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PubMed:1353340 / 159-187 JSONTXT

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LitCoin-entities

Id Subject Object Predicate Lexical cue db_id
3 0-28 DiseaseOrPhenotypicFeature denotes metachromatic leukodystrophy MESH:D007966

LitCoin_Mondo

Id Subject Object Predicate Lexical cue mondo_id
T3 0-28 DiseaseOrPhenotypicFeature denotes metachromatic leukodystrophy 0018868
T4 14-28 DiseaseOrPhenotypicFeature denotes leukodystrophy 0019046

LitCoin-Disease-MeSH

Id Subject Object Predicate Lexical cue originalLabel
T2 0-28 DiseaseOrPhenotypicFeature denotes metachromatic leukodystrophy D007966

LitCoin_Mondo_095

Id Subject Object Predicate Lexical cue mondo_id
T4 0-28 DiseaseOrPhenotypicFeature denotes metachromatic leukodystrophy 0018868|0009591

LitCoin-MeSH-Disease-2

Id Subject Object Predicate Lexical cue ID:
T2 0-28 DiseaseOrPhenotypicFeature denotes metachromatic leukodystrophy D007966

LitCoin-MONDO_bioort2019

Id Subject Object Predicate Lexical cue #label
T2 0-28 DiseaseOrPhenotypicFeature denotes metachromatic leukodystrophy D007966

LitCoin-training-merged

Id Subject Object Predicate Lexical cue #label
T87689 0-28 DiseaseOrPhenotypicFeature denotes metachromatic leukodystrophy D007966

PubCasesHPO

Id Subject Object Predicate Lexical cue
AB1 14-28 HP:0002415 denotes leukodystrophy

PubCasesORDO

Id Subject Object Predicate Lexical cue
AB1 0-28 ORDO:512 denotes metachromatic leukodystrophy

NCBIDiseaseCorpus

Id Subject Object Predicate Lexical cue
T2 0-28 SpecificDisease:D007966 denotes metachromatic leukodystrophy

DisGeNET

Id Subject Object Predicate Lexical cue
T3 0-28 disease:C0023522 denotes metachromatic leukodystrophy
T7 0-28 disease:C0023522 denotes metachromatic leukodystrophy