Galnet - WordNet 3.0 do Galego

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Pescudas no Galnet

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ili-30-05438315-n CILI: i65523
WordNet Domains: biology
SUMO Ontology: Molecule+
Top Ontology: Substance+
Basic Level Concept: 05436752-n cistron
Epinonyms: [2] genetics
[2] genetics |0,98|
[1] ili-30-05437785-n (category) |0,95|
[0] ili-30-05438315-n (has_hyperonym) |1|
Polaridade:
  positivo negativo
SentiWordNet: 0 0
ML-SentiCon: 0.125 0
Tempo:
  pasado presente futuro atemporal
TempoWordNet: 0 0 0 1

Explorar o ámbito terminolóxico en [Termonet]
GL Variantes
- alelo_recesivo · [RILG] [DRAG]
- recesivo [reθeˈsiβo̝] [reθɛˈsiβo̝] · [RILG] [DRAG]
Glosa
alelo que produce o seu fenotipo característico só cando o seu alelo par é idéntico
ES Variantes
- alelo_recesivo
- recesivo
EN Variantes
- recessive [rə'sɛsɪv]
- recessive_allele
Glosa
an allele that produces its characteristic phenotype only when its paired allele is identical
Relacións léxico-semánticas no WordNet vía ILI (8) - Amosar / Agochar gráfico:
Hyperonyms
(has_hyperonym)
05437785-n: (genetics) either of a pair (or series) of alternative forms of a gene that can occupy the same locus on a particular chromosome and that control the same character
Glosses
(gloss)
00356926-a: typical or distinctive
Glosses
(gloss)
01752884-v: cause to happen, occur or exist
Glosses
(gloss)
02064127-a: exactly alike; incapable of being perceived as different
Glosses
(gloss)
04933852-n: what an organism looks like as a consequence of the interaction of its genotype and the environment
Glosses
(gloss)
05437785-n: (genetics) either of a pair (or series) of alternative forms of a gene that can occupy the same locus on a particular chromosome and that control the same character
Glosses
(rgloss)
00851316-n: a cross between an organism whose genotype for a certain trait is unknown and an organism that is homozygous recessive for that trait so the unknown genotype can be determined from that of the offspring
Glosses
(rgloss)
14157163-n: hereditary disease (autosomal recessive) consisting of an error is mucopolysaccharide metabolism; characterized by severe abnormalities in development of skeletal cartilage and bone and mental retardation