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"synonym": [- "secondary alpha-hydroxy ketones",
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],-
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"synonym": [- "Knop ME (related)",
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"synonym": [- "abnormal stratification treatment (narrow)"
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"synonym": [- "Aminosugars",
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"synonym": [],-
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"synonym": [],-
"definition": [- "The radioactive isotope of hydrogen with relative atomic mass 3.016049 and half-life of 12.33 years (from Greek taurhoiotatauomicronsigma, third)."
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"synonym": [],-
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"synonym": [- "cholinergic drugs",
- "cholinomimetic",
- "cholinergic agent"
],-
"definition": [- "Any drug used for its actions on cholinergic systems. Included here are agonists and antagonists, drugs that affect the life cycle of acetylcholine, and drugs that affect the survival of cholinergic neurons."
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{- "prefLabel": "salicylic acid exposure",
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"synonym": [- "salicylic acid treatment (narrow)"
],-
"definition": [- "An organic chemical exposure (PECO:0001003) involving the application of salicylic acid (CHEBI:16914)."
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{- "prefLabel": "calcium nutrient exposure",
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"synonym": [- "calcium nutrient treatment (narrow)"
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"definition": [- "The treatment involving exposure of plant to macronutrient calcium as supplement to study various types of responses."
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{- "prefLabel": "phosphate(3-)",
-
"synonym": [- "tetraoxophosphate(V)",
- "tetraoxophosphate(3-)",
- "phosphate",
- "tetraoxidophosphate(3-)"
],-
"definition": [- "A phosphate ion that is the conjugate base of hydrogenphosphate."
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"@context": {- "self": "http://www.w3.org/2002/07/owl#Class",
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{- "prefLabel": "terpene ketone",
-
"definition": [- "Any terpenoid which contains a keto group."
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"links": {- "self": "https://data.agroportal.lirmm.fr/ontologies/EO/classes/http%3A%2F%2Fpurl.obolibrary.org%2Fobo%2FCHEBI_26872",
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"@context": {- "self": "http://www.w3.org/2002/07/owl#Class",
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{- "prefLabel": "humectant",
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"synonym": [],-
"definition": [- "A compound that is used to keep a substance moist."
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"synonym": [- "5-bromopyrimidine-2,4(1H,3H)-dione"
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"definition": [- "A pyrimidine having keto groups at the 2- and 4-positions and a bromo group at the 5-position. Used mainly as an experimental mutagen."
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{- "prefLabel": "urea exposure",
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"synonym": [- "urea treatment (narrow)"
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"definition": [- "Treatment involving the use of urea as source of nitrogen supplement to study various types of responses."
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"@context": {- "self": "http://www.w3.org/2002/07/owl#Class",
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{- "prefLabel": "chlorophenoxyacetic acid",
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"synonym": [- "chlorophenoxyacetic acids"
],-
"definition": [- "A monocarboxylic acid that is phenoxyacetic acid in which at least one of the phenyl hydrogens is replaced by chlorine."
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"links": {- "self": "https://data.agroportal.lirmm.fr/ontologies/EO/classes/http%3A%2F%2Fpurl.obolibrary.org%2Fobo%2FCHEBI_23152",
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"@context": {- "self": "http://www.w3.org/2002/07/owl#Class",
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{- "prefLabel": "lithium atom",
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"synonym": [],- "obsolete": false,
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"@context": {- "self": "http://www.w3.org/2002/07/owl#Class",
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{- "prefLabel": "cobalt atom",
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"synonym": [],-
"definition": [- "A cobalt group element atom that has atomic number 27."
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}
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{- "prefLabel": "ammonium nitrate exposure",
-
"synonym": [- "ammonium nitrate treatment (narrow)"
],-
"definition": [- "Treatment involving the use of ammonium nitrate supplement to study various types of responses."
],- "obsolete": false,
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"synonym": [- "muriate of potash exposure (related)"
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{- "prefLabel": "alicyclic compound",
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"synonym": [],-
"definition": [- "An aliphatic compound having a carbocyclic ring structure which may be saturated or unsaturated, but may not be a benzenoid or other aromatic system."
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"synonym": [],-
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{- "prefLabel": "carboxamide",
-
"synonym": [],-
"definition": [- "An amide of a carboxylic acid, having the structure RC(=O)NR2. The term is used as a suffix in systematic name formation to denote the -C(=O)NH2 group including its carbon atom."
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{- "prefLabel": "cupric sulfate exposure",
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"synonym": [- "cupric sulfate treatment (narrow)"
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"definition": [- "The treatment involving use of cupric sulfate for mutagenesis process."
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{- "prefLabel": "N-acetyl-D-aspartate(2-)",
-
"synonym": [- "N-acetyl-D-Asp",
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],-
"definition": [- "An N-acyl-D-alpha-amino acid anion resulting from deprotonation of both carboxy groups of N-acetyl-D-aspartic acid. Major microspecies at pH 7.3."
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