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PubMed:10581255 JSONTXT

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ggdb-test

Id Subject Object Predicate Lexical cue
T1 1053-1057 https://acgg.asia/db/ggdb/info/gg144 denotes ALG3

PMID_GLOBAL

Id Subject Object Predicate Lexical cue mondo_id
T1 0-52 DiseaseOrPhenotypicFeature denotes Carbohydrate deficient glycoprotein syndrome type IV 0010998
T2 147-192 DiseaseOrPhenotypicFeature denotes carbohydrate deficient glycoprotein syndromes 0015286
T3 194-198 DiseaseOrPhenotypicFeature denotes CDGS 0015286
T4 220-232 DiseaseOrPhenotypicFeature denotes microcephaly 0001149
T5 241-249 DiseaseOrPhenotypicFeature denotes epilepsy 0005027
T6 378-384 DiseaseOrPhenotypicFeature denotes defect 0008568
T7 620-626 DiseaseOrPhenotypicFeature denotes defect 0008568

GGDB-2020

Id Subject Object Predicate Lexical cue
T1 1053-1057 https://acgg.asia/db/ggdb/info/gg144 denotes ALG3

PubmedHPO

Id Subject Object Predicate Lexical cue
T1 220-232 HP_0000252 denotes microcephaly

glycogenes

Id Subject Object Predicate Lexical cue
PD-GlycoGenes20190927-B_T1 1053-1057 https://acgg.asia/db/ggdb/info/gg144 denotes ALG3

NGLY1-deficiency

Id Subject Object Predicate Lexical cue
PD-NGLY1-deficiency-B_T1 89-95 chem:24139 denotes GlcNAc
PD-NGLY1-deficiency-B_T2 593-599 chem:24139 denotes GlcNAc