@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP522920.RAagjJu3og_9655-U4UmxE6aObFwnqjazrprFs7wtob5Y> .
@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:NP522920.RAagjJu3og_9655-U4UmxE6aObFwnqjazrprFs7wtob5Y130_head {
  this: np:hasAssertion dgn-np:NP522920.RAagjJu3og_9655-U4UmxE6aObFwnqjazrprFs7wtob5Y130_assertion;
    np:hasProvenance dgn-np:NP522920.RAagjJu3og_9655-U4UmxE6aObFwnqjazrprFs7wtob5Y130_provenance;
    np:hasPublicationInfo dgn-np:NP522920.RAagjJu3og_9655-U4UmxE6aObFwnqjazrprFs7wtob5Y130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP522920.RAagjJu3og_9655-U4UmxE6aObFwnqjazrprFs7wtob5Y130_assertion a np:Assertion .
  
  dgn-np:NP522920.RAagjJu3og_9655-U4UmxE6aObFwnqjazrprFs7wtob5Y130_provenance a np:Provenance .
  
  dgn-np:NP522920.RAagjJu3og_9655-U4UmxE6aObFwnqjazrprFs7wtob5Y130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP522920.RAagjJu3og_9655-U4UmxE6aObFwnqjazrprFs7wtob5Y130_assertion {
  miriam-gene:140805 a ncit:C16612 .
  
  lld:C0027697 a ncit:C7057 .
  
  dgn-gda:DGNa195a504e19a070e96be57690c89dbc9 sio:SIO_000628 miriam-gene:140805, lld:C0027697;
    a sio:SIO_001121 .
}

dgn-np:NP522920.RAagjJu3og_9655-U4UmxE6aObFwnqjazrprFs7wtob5Y130_provenance {
  dgn-np:NP522920.RAagjJu3og_9655-U4UmxE6aObFwnqjazrprFs7wtob5Y130_assertion dcterms:description
      "[These diseases include multiple sclerosis, rheumatoid arthritis, systemic lupus erythematosus, insulin-dependent diabetes mellitus, Crohn's disease, coeliac disease, Graves' disease, atrophic thyroiditis, Hashimoto's thyroiditis, myasthenia gravis, chronic active hepatitis, alopecia areata, uveitis, vitiligo, Turner's syndrome, glomerular nephritis, Berger's disease and idiopathic dilated cardiomyopathy.]. 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:1624073;
    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:NP522920.RAagjJu3og_9655-U4UmxE6aObFwnqjazrprFs7wtob5Y130_publicationInfo {
  this: dcterms:created "2014-10-02T12:37:11+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" .
}