@prefix dct: <http://purl.org/dc/terms/> .
@prefix orcid: <http://orcid.org/> .
@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP44102.RAtSlvGTKcMpTrKYfMccc9eMX7sn-BHLQbeiRelvjdw7o> .
@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 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:NP44102.RAtSlvGTKcMpTrKYfMccc9eMX7sn-BHLQbeiRelvjdw7o130_head {
  this: np:hasAssertion dgn-np:NP44102.RAtSlvGTKcMpTrKYfMccc9eMX7sn-BHLQbeiRelvjdw7o130_assertion;
    np:hasProvenance dgn-np:NP44102.RAtSlvGTKcMpTrKYfMccc9eMX7sn-BHLQbeiRelvjdw7o130_provenance;
    np:hasPublicationInfo dgn-np:NP44102.RAtSlvGTKcMpTrKYfMccc9eMX7sn-BHLQbeiRelvjdw7o130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP44102.RAtSlvGTKcMpTrKYfMccc9eMX7sn-BHLQbeiRelvjdw7o130_assertion a np:Assertion .
  
  dgn-np:NP44102.RAtSlvGTKcMpTrKYfMccc9eMX7sn-BHLQbeiRelvjdw7o130_provenance a np:Provenance .
  
  dgn-np:NP44102.RAtSlvGTKcMpTrKYfMccc9eMX7sn-BHLQbeiRelvjdw7o130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP44102.RAtSlvGTKcMpTrKYfMccc9eMX7sn-BHLQbeiRelvjdw7o130_assertion {
  miriam-gene:2212 a ncit:C16612 .
  
  lld:C0024141 a ncit:C7057 .
  
  dgn-gda:DGN77a201706c6ce374b4411fb71caad8e3 sio:SIO_000628 miriam-gene:2212, lld:C0024141;
    a sio:SIO_001122 .
}

dgn-np:NP44102.RAtSlvGTKcMpTrKYfMccc9eMX7sn-BHLQbeiRelvjdw7o130_provenance {
  dgn-np:NP44102.RAtSlvGTKcMpTrKYfMccc9eMX7sn-BHLQbeiRelvjdw7o130_assertion dct:description
      "[ The results of this explorative study support the view that the FcgammaRIIa/IIIa and IIIb polymorphisms constitute factors influencing clinical manifestations and the disease course of SLE but do not represent genetic risk factors for the occurrence of SLE. Higher frequencies of clinical symptoms, haematological and immunological abnormalities as well as an earlier onset of clinical symptoms, haematological and immunological markers of active disease were found in patients with the IIA-R/R131 genotype and the double negative and triple negative genotypes.]. 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:12176802;
    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:NP44102.RAtSlvGTKcMpTrKYfMccc9eMX7sn-BHLQbeiRelvjdw7o130_publicationInfo {
  this: dct:created "2014-10-02T12:32:20+02:00"^^xsd:dateTime;
    dct:rights <http://opendatacommons.org/licenses/odbl/1.0/>;
    dct:rightsHolder dgn-void:IBIGroup;
    dct:subject sio:SIO_000983;
    prv:usedData dgn-void:disgenetrdf;
    pav:authoredBy orcid:0000-0001-5999-6269, orcid:0000-0002-7534-7661, orcid:0000-0002-9383-528X,
      orcid:0000-0003-0169-8159, orcid:0000-0003-1244-7654;
    pav:createdBy orcid:0000-0003-0169-8159;
    pav:version "v2.1.0.0" .
  
  dgn-void:disgenetrdf pav:version "v2.1.0" .
}