Galnet - Galician WordNet 3.0

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ili-30-05437600-n CILI: i65520
WordNet Domains: biology
SUMO Ontology: Molecule+
Top Ontology: Substance+
Basic Level Concept: 05436752-n cistron
Epinonyms: [2] genetics
[2] genetics |0.98|
[1] ili-30-05436752-n (category) |0.95|
[0] ili-30-05437600-n (has_hyperonym) |1|
Polarity:
  positive negative
SentiWordNet: 0 0
ML-SentiCon: 0 0
Time:
  past present future atemporal
TempoWordNet: 0 0 0 1

Explore the terminological domain with [Termonet]
GL Variants
- xene_dominante · [RILG] [DRAG]
o xene dominante para os ollos castaños
Gloss
xene que produce o mesmo fenotipo do organismo sexa ou non idéntico ao alelo.
ES Variants
- gen_dominante
EN Variants
- dominant_gene
the dominant gene for brown eyes
Gloss
gene that produces the same phenotype in the organism whether or not its allele identical
Lexical relations in WordNet via ILI (9) - Show / Hide graph:
Hyperonyms
(has_hyperonym)
05436752-n: (genetics) a segment of DNA that is involved in producing a polypeptide chain; it can include regions preceding and following the coding DNA as well as introns between the exons; it is considered a unit of heredity
Glosses
(gloss)
00004475-n: a living thing that has (or can develop) the ability to act or function independently
Glosses
(gloss)
00024073-r: negation of a word or group of words
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)
05436752-n: (genetics) a segment of DNA that is involved in producing a polypeptide chain; it can include regions preceding and following the coding DNA as well as introns between the exons; it is considered a unit of heredity
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)
04923299-n: hereditary pattern in which a dominant gene on the X chromosome causes a characteristic to be manifested in the offspring