@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP426489.RAEEVKroSXJfLhHw-CDXdQsiUfO9oAxtOYL0urxGG_83I> .
@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:NP426489.RAEEVKroSXJfLhHw-CDXdQsiUfO9oAxtOYL0urxGG_83I130_head {
  this: np:hasAssertion dgn-np:NP426489.RAEEVKroSXJfLhHw-CDXdQsiUfO9oAxtOYL0urxGG_83I130_assertion;
    np:hasProvenance dgn-np:NP426489.RAEEVKroSXJfLhHw-CDXdQsiUfO9oAxtOYL0urxGG_83I130_provenance;
    np:hasPublicationInfo dgn-np:NP426489.RAEEVKroSXJfLhHw-CDXdQsiUfO9oAxtOYL0urxGG_83I130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP426489.RAEEVKroSXJfLhHw-CDXdQsiUfO9oAxtOYL0urxGG_83I130_assertion a np:Assertion .
  
  dgn-np:NP426489.RAEEVKroSXJfLhHw-CDXdQsiUfO9oAxtOYL0urxGG_83I130_provenance a np:Provenance .
  
  dgn-np:NP426489.RAEEVKroSXJfLhHw-CDXdQsiUfO9oAxtOYL0urxGG_83I130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP426489.RAEEVKroSXJfLhHw-CDXdQsiUfO9oAxtOYL0urxGG_83I130_assertion {
  miriam-gene:60498 a ncit:C16612 .
  
  lld:C0017658 a ncit:C7057 .
  
  dgn-gda:DGNe319ada55ed96af35c4c90ce090b7aa6 sio:SIO_000628 miriam-gene:60498, lld:C0017658;
    a sio:SIO_001121 .
}

dgn-np:NP426489.RAEEVKroSXJfLhHw-CDXdQsiUfO9oAxtOYL0urxGG_83I130_provenance {
  dgn-np:NP426489.RAEEVKroSXJfLhHw-CDXdQsiUfO9oAxtOYL0urxGG_83I130_assertion dcterms:description
      "[Mutations, genetic deletions, duplications or rearrangements in the individual CFHR genes are associated with a number of diseases including atypical hemolytic uremic syndrome (aHUS), C3 glomerulopathies (C3 glomerulonephritis (C3GN), dense deposit disease (DDD) and CFHR5 nephropathy), IgA nephropathy, age related macular degeneration (AMD) and systemic lupus erythematosus (SLE).]. 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:23830046;
    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:NP426489.RAEEVKroSXJfLhHw-CDXdQsiUfO9oAxtOYL0urxGG_83I130_publicationInfo {
  this: dcterms:created "2014-10-02T12:36:13+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" .
}