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

nalt:261891
  skos:prefLabel "supresión genética"@es, "genetic suppression"@en ;
  a <https://lod.nal.usda.gov/naltv#Topic>, skos:Concept ;
  skos:related nalt:53832 .

nalt:53832
  skos:related nalt:42606, nalt:261891, nalt:27635 ;
  skos:hiddenLabel "nonsense mutations"@en, "opal-mutations"@en, "amber nonsense codon"@en, "nonsense amber mutation"@en, "ochre nonsense codon"@en, "amber mutations"@en, "opal-mutation"@en, "opal mutations"@en, "nonsense-mutation"@en, "amber nonsense codons"@en ;
  a skos:Concept, <https://lod.nal.usda.gov/naltv#Topic> ;
  ns0:marc001 "40897" ;
  skos:exactMatch <http://id.loc.gov/authorities/subjects/sh85092358> ;
  dc:created "2006-01-19"^^xsd:date ;
  skos:prefLabel "mutación sin sentido"@es, "nonsense mutation"@en ;
  skos:broader nalt:7777 ;
  skos:altLabel "amber mutation"@en, "opal mutation"@en, "amber nonsense mutation"@en, "opal nonsense mutation"@en, "ochre nonsense mutation"@en ;
  skos:definition nalt:53832_def ;
  skos:inScheme <https://lod.nal.usda.gov/nalt> ;
  dc:modified "2016-03-01"^^xsd:date .

nalt:42606
  skos:prefLabel "genes supresores"@es, "suppressor genes"@en ;
  a ns0:Topic, skos:Concept ;
  skos:related nalt:53832 .

nalt:7777
  skos:prefLabel "mutación"@es, "mutation"@en ;
  a ns0:Topic, skos:Concept ;
  skos:narrower nalt:53832 .

ns0:Topic
  rdfs:label "Topic"@en ;
  a owl:Class .

nalt:27635
  skos:prefLabel "codón de detención"@es, "stop codon"@en ;
  a ns0:Topic, skos:Concept ;
  skos:related nalt:53832 .

nalt:53832_def
  rdf:value "Mutación en la que el sentido del codón (que codifica un aminoácido) se transforma en la misma secuencia de un codón de detención. Esto causa la terminación prematura de la traducción de la proteína, lo que resulta en la producción de proteínas truncadas que pueden ser no funcionales."@es, "A mutation in which a sense codon (which codes for an amino acid) is converted to the same sequence as a stop codon. This abnormal occurrence causes premature termination of protein translation resulting in the production of truncated proteins which may be non-functional."@en ;
  dc:source "NAL Thesaurus Staff" ;
  a ns0:Definition .

<https://lod.nal.usda.gov/nalt>
  rdfs:label "NALT Full"@en ;
  a skos:ConceptScheme .