@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 rdfs: <http://www.w3.org/2000/01/rdf-schema#> .
@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#> .

nalt:7778_def
  rdf:value "Una mutación en la cual un codón muta de forma que dirige la incorporación de un aminoácido diferente. Esta sustitución puede conducir a un producto inestable o inactivo."@es, "A mutation in which a codon is mutated to one directing the incorporation of a different amino acid. This substitution may result in an inactive or unstable product."@en ;
  dc:source "Medical Subject Headings" ;
  a <https://lod.nal.usda.gov/naltv#Definition> .

nalt:7777
  skos:prefLabel "mutación"@es, "mutation"@en ;
  a <https://lod.nal.usda.gov/naltv#Topic>, skos:Concept ;
  skos:narrower nalt:7778 .

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

nalt:7778
  skos:inScheme <https://lod.nal.usda.gov/nalt> ;
  a <https://lod.nal.usda.gov/naltv#Topic>, skos:Concept ;
  skos:related nalt:53145, nalt:7776 ;
  skos:broader nalt:7777 ;
  skos:hiddenLabel "missense mutations"@en, "missense-mutation"@en ;
  dc:modified "2013-01-14"^^xsd:date ;
  dc:created "2006-01-19"^^xsd:date ;
  ns0:marc001 "23789" ;
  skos:prefLabel "mutación missense"@es, "missense mutation"@en ;
  skos:definition nalt:7778_def .

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

nalt:53145
  skos:prefLabel "mutación puntual"@es, "point mutation"@en ;
  a ns0:Topic, skos:Concept ;
  skos:related nalt:7778 .

nalt:7776
  skos:prefLabel "sustitución de aminoácidos"@es, "amino acid substitution"@en ;
  a ns0:Topic, skos:Concept ;
  skos:related nalt:7778 .