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

nalt:31335
  skos:prefLabel "enfermedades pancreáticas"@es, "pancreatic diseases"@en ;
  a <https://lod.nal.usda.gov/naltv#Topic>, skos:Concept ;
  skos:narrower nalt:31334 .

nalt:746
  skos:prefLabel "fibrosis"@es, "fibrosis"@en ;
  a <https://lod.nal.usda.gov/naltv#Topic>, skos:Concept ;
  skos:related nalt:31334 .

nalt:347
  skos:prefLabel "enfermedades respiratorias"@es, "respiratory tract diseases"@en ;
  a <https://lod.nal.usda.gov/naltv#Topic>, skos:Concept ;
  skos:narrower nalt:31334 .

<https://lod.nal.usda.gov/nalt-core>
  rdfs:label "NALT Core"@es, "NALT Core"@en ;
  a skos:ConceptScheme .

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

nalt:18968
  skos:prefLabel "trastornos genéticos"@es, "genetic disorders"@en ;
  a <https://lod.nal.usda.gov/naltv#Topic>, skos:Concept ;
  skos:narrower nalt:31334 .

nalt:31334
  skos:broader nalt:347, nalt:31335, nalt:18968 ;
  skos:exactMatch <http://id.loc.gov/authorities/subjects/sh85035204>, <http://id.cabi.org/cabt/35959>, <http://id.agrisemantics.org/gacs/C16511> ;
  skos:prefLabel "cystic fibrosis"@en, "fibrosis quística"@es ;
  skos:definition nalt:31334_def ;
  a <https://lod.nal.usda.gov/naltv#Topic>, skos:Concept ;
  skos:inScheme <https://lod.nal.usda.gov/nalt-core>, <https://lod.nal.usda.gov/nalt> ;
  ns0:marc001 "10886" ;
  dc:created "2006-01-19"^^xsd:date ;
  skos:hiddenLabel "cystic-fibrosis"@en ;
  dc:modified "2018-05-15"^^xsd:date ;
  skos:related nalt:746 .

nalt:31334_def
  rdf:value "Enfermedad hereditaria de las glándulas exocrinas que con mayor frecuencia afecta el páncreas, el sistema respiratorio y las glándulas sudoríparas; comienza generalmente en la infancia y se caracteriza por infecciones respiratorias crónicas, insuficiencia pancreática, y susceptibilidad al agotamiento por calor. La cirrosis hepática es común en la niñez y puede producir hipertensión portal, esplenomegalia e hiperesplenismo."@es, "An autosomal recessive genetic disease of the exocrine glands. It is caused by mutations in the gene encoding the cystic fibrosis transmembrane conductance regulator expressed in several organs including the lung, the pancreas, the biliary system, and the sweat glands."@en ;
  dc:source "Medical Subject Headings" ;
  a ns0:Definition .