@prefix this: <http://rdf.disgenet.org/resource/nanopub/NP1305214.RAtCHKKW5TTa3hrILaNj0i6i2aSlDYLHx4LsMWec2k7jA> .
@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/v4.0.0/void/> .

dgn-np:NP1305214.RAtCHKKW5TTa3hrILaNj0i6i2aSlDYLHx4LsMWec2k7jA130_head {
  this: np:hasAssertion dgn-np:NP1305214.RAtCHKKW5TTa3hrILaNj0i6i2aSlDYLHx4LsMWec2k7jA130_assertion;
    np:hasProvenance dgn-np:NP1305214.RAtCHKKW5TTa3hrILaNj0i6i2aSlDYLHx4LsMWec2k7jA130_provenance;
    np:hasPublicationInfo dgn-np:NP1305214.RAtCHKKW5TTa3hrILaNj0i6i2aSlDYLHx4LsMWec2k7jA130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP1305214.RAtCHKKW5TTa3hrILaNj0i6i2aSlDYLHx4LsMWec2k7jA130_assertion a np:Assertion .
  
  dgn-np:NP1305214.RAtCHKKW5TTa3hrILaNj0i6i2aSlDYLHx4LsMWec2k7jA130_provenance a np:Provenance .
  
  dgn-np:NP1305214.RAtCHKKW5TTa3hrILaNj0i6i2aSlDYLHx4LsMWec2k7jA130_publicationInfo
    a np:PublicationInfo .
}

dgn-np:NP1305214.RAtCHKKW5TTa3hrILaNj0i6i2aSlDYLHx4LsMWec2k7jA130_assertion {
  miriam-gene:718 a ncit:C16612 .
  
  lld:C0024141 a ncit:C7057 .
  
  dgn-gda:DGN6c813d0ef2a7c77feff3b2bc3545f4db sio:SIO_000628 miriam-gene:718, lld:C0024141;
    a sio:SIO_001121 .
}

dgn-np:NP1305214.RAtCHKKW5TTa3hrILaNj0i6i2aSlDYLHx4LsMWec2k7jA130_provenance {
  dgn-np:NP1305214.RAtCHKKW5TTa3hrILaNj0i6i2aSlDYLHx4LsMWec2k7jA130_assertion dcterms:description
      "[The inherited partial deficiency of erythrocyte C3b receptors in patients with SLE, and the absence of glomerular C3b receptors in these patients with proliferative glomerulonephritis may contribute to systemic and organ-specific abnormalities in the clearance of immune complexes that contribute to the pathogenesis of this disease.]. 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:6227098;
    prov:wasDerivedFrom dgn-void:befree-2016;
    prov:wasGeneratedBy eco:ECO_0000203 .
  
  dgn-void:befree-2016 pav:importedOn "2016-02-19"^^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:NP1305214.RAtCHKKW5TTa3hrILaNj0i6i2aSlDYLHx4LsMWec2k7jA130_publicationInfo {
  this: dcterms:created "2016-05-13T12:51:37+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 "v4.0.0.0" .
  
  dgn-void:disgenetv3.0rdf pav:version "v4.0.0" .
}