@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:324464_def
  a <https://lod.nal.usda.gov/naltv#Definition> ;
  rdf:value "Individuo que tiene solo un alelo en un lugar determinado debido a la pérdida del otro alelo por una mutación (por ejemplo, una deleción cromosómica)."@es, "An individual having only one allele at a given locus because of the loss of the other allele through a mutation (e.g., chromosome deletion)."@en ;
  dc:source "Medical Subject Headings" .

<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:324464
  a <https://lod.nal.usda.gov/naltv#Topic>, skos:Concept ;
  dc:created "2018-09-18"^^xsd:date ;
  dc:modified "2018-11-14"^^xsd:date ;
  skos:altLabel "hemizygosity"@en ;
  skos:broader nalt:17553 ;
  skos:definition nalt:324464_def ;
  skos:inScheme <https://lod.nal.usda.gov/nalt> ;
  skos:prefLabel "hemicigoto"@es, "hemizygote"@en ;
  skos:related nalt:25836, nalt:6537 ;
  ns0:marc001 "87735" .

nalt:25836
  a ns0:Topic, skos:Concept ;
  skos:prefLabel "chromosome elimination"@en, "eliminación cromosómica"@es ;
  skos:related nalt:324464 .

nalt:6537
  a ns0:Topic, skos:Concept ;
  skos:prefLabel "alelos"@es, "alleles"@en ;
  skos:related nalt:324464 .

nalt:17553
  a ns0:Topic, skos:Concept ;
  skos:narrower nalt:324464 ;
  skos:prefLabel "genotipo"@es, "genotype"@en .