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PMC:7291971 / 14382-14572 JSONTXT

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LitCovid-PMC-OGER-BB

Id Subject Object Predicate Lexical cue
T333 44-52 CHEBI:36357;CHEBI:36357 denotes compound
T334 87-95 CHEBI:17478;CHEBI:17478 denotes aldehyde
T335 148-152 CHEBI:41865;CHEBI:41865 denotes acid

LitCovid-PD-FMA-UBERON

Id Subject Object Predicate Lexical cue fma_id
T55 139-152 Body_part denotes aspartic acid http://purl.org/sig/ont/fma/fma82760

LitCovid-PubTator

Id Subject Object Predicate Lexical cue tao:has_database_id
301 87-95 Chemical denotes aldehyde MESH:D000447
302 137-152 Chemical denotes l-aspartic acid MESH:D001224

LitCovid-PD-CLO

Id Subject Object Predicate Lexical cue
T130 163-164 http://purl.obolibrary.org/obo/CLO_0001020 denotes a

LitCovid-PD-CHEBI

Id Subject Object Predicate Lexical cue chebi_id
T244 87-95 Chemical denotes aldehyde http://purl.obolibrary.org/obo/CHEBI_17478
T245 139-152 Chemical denotes aspartic acid http://purl.obolibrary.org/obo/CHEBI_22660
T246 148-152 Chemical denotes acid http://purl.obolibrary.org/obo/CHEBI_37527

2_test

Id Subject Object Predicate Lexical cue
32563813-28823155-29105578 186-188 28823155 denotes 25

LitCovid-sentences

Id Subject Object Predicate Lexical cue
T88 0-190 Sentence denotes Compounds 2, 3 and 4 were obtained from key compound 20 via reductive amination of the aldehyde 21 that was prepared in three steps from l-aspartic acid following a published procedure [25].

MyTest

Id Subject Object Predicate Lexical cue
32563813-28823155-29105578 186-188 28823155 denotes 25