@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:309787_def
  a <https://lod.nal.usda.gov/naltv#Definition> ;
  rdf:value "Variación en el número de copias de un gen particular que tiene lugar de un individuo a otro."@es, "A copy number variation (CNV) is when the number of copies of a particular gene varies from one individual to the next."@en ;
  dc:source "Talking Glossary of Genetic Terms, NIH" .

<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:309787
  a <https://lod.nal.usda.gov/naltv#Topic>, skos:Concept ;
  dc:created "2017-10-12"^^xsd:date ;
  dc:modified "2018-09-18"^^xsd:date ;
  skos:altLabel "gene copy number variation"@en ;
  skos:broader nalt:10351 ;
  skos:definition nalt:309787_def ;
  skos:inScheme <https://lod.nal.usda.gov/nalt> ;
  skos:prefLabel "copy number variation"@en, "variación en el número de copias"@es ;
  skos:related nalt:324466, nalt:6539 ;
  ns0:marc001 "80824" .

nalt:324466
  a ns0:Topic, skos:Concept ;
  skos:prefLabel "haploinsuficiencia"@es, "haploinsufficiency"@en ;
  skos:related nalt:309787 .

nalt:6539
  a ns0:Topic, skos:Concept ;
  skos:prefLabel "genes"@es, "genes"@en ;
  skos:related nalt:309787 .

nalt:10351
  a ns0:Topic, skos:Concept ;
  skos:narrower nalt:309787 ;
  skos:prefLabel "variación genética"@es, "genetic variation"@en .