@prefix this: <http://rdf.disgenet.org/resource/nanopub/NP950918.RADc99lYO7wkh08Yv2fdRDiCL8v9koz5TkYp2jKvNkoMs> .
@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:NP950918.RADc99lYO7wkh08Yv2fdRDiCL8v9koz5TkYp2jKvNkoMs130_head {
  this: np:hasAssertion dgn-np:NP950918.RADc99lYO7wkh08Yv2fdRDiCL8v9koz5TkYp2jKvNkoMs130_assertion;
    np:hasProvenance dgn-np:NP950918.RADc99lYO7wkh08Yv2fdRDiCL8v9koz5TkYp2jKvNkoMs130_provenance;
    np:hasPublicationInfo dgn-np:NP950918.RADc99lYO7wkh08Yv2fdRDiCL8v9koz5TkYp2jKvNkoMs130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP950918.RADc99lYO7wkh08Yv2fdRDiCL8v9koz5TkYp2jKvNkoMs130_assertion a np:Assertion .
  
  dgn-np:NP950918.RADc99lYO7wkh08Yv2fdRDiCL8v9koz5TkYp2jKvNkoMs130_provenance a np:Provenance .
  
  dgn-np:NP950918.RADc99lYO7wkh08Yv2fdRDiCL8v9koz5TkYp2jKvNkoMs130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP950918.RADc99lYO7wkh08Yv2fdRDiCL8v9koz5TkYp2jKvNkoMs130_assertion {
  miriam-gene:81494 a ncit:C16612 .
  
  lld:C2931788 a ncit:C7057 .
  
  dgn-gda:DGN6797b14261ae7e88d71276b58cc57657 sio:SIO_000628 miriam-gene:81494, lld:C2931788;
    a sio:SIO_001121 .
}

dgn-np:NP950918.RADc99lYO7wkh08Yv2fdRDiCL8v9koz5TkYp2jKvNkoMs130_provenance {
  dgn-np:NP950918.RADc99lYO7wkh08Yv2fdRDiCL8v9koz5TkYp2jKvNkoMs130_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-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:NP950918.RADc99lYO7wkh08Yv2fdRDiCL8v9koz5TkYp2jKvNkoMs130_publicationInfo {
  this: dcterms:created "2015-08-25T14:47:20+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" .
}