@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP649008.RAmcN4NZe0GHz_1cmZz_ovujKyoCd8Bnp5MOETyzO1qMU> .
@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:NP649008.RAmcN4NZe0GHz_1cmZz_ovujKyoCd8Bnp5MOETyzO1qMU130_head {
  this: np:hasAssertion dgn-np:NP649008.RAmcN4NZe0GHz_1cmZz_ovujKyoCd8Bnp5MOETyzO1qMU130_assertion;
    np:hasProvenance dgn-np:NP649008.RAmcN4NZe0GHz_1cmZz_ovujKyoCd8Bnp5MOETyzO1qMU130_provenance;
    np:hasPublicationInfo dgn-np:NP649008.RAmcN4NZe0GHz_1cmZz_ovujKyoCd8Bnp5MOETyzO1qMU130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP649008.RAmcN4NZe0GHz_1cmZz_ovujKyoCd8Bnp5MOETyzO1qMU130_assertion a np:Assertion .
  
  dgn-np:NP649008.RAmcN4NZe0GHz_1cmZz_ovujKyoCd8Bnp5MOETyzO1qMU130_provenance a np:Provenance .
  
  dgn-np:NP649008.RAmcN4NZe0GHz_1cmZz_ovujKyoCd8Bnp5MOETyzO1qMU130_publicationInfo a
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}

dgn-np:NP649008.RAmcN4NZe0GHz_1cmZz_ovujKyoCd8Bnp5MOETyzO1qMU130_assertion {
  miriam-gene:5111 a ncit:C16612 .
  
  lld:C0085413 a ncit:C7057 .
  
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    a sio:SIO_001121 .
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dgn-np:NP649008.RAmcN4NZe0GHz_1cmZz_ovujKyoCd8Bnp5MOETyzO1qMU130_provenance {
  dgn-np:NP649008.RAmcN4NZe0GHz_1cmZz_ovujKyoCd8Bnp5MOETyzO1qMU130_assertion dcterms:description
      "[In this study, which used immunohistochemical methods with an antibody to proliferating cell nuclear antigen (PCNA), the proliferation index (PI) (percentage of PCNA positive cell nuclei among epithelial cells lining the renal cysts) was determined in 10 cases of autosomal dominant polycystic kidney disease (ADPKD), 8 cases of autosomal recessive polycystic kidney disease (ARPKD), and 8 cases of acquired cystic kidney disease (ACKD).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine."@en;
    wi:evidence dgn-void:source_evidence_literature;
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    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:NP649008.RAmcN4NZe0GHz_1cmZz_ovujKyoCd8Bnp5MOETyzO1qMU130_publicationInfo {
  this: dcterms:created "2014-10-02T12:38:31+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;
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    pav:version "v2.1.0.0" .
  
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