@prefix this: <http://rdf.disgenet.org/resource/nanopub/NP616128.RAHMrQCQZ8FunlqSJWcxYNl6f5tRjot8Z0VZozafR28lk> .
@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:NP616128.RAHMrQCQZ8FunlqSJWcxYNl6f5tRjot8Z0VZozafR28lk130_head {
  this: np:hasAssertion dgn-np:NP616128.RAHMrQCQZ8FunlqSJWcxYNl6f5tRjot8Z0VZozafR28lk130_assertion;
    np:hasProvenance dgn-np:NP616128.RAHMrQCQZ8FunlqSJWcxYNl6f5tRjot8Z0VZozafR28lk130_provenance;
    np:hasPublicationInfo dgn-np:NP616128.RAHMrQCQZ8FunlqSJWcxYNl6f5tRjot8Z0VZozafR28lk130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP616128.RAHMrQCQZ8FunlqSJWcxYNl6f5tRjot8Z0VZozafR28lk130_assertion a np:Assertion .
  
  dgn-np:NP616128.RAHMrQCQZ8FunlqSJWcxYNl6f5tRjot8Z0VZozafR28lk130_provenance a np:Provenance .
  
  dgn-np:NP616128.RAHMrQCQZ8FunlqSJWcxYNl6f5tRjot8Z0VZozafR28lk130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP616128.RAHMrQCQZ8FunlqSJWcxYNl6f5tRjot8Z0VZozafR28lk130_assertion {
  miriam-gene:5187 a ncit:C16612 .
  
  lld:C0022658 a ncit:C7057 .
  
  dgn-gda:DGN340bfdf9abb7e5220059fc852a746edb sio:SIO_000628 miriam-gene:5187, lld:C0022658;
    a sio:SIO_001121 .
}

dgn-np:NP616128.RAHMrQCQZ8FunlqSJWcxYNl6f5tRjot8Z0VZozafR28lk130_provenance {
  dgn-np:NP616128.RAHMrQCQZ8FunlqSJWcxYNl6f5tRjot8Z0VZozafR28lk130_assertion dcterms:description
      "[Adjusting for family age at nephropathy, gender, and ancestry, presence of JCV genomic DNA in urine and APOL1 risk alleles were significantly negatively associated with elevated serum cystatin C, albuminuria (albumin-to-creatinine ratio over 30 mg/g), and kidney disease defined as an eGFR under 60 ml/min per 1.73 m(2) and/or albuminuria in an additive (APOL1 plus JCV) model.]. 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:23677244;
    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:NP616128.RAHMrQCQZ8FunlqSJWcxYNl6f5tRjot8Z0VZozafR28lk130_publicationInfo {
  this: dcterms:created "2015-08-25T14:43:48+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" .
}