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PubMed:27930654 / 279-507 JSONTXT

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LitCoin-entities

Id Subject Object Predicate Lexical cue db_id
11796 34-59 DiseaseOrPhenotypicFeature denotes inherited human disorders MESH:D030342
11797 61-73 DiseaseOrPhenotypicFeature denotes ciliopathies MESH:D000072661
11798 83-103 DiseaseOrPhenotypicFeature denotes retinitis pigmentosa MESH:D012174
11799 108-129 DiseaseOrPhenotypicFeature denotes Bardet-Biedl syndrome MESH:D020788
11800 131-134 DiseaseOrPhenotypicFeature denotes BBS MESH:D020788

LitCoin-sentences

Id Subject Object Predicate Lexical cue
T3 0-228 Sentence denotes Defects in these organelles cause inherited human disorders (ciliopathies) such as retinitis pigmentosa and Bardet-Biedl syndrome (BBS), frequently affecting many physiological and developmental processes across multiple organs.

LitCoin-entities-OrganismTaxon-PD

Id Subject Object Predicate Lexical cue db_id
T1 44-49 OrganismTaxon denotes human NCBItxid:9606

LitCoin_Mondo

Id Subject Object Predicate Lexical cue mondo_id
T1 34-43 DiseaseOrPhenotypicFeature denotes inherited 0021152
T2 61-73 DiseaseOrPhenotypicFeature denotes ciliopathies 0005308
T3 83-103 DiseaseOrPhenotypicFeature denotes retinitis pigmentosa 0019200
T4 83-92 DiseaseOrPhenotypicFeature denotes retinitis 0002708
T5 108-129 DiseaseOrPhenotypicFeature denotes Bardet-Biedl syndrome 0015229

LitCoin-GeneOrGeneProduct-v0

Id Subject Object Predicate Lexical cue
T9 0-7 GeneOrGeneProduct denotes Defects
T10 83-92 GeneOrGeneProduct denotes retinitis
T11 121-129 GeneOrGeneProduct denotes syndrome
T12 158-162 GeneOrGeneProduct denotes many
T13 195-204 GeneOrGeneProduct denotes processes
T14 212-220 GeneOrGeneProduct denotes multiple

LitCoin-GeneOrGeneProduct-v2

Id Subject Object Predicate Lexical cue
T7 121-129 GeneOrGeneProduct denotes syndrome
T8 212-220 GeneOrGeneProduct denotes multiple

LitCoin-NCBITaxon-2

Id Subject Object Predicate Lexical cue
T1 44-49 OrganismTaxon denotes human

LitCoin-Disease-MeSH

Id Subject Object Predicate Lexical cue originalLabel
T1 61-73 DiseaseOrPhenotypicFeature denotes ciliopathies D000072661
T2 83-103 DiseaseOrPhenotypicFeature denotes retinitis pigmentosa D012174
T3 108-129 DiseaseOrPhenotypicFeature denotes Bardet-Biedl syndrome D020788
T4 131-134 DiseaseOrPhenotypicFeature denotes BBS D020788

LitCoin_Mondo_095

Id Subject Object Predicate Lexical cue mondo_id
T1 61-73 DiseaseOrPhenotypicFeature denotes ciliopathies 0005308
T2 83-103 DiseaseOrPhenotypicFeature denotes retinitis pigmentosa 0019200|0008377
T4 108-129 DiseaseOrPhenotypicFeature denotes Bardet-Biedl syndrome 0015229|0014432
T6 131-134 DiseaseOrPhenotypicFeature denotes BBS 0015229|0014432

LitCoin-MeSH-Disease-2

Id Subject Object Predicate Lexical cue ID:
T1 34-59 DiseaseOrPhenotypicFeature denotes inherited human disorders DISEASE
T2 61-73 DiseaseOrPhenotypicFeature denotes ciliopathies D000072661
T3 83-103 DiseaseOrPhenotypicFeature denotes retinitis pigmentosa D012174
T4 108-129 DiseaseOrPhenotypicFeature denotes Bardet-Biedl syndrome D020788
T5 131-134 DiseaseOrPhenotypicFeature denotes BBS D020788

LitCoin-MONDO_bioort2019

Id Subject Object Predicate Lexical cue #label
T1 34-59 DiseaseOrPhenotypicFeature denotes inherited human disorders DISEASE
T2 61-73 DiseaseOrPhenotypicFeature denotes ciliopathies D000072661
T3 83-103 DiseaseOrPhenotypicFeature denotes retinitis pigmentosa D012174
T4 108-129 DiseaseOrPhenotypicFeature denotes Bardet-Biedl syndrome D020788
T5 131-134 DiseaseOrPhenotypicFeature denotes BBS D020788

LitCoin-training-merged

Id Subject Object Predicate Lexical cue #label
T15507 131-134 DiseaseOrPhenotypicFeature denotes BBS D020788
T56269 108-129 DiseaseOrPhenotypicFeature denotes Bardet-Biedl syndrome D020788
T57409 83-103 DiseaseOrPhenotypicFeature denotes retinitis pigmentosa D012174
T71830 61-73 DiseaseOrPhenotypicFeature denotes ciliopathies D000072661
T68457 34-59 DiseaseOrPhenotypicFeature denotes inherited human disorders DISEASE
T45910 44-49 OrganismTaxon denotes human