@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP773566.RAcOtFqOH6tre6HiOOGsAnyW7GHINnP77EP8Sn-MPQ7GU> .
@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:NP773566.RAcOtFqOH6tre6HiOOGsAnyW7GHINnP77EP8Sn-MPQ7GU130_head {
  this: np:hasAssertion dgn-np:NP773566.RAcOtFqOH6tre6HiOOGsAnyW7GHINnP77EP8Sn-MPQ7GU130_assertion;
    np:hasProvenance dgn-np:NP773566.RAcOtFqOH6tre6HiOOGsAnyW7GHINnP77EP8Sn-MPQ7GU130_provenance;
    np:hasPublicationInfo dgn-np:NP773566.RAcOtFqOH6tre6HiOOGsAnyW7GHINnP77EP8Sn-MPQ7GU130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP773566.RAcOtFqOH6tre6HiOOGsAnyW7GHINnP77EP8Sn-MPQ7GU130_assertion a np:Assertion .
  
  dgn-np:NP773566.RAcOtFqOH6tre6HiOOGsAnyW7GHINnP77EP8Sn-MPQ7GU130_provenance a np:Provenance .
  
  dgn-np:NP773566.RAcOtFqOH6tre6HiOOGsAnyW7GHINnP77EP8Sn-MPQ7GU130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP773566.RAcOtFqOH6tre6HiOOGsAnyW7GHINnP77EP8Sn-MPQ7GU130_assertion {
  miriam-gene:8797 a ncit:C16612 .
  
  lld:C0007570 a ncit:C7057 .
  
  dgn-gda:DGN9aedce4eaafb6a1b2720de736d0494c4 sio:SIO_000628 miriam-gene:8797, lld:C0007570;
    a sio:SIO_001121 .
}

dgn-np:NP773566.RAcOtFqOH6tre6HiOOGsAnyW7GHINnP77EP8Sn-MPQ7GU130_provenance {
  dgn-np:NP773566.RAcOtFqOH6tre6HiOOGsAnyW7GHINnP77EP8Sn-MPQ7GU130_assertion dcterms:description
      "[A young woman with the HLA phenotype A1, A2, B5, B8, DR3, DR4 developed RA, idiopathic thrombocytopenic purpura (ITP), pernicious anaemia (PA), Hashimoto's thyroiditis (HT), systemic sclerosis (SS), pancreatic exocrine insufficiency (PEI) and coeliac disease (CD) before dying from vasculitic complications.]. 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:8448621;
    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:NP773566.RAcOtFqOH6tre6HiOOGsAnyW7GHINnP77EP8Sn-MPQ7GU130_publicationInfo {
  this: dcterms:created "2014-10-02T12:39:48+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" .
}