@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP95784.RADj09VPNJrWmQNqb-t8-G6v_p_tJCg5mNX-nJLYlWyCM> .
@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:NP95784.RADj09VPNJrWmQNqb-t8-G6v_p_tJCg5mNX-nJLYlWyCM130_head {
  this: np:hasAssertion dgn-np:NP95784.RADj09VPNJrWmQNqb-t8-G6v_p_tJCg5mNX-nJLYlWyCM130_assertion;
    np:hasProvenance dgn-np:NP95784.RADj09VPNJrWmQNqb-t8-G6v_p_tJCg5mNX-nJLYlWyCM130_provenance;
    np:hasPublicationInfo dgn-np:NP95784.RADj09VPNJrWmQNqb-t8-G6v_p_tJCg5mNX-nJLYlWyCM130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP95784.RADj09VPNJrWmQNqb-t8-G6v_p_tJCg5mNX-nJLYlWyCM130_assertion a np:Assertion .
  
  dgn-np:NP95784.RADj09VPNJrWmQNqb-t8-G6v_p_tJCg5mNX-nJLYlWyCM130_provenance a np:Provenance .
  
  dgn-np:NP95784.RADj09VPNJrWmQNqb-t8-G6v_p_tJCg5mNX-nJLYlWyCM130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP95784.RADj09VPNJrWmQNqb-t8-G6v_p_tJCg5mNX-nJLYlWyCM130_assertion {
  miriam-gene:22925 a ncit:C16612 .
  
  lld:C0017665 a ncit:C7057 .
  
  dgn-gda:DGN18aac82b2c11973582814ccb8e29d219 sio:SIO_000628 miriam-gene:22925, lld:C0017665;
    a sio:SIO_001122 .
}

dgn-np:NP95784.RADj09VPNJrWmQNqb-t8-G6v_p_tJCg5mNX-nJLYlWyCM130_provenance {
  dgn-np:NP95784.RADj09VPNJrWmQNqb-t8-G6v_p_tJCg5mNX-nJLYlWyCM130_assertion dcterms:description
      "[An HLA-DQA1 allele on chromosome 6p21 is most closely associated with idiopathic membranous nephropathy in persons of white ancestry. This allele may facilitate an autoimmune response against targets such as variants of PLA2R1. Our findings suggest a basis for understanding this disease and illuminate how adaptive immunity is regulated by HLA.]. 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:21323541;
    prov:wasDerivedFrom dgn-void:gad-20130706;
    prov:wasGeneratedBy eco:ECO_0000203 .
  
  dgn-void:gad-20130706 pav:importedOn "2013-07-06"^^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:NP95784.RADj09VPNJrWmQNqb-t8-G6v_p_tJCg5mNX-nJLYlWyCM130_publicationInfo {
  this: dcterms:created "2014-10-02T12:32:47+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" .
}