> top > docs > PubMed:15000256 > spans > 0-165 > annotations

PubMed:15000256 / 0-165 JSONTXT

Annnotations TAB JSON ListView MergeView

LitCoin-entities

Id Subject Object Predicate Lexical cue db_id
524 56-60 GeneOrGeneProduct denotes FMR1 NCBIGene:2332
525 69-77 DiseaseOrPhenotypicFeature denotes autistic MESH:D001321
526 82-99 DiseaseOrPhenotypicFeature denotes mentally retarded MESH:D008607
527 119-137 DiseaseOrPhenotypicFeature denotes Fragile X syndrome MESH:D005600

LitCoin-sentences

Id Subject Object Predicate Lexical cue
T1 0-118 Sentence denotes Single-strand conformation polymorphism analysis of the FMR1 gene in autistic and mentally retarded children in Japan.

LitCoin_Mondo

Id Subject Object Predicate Lexical cue mondo_id
T1 119-137 DiseaseOrPhenotypicFeature denotes Fragile X syndrome 0010383

LitCoin-GeneOrGeneProduct-v0

Id Subject Object Predicate Lexical cue
T1 7-13 GeneOrGeneProduct denotes strand
T2 56-60 GeneOrGeneProduct denotes FMR1
T3 119-128 GeneOrGeneProduct denotes Fragile X
T4 129-137 GeneOrGeneProduct denotes syndrome

LitCoin-GeneOrGeneProduct-v2

Id Subject Object Predicate Lexical cue
T1 56-60 GeneOrGeneProduct denotes FMR1
T2 119-128 GeneOrGeneProduct denotes Fragile X
T3 129-137 GeneOrGeneProduct denotes syndrome

LitCoin-Disease-MeSH

Id Subject Object Predicate Lexical cue originalLabel
T1 119-137 DiseaseOrPhenotypicFeature denotes Fragile X syndrome D005600

LitCoin-GeneOrGeneProduct-v3

Id Subject Object Predicate Lexical cue
T1 56-60 GeneOrGeneProduct denotes FMR1
T2 119-128 GeneOrGeneProduct denotes Fragile X

LitCoin_Mondo_095

Id Subject Object Predicate Lexical cue mondo_id
T1 119-137 DiseaseOrPhenotypicFeature denotes Fragile X syndrome 0010383

LitCoin-MeSH-Disease-2

Id Subject Object Predicate Lexical cue ID:
T1 69-77 DiseaseOrPhenotypicFeature denotes autistic DISEASE
T2 82-99 DiseaseOrPhenotypicFeature denotes mentally retarded DISEASE
T3 119-137 DiseaseOrPhenotypicFeature denotes Fragile X syndrome D005600

LitCoin-MONDO_bioort2019

Id Subject Object Predicate Lexical cue #label
T1 69-77 DiseaseOrPhenotypicFeature denotes autistic DISEASE
T2 82-99 DiseaseOrPhenotypicFeature denotes mentally retarded DISEASE
T3 119-137 DiseaseOrPhenotypicFeature denotes Fragile X syndrome D005600

LitCoin-training-merged

Id Subject Object Predicate Lexical cue #label
T2 119-128 GeneOrGeneProduct denotes Fragile X
T1 56-60 GeneOrGeneProduct denotes FMR1
T42164 119-137 DiseaseOrPhenotypicFeature denotes Fragile X syndrome D005600
T37013 82-99 DiseaseOrPhenotypicFeature denotes mentally retarded DISEASE
T50736 69-77 DiseaseOrPhenotypicFeature denotes autistic DISEASE

DisGeNET5_gene_disease

Id Subject Object Predicate Lexical cue
15000256-0#56#60#gene2332 56-60 gene2332 denotes FMR1
15000256-0#69#77#diseaseC0004352 69-77 diseaseC0004352 denotes autistic
56#60#gene233269#77#diseaseC0004352 15000256-0#56#60#gene2332 15000256-0#69#77#diseaseC0004352 associated_with FMR1,autistic