@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:324472_def
  a <https://lod.nal.usda.gov/naltv#Definition> ;
  rdf:value "The loss of one allele at a specific locus, caused by a deletion mutation; or loss of a chromosome from a chromosome pair, resulting in abnormal hemizygosity. It is detected when heterozygous markers for a locus appear monomorphic because one of the alleles was deleted."@en, "Pérdida de un alelo en un locus específico, causada por una mutación de deleción, o pérdida de uno de los cromosomas de un par, que produce una heterocigosidad anormal. Se detecta cuando los marcadores heterocigotas de un locus se presentan monomórficos debido a la eliminación de uno de los alelos."@es ;
  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:324472
  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 "allelic loss"@en ;
  skos:broader nalt:324468 ;
  skos:definition nalt:324472_def ;
  skos:inScheme <https://lod.nal.usda.gov/nalt> ;
  skos:narrower nalt:324466 ;
  skos:prefLabel "pérdida de heterocigosidad"@es, "loss of heterozygosity"@en ;
  skos:related nalt:25836, nalt:42713 ;
  ns0:marc001 "88468" .

nalt:25836
  a ns0:Topic, skos:Concept ;
  skos:prefLabel "chromosome elimination"@en, "eliminación cromosómica"@es ;
  skos:related nalt:324472 .

nalt:324466
  a ns0:Topic, skos:Concept ;
  skos:broader nalt:324472 ;
  skos:prefLabel "haploinsuficiencia"@es, "haploinsufficiency"@en .

nalt:324468
  a ns0:Topic, skos:Concept ;
  skos:narrower nalt:324472 ;
  skos:prefLabel "allelic imbalance"@en, "desequilibrio alélico"@es .

nalt:42713
  a ns0:Topic, skos:Concept ;
  skos:prefLabel "heterozygosity"@en, "heterocigosidad"@es ;
  skos:related nalt:324472 .