@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP862702.RADkF_UYApMg5KY3KCFd9KHhBh7ZOcAY2iY83h49zXsm0> .
@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:NP862702.RADkF_UYApMg5KY3KCFd9KHhBh7ZOcAY2iY83h49zXsm0130_head {
  this: np:hasAssertion dgn-np:NP862702.RADkF_UYApMg5KY3KCFd9KHhBh7ZOcAY2iY83h49zXsm0130_assertion;
    np:hasProvenance dgn-np:NP862702.RADkF_UYApMg5KY3KCFd9KHhBh7ZOcAY2iY83h49zXsm0130_provenance;
    np:hasPublicationInfo dgn-np:NP862702.RADkF_UYApMg5KY3KCFd9KHhBh7ZOcAY2iY83h49zXsm0130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP862702.RADkF_UYApMg5KY3KCFd9KHhBh7ZOcAY2iY83h49zXsm0130_assertion a np:Assertion .
  
  dgn-np:NP862702.RADkF_UYApMg5KY3KCFd9KHhBh7ZOcAY2iY83h49zXsm0130_provenance a np:Provenance .
  
  dgn-np:NP862702.RADkF_UYApMg5KY3KCFd9KHhBh7ZOcAY2iY83h49zXsm0130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP862702.RADkF_UYApMg5KY3KCFd9KHhBh7ZOcAY2iY83h49zXsm0130_assertion {
  miriam-gene:140805 a ncit:C16612 .
  
  lld:C0027697 a ncit:C7057 .
  
  dgn-gda:DGNc52baaa7de4cdd2be58270462de24cd4 sio:SIO_000628 miriam-gene:140805, lld:C0027697;
    a sio:SIO_001121 .
}

dgn-np:NP862702.RADkF_UYApMg5KY3KCFd9KHhBh7ZOcAY2iY83h49zXsm0130_provenance {
  dgn-np:NP862702.RADkF_UYApMg5KY3KCFd9KHhBh7ZOcAY2iY83h49zXsm0130_assertion dcterms:description
      "[GM and KM immunoglobulin (Ig) allotypes and their interactions with HLA antigens have been analyzed in various autoimmune diseases: multiple sclerosis, rheumatoid arthritis, insulin-dependent diabetes mellitus (IDDM), systemic lupus erythematosus, coeliac disease, Crohn's 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:8781716;
    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:NP862702.RADkF_UYApMg5KY3KCFd9KHhBh7ZOcAY2iY83h49zXsm0130_publicationInfo {
  this: dcterms:created "2014-10-02T12:40:47+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" .
}