PubMed:19048115 / 1086-1213 JSONTXT

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LitCoin-sentences

Id Subject Object Predicate Lexical cue
T7 0-127 Sentence denotes Similarly, NF1 alterations including homozygous deletions and splicing mutations were identified in 9 (22%) of 41 primary OSCs.

LitCoin-entities

Id Subject Object Predicate Lexical cue db_id
5575 11-14 GeneOrGeneProduct denotes NF1 NCBIGene:4763
5576 122-126 DiseaseOrPhenotypicFeature denotes OSCs MESH:D010051

LitCoin-GeneOrGeneProduct-v0

Id Subject Object Predicate Lexical cue
T46 0-9 GeneOrGeneProduct denotes Similarly
T47 11-14 GeneOrGeneProduct denotes NF1
T48 62-70 GeneOrGeneProduct denotes splicing
T49 71-80 GeneOrGeneProduct denotes mutations
T50 97-101 GeneOrGeneProduct denotes in 9
T51 122-126 GeneOrGeneProduct denotes OSCs

LitCoin-GeneOrGeneProduct-v2

Id Subject Object Predicate Lexical cue
T28 11-14 GeneOrGeneProduct denotes NF1

LitCoin-GeneOrGeneProduct-v3

Id Subject Object Predicate Lexical cue
T15 11-14 GeneOrGeneProduct denotes NF1

LitCoin_Mondo_095

Id Subject Object Predicate Lexical cue mondo_id
T14 11-14 DiseaseOrPhenotypicFeature denotes NF1 0018975

LitCoin-MeSH-Disease-2

Id Subject Object Predicate Lexical cue ID:
T13 122-126 DiseaseOrPhenotypicFeature denotes OSCs DISEASE

LitCoin-MONDO_bioort2019

Id Subject Object Predicate Lexical cue #label
T12 122-126 DiseaseOrPhenotypicFeature denotes OSCs DISEASE

LitCoin-training-merged

Id Subject Object Predicate Lexical cue #label
T15 11-14 GeneOrGeneProduct denotes NF1
T95800 122-126 DiseaseOrPhenotypicFeature denotes OSCs DISEASE

PMID_GLOBAL

Id Subject Object Predicate Lexical cue mondo_id
T14 11-14 DiseaseOrPhenotypicFeature denotes NF1 0018975