loading...| Preferred Name |
observed_variation |
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| Synonyms |
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| Definitions |
It is the variation (of nucleotides or of residues) observed between the 2 patients (reference sequence and the alternative sequence - if it's possible to talk about a "reference") when a genomic variation is described. Ex: A>C, CT>A, Ser>Thr, etc. |
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| ID |
http://www.loria.fr/~coulet/ontology/snpontology/version1.6/snpontology_full.owl#observed_variation |
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| comment |
It is the variation (of nucleotides or of residues) observed between the 2 patients (reference sequence and the alternative sequence - if it's possible to talk about a "reference") when a genomic variation is described. Ex: A>C, CT>A, Ser>Thr, etc. |
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| prefixIRI |
SNPO:observed_variation |
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| prefLabel |
observed_variation |
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| disjointWith |
http://www.loria.fr/~coulet/ontology/snpontology/version1.6/snpontology_full.owl#sequence_position http://www.loria.fr/~coulet/ontology/snpontology/version1.6/snpontology_full.owl#sequence http://www.loria.fr/~coulet/ontology/snpontology/version1.6/snpontology_full.owl#variant |
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| subClassOf |