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PubMed:17549393 / 347-444 JSONTXT

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LitCoin-entities

Id Subject Object Predicate Lexical cue db_id
4130 0-3 DiseaseOrPhenotypicFeature denotes VWS MESH:C536528
4131 59-89 GeneOrGeneProduct denotes interferon regulatory factor 6 NCBIGene:3664
4132 91-95 GeneOrGeneProduct denotes IRF6 NCBIGene:3664

LitCoin-sentences

Id Subject Object Predicate Lexical cue
T4 0-97 Sentence denotes VWS arises as the result of mutations in the gene encoding interferon regulatory factor 6 (IRF6).

LitCoin-GeneOrGeneProduct-v0

Id Subject Object Predicate Lexical cue
T19 25-37 GeneOrGeneProduct denotes of mutations
T20 59-89 GeneOrGeneProduct denotes interferon regulatory factor 6
T21 91-95 GeneOrGeneProduct denotes IRF6

LitCoin-GeneOrGeneProduct-v2

Id Subject Object Predicate Lexical cue
T10 59-89 GeneOrGeneProduct denotes interferon regulatory factor 6
T11 91-95 GeneOrGeneProduct denotes IRF6

LitCoin-Disease-MeSH

Id Subject Object Predicate Lexical cue originalLabel
T9 0-3 DiseaseOrPhenotypicFeature denotes VWS C536528

LitCoin-GeneOrGeneProduct-v3

Id Subject Object Predicate Lexical cue
T3 59-89 GeneOrGeneProduct denotes interferon regulatory factor 6
T4 91-95 GeneOrGeneProduct denotes IRF6

LitCoin_Mondo_095

Id Subject Object Predicate Lexical cue mondo_id
T10 0-3 DiseaseOrPhenotypicFeature denotes VWS 0019508

LitCoin-MeSH-Disease-2

Id Subject Object Predicate Lexical cue ID:
T9 0-3 DiseaseOrPhenotypicFeature denotes VWS C536528

LitCoin-MONDO_bioort2019

Id Subject Object Predicate Lexical cue #label
T9 0-3 DiseaseOrPhenotypicFeature denotes VWS C536528

LitCoin-training-merged

Id Subject Object Predicate Lexical cue #label
T4 91-95 GeneOrGeneProduct denotes IRF6
T3 59-89 GeneOrGeneProduct denotes interferon regulatory factor 6
T29463 0-3 DiseaseOrPhenotypicFeature denotes VWS C536528