PubMed:17959715 / 1663-2021 JSONTXT

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LitCoin-entities

Id Subject Object Predicate Lexical cue db_id
4483 4-8 GeneOrGeneProduct denotes MLH1 NCBIGene:4292
4484 59-62 DiseaseOrPhenotypicFeature denotes AML MESH:D015470
4485 94-97 DiseaseOrPhenotypicFeature denotes AML MESH:D015470
4486 231-234 DiseaseOrPhenotypicFeature denotes AML MESH:D015470
4487 305-313 OrganismTaxon denotes patients NCBITaxon:9606

LitCoin-sentences

Id Subject Object Predicate Lexical cue
T12 0-358 Sentence denotes The MLH1 -93 variant allele was also over-represented in t-AML cases when compared to de novo AML cases (36.9%, n = 420) and healthy controls (36.3%, n = 952), and was associated with a significantly increased risk of developing t-AML (odds ratio 5.31, 95% confidence interval 1.40 to 20.15), but only in patients previously treated with a methylating agent.

LitCoin-GeneOrGeneProduct-v0

Id Subject Object Predicate Lexical cue
T25 4-8 GeneOrGeneProduct denotes MLH1
T26 57-62 GeneOrGeneProduct denotes t-AML
T27 63-68 GeneOrGeneProduct denotes cases
T28 98-103 GeneOrGeneProduct denotes cases
T29 154-157 GeneOrGeneProduct denotes 952
T30 229-234 GeneOrGeneProduct denotes t-AML

LitCoin-GeneOrGeneProduct-v2

Id Subject Object Predicate Lexical cue
T14 4-8 GeneOrGeneProduct denotes MLH1
T15 154-157 GeneOrGeneProduct denotes 952

LitCoin-GeneOrGeneProduct-v3

Id Subject Object Predicate Lexical cue
T8 4-8 GeneOrGeneProduct denotes MLH1
T9 154-157 GeneOrGeneProduct denotes 952

LitCoin_Mondo_095

Id Subject Object Predicate Lexical cue mondo_id
T11 59-62 DiseaseOrPhenotypicFeature denotes AML 0018874
T12 94-97 DiseaseOrPhenotypicFeature denotes AML 0018874
T13 231-234 DiseaseOrPhenotypicFeature denotes AML 0018874

LitCoin-MeSH-Disease-2

Id Subject Object Predicate Lexical cue ID:
T18 59-62 DiseaseOrPhenotypicFeature denotes AML DISEASE
T19 94-97 DiseaseOrPhenotypicFeature denotes AML DISEASE
T20 231-234 DiseaseOrPhenotypicFeature denotes AML DISEASE

LitCoin-MONDO_bioort2019

Id Subject Object Predicate Lexical cue #label
T18 59-62 DiseaseOrPhenotypicFeature denotes AML DISEASE
T19 94-97 DiseaseOrPhenotypicFeature denotes AML DISEASE
T20 231-234 DiseaseOrPhenotypicFeature denotes AML DISEASE

LitCoin-NCBITaxon-2

Id Subject Object Predicate Lexical cue
T7 305-313 OrganismTaxon denotes patients

LitCoin-training-merged

Id Subject Object Predicate Lexical cue #label
T9 154-157 GeneOrGeneProduct denotes 952
T8 4-8 GeneOrGeneProduct denotes MLH1
T20 231-234 DiseaseOrPhenotypicFeature denotes AML DISEASE
T19 94-97 DiseaseOrPhenotypicFeature denotes AML DISEASE
T18 59-62 DiseaseOrPhenotypicFeature denotes AML DISEASE
T80947 305-313 OrganismTaxon denotes patients

PMID_GLOBAL

Id Subject Object Predicate Lexical cue mondo_id
T11 59-62 DiseaseOrPhenotypicFeature denotes AML 0018874
T12 94-97 DiseaseOrPhenotypicFeature denotes AML 0018874
T13 231-234 DiseaseOrPhenotypicFeature denotes AML 0018874