@prefix rdfs: <http://www.w3.org/2000/01/rdf-schema#> .
@prefix nalt: <https://lod.nal.usda.gov/nalt/> .
@prefix rdf: <http://www.w3.org/1999/02/22-rdf-syntax-ns#> .
@prefix dc: <http://purl.org/dc/terms/> .
@prefix skos: <http://www.w3.org/2004/02/skos/core#> .
@prefix owl: <http://www.w3.org/2002/07/owl#> .
@prefix xsd: <http://www.w3.org/2001/XMLSchema#> .
@prefix ns0: <https://lod.nal.usda.gov/naltv#> .

<https://lod.nal.usda.gov/naltv#marc001> rdfs:label "Field 001 in MARC Authority Format"@en .
nalt:219148_def
  a <https://lod.nal.usda.gov/naltv#Definition> ;
  rdf:value "Trastorno genético con herencia autosómica recesiva caracterizado por el desarrollo de múltiples quistes en ambos riñones y de lesiones hepáticas asociadas. Suelen presentarse manifestaciones graves al nacer, con un alto grado de mortalidad perinatal."@es, "A genetic disorder with autosomal recessive inheritance, characterized by multiple cysts in both kidneys and associated liver lesions. Serious manifestations are usually present at birth with high perinatal mortality."@en ;
  dc:source "Medical Subject Headings 2014" .

<https://lod.nal.usda.gov/nalt>
  a skos:ConceptScheme ;
  rdfs:label "NALT Full"@en .

<https://lod.nal.usda.gov/naltv#Topic>
  a owl:Class ;
  rdfs:label "Topic"@en .

nalt:219148
  a <https://lod.nal.usda.gov/naltv#Topic>, skos:Concept ;
  dc:created "2014-06-19"^^xsd:date ;
  dc:modified "2017-11-17"^^xsd:date ;
  skos:altLabel "infantile polycystic kidney disease type I"@en ;
  skos:broader nalt:219143 ;
  skos:definition nalt:219148_def ;
  skos:inScheme <https://lod.nal.usda.gov/nalt> ;
  skos:prefLabel "enfermedad renal poliquística autosómica recesiva"@es, "autosomal recessive polycystic kidney disease"@en ;
  ns0:marc001 "63642" .

nalt:219143
  a ns0:Topic, skos:Concept ;
  skos:narrower nalt:219148 ;
  skos:prefLabel "enfermedades renales poliquísticas"@es, "polycystic kidney diseases"@en .