@prefix this: <http://rdf.disgenet.org/resource/nanopub/NP365279.RAlXFjhhz1hLMi366JnWXrO9KnEmFg4cp1LHd69Qda7bU> .
@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/> .
@prefix wi: <http://purl.org/ontology/wi/core#> .
@prefix prov: <http://www.w3.org/ns/prov#> .
@prefix pav: <http://purl.org/pav/> .
@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/resource/nanopub/> .
@prefix dgn-gda: <http://rdf.disgenet.org/resource/gda/> .
@prefix dgn-void: <http://rdf.disgenet.org/v4.0.0/void/> .
dgn-np:NP365279.RAlXFjhhz1hLMi366JnWXrO9KnEmFg4cp1LHd69Qda7bU130_head {
  this: np:hasAssertion dgn-np:NP365279.RAlXFjhhz1hLMi366JnWXrO9KnEmFg4cp1LHd69Qda7bU130_assertion ;
    np:hasProvenance dgn-np:NP365279.RAlXFjhhz1hLMi366JnWXrO9KnEmFg4cp1LHd69Qda7bU130_provenance ;
    np:hasPublicationInfo dgn-np:NP365279.RAlXFjhhz1hLMi366JnWXrO9KnEmFg4cp1LHd69Qda7bU130_publicationInfo ;
    a np:Nanopublication .
  dgn-np:NP365279.RAlXFjhhz1hLMi366JnWXrO9KnEmFg4cp1LHd69Qda7bU130_assertion a np:Assertion .
  dgn-np:NP365279.RAlXFjhhz1hLMi366JnWXrO9KnEmFg4cp1LHd69Qda7bU130_provenance a np:Provenance .
  dgn-np:NP365279.RAlXFjhhz1hLMi366JnWXrO9KnEmFg4cp1LHd69Qda7bU130_publicationInfo a np:PublicationInfo .
}
dgn-np:NP365279.RAlXFjhhz1hLMi366JnWXrO9KnEmFg4cp1LHd69Qda7bU130_assertion {
  miriam-gene:326 a ncit:C16612 .
  lld:C0085859 a ncit:C7057 .
  dgn-gda:DGN2b8cd42e7ac72070953f7b68ce0b04e7 sio:SIO_000628 miriam-gene:326 , lld:C0085859 ;
    a sio:SIO_001121 .
}
dgn-np:NP365279.RAlXFjhhz1hLMi366JnWXrO9KnEmFg4cp1LHd69Qda7bU130_provenance {
  dgn-np:NP365279.RAlXFjhhz1hLMi366JnWXrO9KnEmFg4cp1LHd69Qda7bU130_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-2016 ;
    prov:wasGeneratedBy eco:ECO_0000203 .
  dgn-void:befree-2016 pav:importedOn "2016-02-19"^^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:NP365279.RAlXFjhhz1hLMi366JnWXrO9KnEmFg4cp1LHd69Qda7bU130_publicationInfo {
  this: dcterms:created "2016-05-13T12:44:31+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:disgenetv3.0rdf ;
    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 "v4.0.0.0" .
  dgn-void:disgenetv3.0rdf pav:version "v4.0.0" .
}