@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP456776.RAr-dv8xXvIu7Lqqa25s0CWludFtJBgIKFg2feHRsuYF8> .
@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:NP456776.RAr-dv8xXvIu7Lqqa25s0CWludFtJBgIKFg2feHRsuYF8130_head {
  this: np:hasAssertion dgn-np:NP456776.RAr-dv8xXvIu7Lqqa25s0CWludFtJBgIKFg2feHRsuYF8130_assertion;
    np:hasProvenance dgn-np:NP456776.RAr-dv8xXvIu7Lqqa25s0CWludFtJBgIKFg2feHRsuYF8130_provenance;
    np:hasPublicationInfo dgn-np:NP456776.RAr-dv8xXvIu7Lqqa25s0CWludFtJBgIKFg2feHRsuYF8130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP456776.RAr-dv8xXvIu7Lqqa25s0CWludFtJBgIKFg2feHRsuYF8130_assertion a np:Assertion .
  
  dgn-np:NP456776.RAr-dv8xXvIu7Lqqa25s0CWludFtJBgIKFg2feHRsuYF8130_provenance a np:Provenance .
  
  dgn-np:NP456776.RAr-dv8xXvIu7Lqqa25s0CWludFtJBgIKFg2feHRsuYF8130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP456776.RAr-dv8xXvIu7Lqqa25s0CWludFtJBgIKFg2feHRsuYF8130_assertion {
  miriam-gene:81494 a ncit:C16612 .
  
  lld:C0268743 a ncit:C7057 .
  
  dgn-gda:DGNd3641740116c3066f7ff84707a33d604 sio:SIO_000628 miriam-gene:81494, lld:C0268743;
    a sio:SIO_001121 .
}

dgn-np:NP456776.RAr-dv8xXvIu7Lqqa25s0CWludFtJBgIKFg2feHRsuYF8130_provenance {
  dgn-np:NP456776.RAr-dv8xXvIu7Lqqa25s0CWludFtJBgIKFg2feHRsuYF8130_assertion dcterms:description
      "[In this review, we discuss how studying CFHR5 nephropathy can contribute to our understanding of the role of complement in kidney diseases such as dense deposit disease, C3 glomerulonephritis and atypical haemolytic uraemic syndrome.]. 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:22065842;
    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:NP456776.RAr-dv8xXvIu7Lqqa25s0CWludFtJBgIKFg2feHRsuYF8130_publicationInfo {
  this: dcterms:created "2014-10-02T12:36:32+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" .
}