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PubMed:15951966 / 81-284 JSONTXT

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LitCoin-sentences

Id Subject Object Predicate Lexical cue
T3 0-203 Sentence denotes Exonic deletions in MSH2 and MLH1 are significant contributors to the mutation spectrum in HNPCC, and heterozygous changes in exon copy number are not detected by conventional mutation screening methods.

LitCoin-entities

Id Subject Object Predicate Lexical cue db_id
1946 20-24 GeneOrGeneProduct denotes MSH2 NCBIGene:4436
1947 29-33 GeneOrGeneProduct denotes MLH1 NCBIGene:4292
1948 91-96 DiseaseOrPhenotypicFeature denotes HNPCC MESH:D003123

LitCoin-GeneOrGeneProduct-v0

Id Subject Object Predicate Lexical cue
T4 20-24 GeneOrGeneProduct denotes MSH2
T5 29-33 GeneOrGeneProduct denotes MLH1
T6 70-78 GeneOrGeneProduct denotes mutation
T7 91-96 GeneOrGeneProduct denotes HNPCC
T8 176-184 GeneOrGeneProduct denotes mutation
T9 195-202 GeneOrGeneProduct denotes methods

LitCoin-GeneOrGeneProduct-v2

Id Subject Object Predicate Lexical cue
T3 20-24 GeneOrGeneProduct denotes MSH2
T4 29-33 GeneOrGeneProduct denotes MLH1
T5 91-96 GeneOrGeneProduct denotes HNPCC

LitCoin-Disease-MeSH

Id Subject Object Predicate Lexical cue originalLabel
T1 91-96 DiseaseOrPhenotypicFeature denotes HNPCC DISEASE

LitCoin-GeneOrGeneProduct-v3

Id Subject Object Predicate Lexical cue
T3 20-24 GeneOrGeneProduct denotes MSH2
T4 29-33 GeneOrGeneProduct denotes MLH1

LitCoin_Mondo_095

Id Subject Object Predicate Lexical cue mondo_id
T1 91-96 DiseaseOrPhenotypicFeature denotes HNPCC 0018630

LitCoin-MeSH-Disease-2

Id Subject Object Predicate Lexical cue ID:
T1 91-96 DiseaseOrPhenotypicFeature denotes HNPCC DISEASE

LitCoin-MONDO_bioort2019

Id Subject Object Predicate Lexical cue #label
T1 91-96 DiseaseOrPhenotypicFeature denotes HNPCC DISEASE

LitCoin-training-merged

Id Subject Object Predicate Lexical cue #label
T4 29-33 GeneOrGeneProduct denotes MLH1
T3 20-24 GeneOrGeneProduct denotes MSH2
T45079 91-96 DiseaseOrPhenotypicFeature denotes HNPCC DISEASE