@prefix this: <http://rdf.disgenet.org/resource/nanopub/NP454973.RAjaW05iPLdMxYfYZncwKIPkeHpIzNeA6nBkOUFHbwXH0> .
@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/v3.0.0/void/> .

dgn-np:NP454973.RAjaW05iPLdMxYfYZncwKIPkeHpIzNeA6nBkOUFHbwXH0130_head {
  this: np:hasAssertion dgn-np:NP454973.RAjaW05iPLdMxYfYZncwKIPkeHpIzNeA6nBkOUFHbwXH0130_assertion;
    np:hasProvenance dgn-np:NP454973.RAjaW05iPLdMxYfYZncwKIPkeHpIzNeA6nBkOUFHbwXH0130_provenance;
    np:hasPublicationInfo dgn-np:NP454973.RAjaW05iPLdMxYfYZncwKIPkeHpIzNeA6nBkOUFHbwXH0130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP454973.RAjaW05iPLdMxYfYZncwKIPkeHpIzNeA6nBkOUFHbwXH0130_assertion a np:Assertion .
  
  dgn-np:NP454973.RAjaW05iPLdMxYfYZncwKIPkeHpIzNeA6nBkOUFHbwXH0130_provenance a np:Provenance .
  
  dgn-np:NP454973.RAjaW05iPLdMxYfYZncwKIPkeHpIzNeA6nBkOUFHbwXH0130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP454973.RAjaW05iPLdMxYfYZncwKIPkeHpIzNeA6nBkOUFHbwXH0130_assertion {
  miriam-gene:3123 a ncit:C16612 .
  
  lld:C0022408 a ncit:C7057 .
  
  dgn-gda:DGNc63af906f6cf81dc7c380d3a2ae60a01 sio:SIO_000628 miriam-gene:3123, lld:C0022408;
    a sio:SIO_001121 .
}

dgn-np:NP454973.RAjaW05iPLdMxYfYZncwKIPkeHpIzNeA6nBkOUFHbwXH0130_provenance {
  dgn-np:NP454973.RAjaW05iPLdMxYfYZncwKIPkeHpIzNeA6nBkOUFHbwXH0130_assertion dcterms:description
      "[In the light of associations previously described between DR4, DQw7, the C4B null allele and Felty's syndrome, and between Dw14, the C4A null allele and rheumatoid vasculitis, we have looked for associations between these and other DRB1, DQB, DQA and C4 encoded variants, and articular disease severity assessed radiologically in 119 subjects with RA but without major extra-articular features.]. 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:8401999;
    prov:wasDerivedFrom dgn-void:befree-20150227;
    prov:wasGeneratedBy eco:ECO_0000203 .
  
  dgn-void:befree-20150227 pav:importedOn "2015-02-27"^^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:NP454973.RAjaW05iPLdMxYfYZncwKIPkeHpIzNeA6nBkOUFHbwXH0130_publicationInfo {
  this: dcterms:created "2015-08-25T14:42:06+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 "v3.0.0.0" .
  
  dgn-void:disgenetv3.0rdf pav:version "v3.0.0" .
}