq3Wxt4130_provenance;
    np:hasPublicationInfo dgn-np:NP934316.RAYw1xQnQA7WsA4eGi2MbYXt47idRu1hpOXGEodq3Wxt4130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP934316.RAYw1xQnQA7WsA4eGi2MbYXt47idRu1hpOXGEodq3Wxt4130_assertion a np:Assertion .
  
  dgn-np:NP934316.RAYw1xQnQA7WsA4eGi2MbYXt47idRu1hpOXGEodq3Wxt4130_provenance a np:Provenance .
  
  dgn-np:NP934316.RAYw1xQnQA7WsA4eGi2MbYXt47idRu1hpOXGEodq3Wxt4130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP934316.RAYw1xQnQA7WsA4eGi2MbYXt47idRu1hpOXGEodq3Wxt4130_assertion {
  miriam-gene:4599 a ncit:C16612 .
  
  lld:C0002171 a ncit:C7057 .
  
  dgn-gda:DGN9502c586c73e0291f4c7e117b33d9c5e sio:SIO_000628 miriam-gene:4599, lld:C0002171;
    a sio:SIO_001121 .
}

dgn-np:NP934316.RAYw1xQnQA7WsA4eGi2MbYXt47idRu1hpOXGEodq3Wxt4130_provenance {
  dgn-np:NP934316.RAYw1xQnQA7WsA4eGi2MbYXt47idRu1hpOXGEodq3Wxt4130_assertion dcterms:description
      "[Finally, the association of alopecia areata with Down's syndrome, the high frequency of alopecia areata in autoimmune polyglandular syndrome type I due to mutations of the autoimmune regulator (AIRE) gene on chromosome 21q22.3 and the finding of association with MX1, another gene in the Down's syndrome region of chromosome 21 indicate this area of the genome as a promising target for future-family based investigations.]. 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:12190641;
    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:NP934316.RAYw1xQnQA7WsA4eGi2MbYXt47idRu1hpOXGEodq3Wxt4130_publicationInfo {
  this: dcterms:created "2014-10-02T12:41:32+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" .
}