@prefix owl: <http://www.w3.org/2002/07/owl#> .
@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#> .

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

nalt:324466_def
  a <https://lod.nal.usda.gov/naltv#Definition> ;
  rdf:value "A copy number variation that results in reduced gene dosage due to any loss-of-function mutation. The loss of heterozygosity is associated with abnormal phenotypes or diseased states because the remaining gene is insufficient."@en, "Variación en el número de copias que da lugar a una dosis génica reducida como resultado de una mutación de pérdida funcional. La pérdida de heterocigosidad se asocia a fenotipos anormales o enfermedades, dado que el gen restante resulta insuficiente."@es ;
  dc:source "Medical Subject Headings" .

nalt:324466 skos:definition nalt:324466_def .