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PubMed:18366737 / 453-625 JSONTXT

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PMID_GLOBAL

Id Subject Object Predicate Lexical cue mondo_id
T8 22-31 DiseaseOrPhenotypicFeature denotes Leiomyoma 0001572
T9 89-91 DiseaseOrPhenotypicFeature denotes FH 0016525
T10 109-150 DiseaseOrPhenotypicFeature denotes multiple cutaneous and uterine leiomyomas 0007888
T11 153-157 DiseaseOrPhenotypicFeature denotes MCUL 0007888

LitCoin-sentences

Id Subject Object Predicate Lexical cue
T5 0-172 Sentence denotes In 2002, the Multiple Leiomyoma Consortium identified heterozygous germline mutations of FH in patients with multiple cutaneous and uterine leiomyomas, (MCUL: OMIM 150800).

LitCoin-entities

Id Subject Object Predicate Lexical cue db_id
4846 22-31 DiseaseOrPhenotypicFeature denotes Leiomyoma MESH:D007889
4847 89-91 GeneOrGeneProduct denotes FH NCBIGene:2271
4848 95-103 OrganismTaxon denotes patients NCBITaxon:9606
4849 109-150 DiseaseOrPhenotypicFeature denotes multiple cutaneous and uterine leiomyomas MESH:C535516
4850 153-157 DiseaseOrPhenotypicFeature denotes MCUL MESH:C535516
4851 159-170 DiseaseOrPhenotypicFeature denotes OMIM 150800 MESH:C535516

LitCoin_Mondo

Id Subject Object Predicate Lexical cue mondo_id
T2 22-31 DiseaseOrPhenotypicFeature denotes Leiomyoma 0001572
T3 140-150 DiseaseOrPhenotypicFeature denotes leiomyomas 0001572

LitCoin-GeneOrGeneProduct-v2

Id Subject Object Predicate Lexical cue
T12 13-21 GeneOrGeneProduct denotes Multiple
T13 109-117 GeneOrGeneProduct denotes multiple

LitCoin-GeneOrGeneProduct-v0

Id Subject Object Predicate Lexical cue
T17 13-21 GeneOrGeneProduct denotes Multiple
T18 76-85 GeneOrGeneProduct denotes mutations
T19 109-117 GeneOrGeneProduct denotes multiple
T20 153-157 GeneOrGeneProduct denotes MCUL

LitCoin-Disease-MeSH

Id Subject Object Predicate Lexical cue originalLabel
T5 22-31 DiseaseOrPhenotypicFeature denotes Leiomyoma D007889
T6 140-150 DiseaseOrPhenotypicFeature denotes leiomyomas D007889

LitCoin_Mondo_095

Id Subject Object Predicate Lexical cue mondo_id
T8 22-31 DiseaseOrPhenotypicFeature denotes Leiomyoma 0001572
T9 89-91 DiseaseOrPhenotypicFeature denotes FH 0016525
T10 109-150 DiseaseOrPhenotypicFeature denotes multiple cutaneous and uterine leiomyomas 0007888
T11 153-157 DiseaseOrPhenotypicFeature denotes MCUL 0007888

LitCoin-MeSH-Disease-2

Id Subject Object Predicate Lexical cue ID:
T8 22-31 DiseaseOrPhenotypicFeature denotes Leiomyoma D007889
T9 109-150 DiseaseOrPhenotypicFeature denotes multiple cutaneous and uterine leiomyomas DISEASE
T10 153-157 DiseaseOrPhenotypicFeature denotes MCUL DISEASE
T11 159-170 DiseaseOrPhenotypicFeature denotes OMIM 150800 DISEASE

LitCoin-MONDO_bioort2019

Id Subject Object Predicate Lexical cue #label
T7 22-31 DiseaseOrPhenotypicFeature denotes Leiomyoma D007889
T8 109-150 DiseaseOrPhenotypicFeature denotes multiple cutaneous and uterine leiomyomas DISEASE
T9 153-157 DiseaseOrPhenotypicFeature denotes MCUL DISEASE
T10 159-170 DiseaseOrPhenotypicFeature denotes OMIM 150800 DISEASE

LitCoin-NCBITaxon-2

Id Subject Object Predicate Lexical cue
T1 95-103 OrganismTaxon denotes patients

LitCoin-training-merged

Id Subject Object Predicate Lexical cue #label
T30897 159-170 DiseaseOrPhenotypicFeature denotes OMIM 150800 DISEASE
T77092 153-157 DiseaseOrPhenotypicFeature denotes MCUL DISEASE
T43739 109-150 DiseaseOrPhenotypicFeature denotes multiple cutaneous and uterine leiomyomas DISEASE
T50201 22-31 DiseaseOrPhenotypicFeature denotes Leiomyoma D007889
T73931 95-103 OrganismTaxon denotes patients