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PubMed:17059986 / 0-288 JSONTXT

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LitCoin-sentences

Id Subject Object Predicate Lexical cue
T1 0-112 Sentence denotes A novel splicing mutation in SLC12A3 associated with Gitelman syndrome and idiopathic intracranial hypertension.

LitCoin-entities

Id Subject Object Predicate Lexical cue db_id
3530 29-36 GeneOrGeneProduct denotes SLC12A3 NCBIGene:6559
3531 53-70 DiseaseOrPhenotypicFeature denotes Gitelman syndrome MESH:D053579
3532 75-111 DiseaseOrPhenotypicFeature denotes idiopathic intracranial hypertension MESH:D011559
3533 133-150 DiseaseOrPhenotypicFeature denotes Gitelman syndrome MESH:D053579
3534 152-154 DiseaseOrPhenotypicFeature denotes GS MESH:D053579
3535 214-226 DiseaseOrPhenotypicFeature denotes growth delay MESH:D006130
3536 228-247 DiseaseOrPhenotypicFeature denotes metabolic alkalosis MESH:D000471
3537 249-263 DiseaseOrPhenotypicFeature denotes hypomagnesemia MESH:C537153
3538 268-279 DiseaseOrPhenotypicFeature denotes hypokalemia MESH:D007008

LitCoin_Mondo

Id Subject Object Predicate Lexical cue mondo_id
T1 53-70 DiseaseOrPhenotypicFeature denotes Gitelman syndrome 0009904
T2 75-85 DiseaseOrPhenotypicFeature denotes idiopathic 0700005
T3 86-111 DiseaseOrPhenotypicFeature denotes intracranial hypertension 0006810
T4 133-150 DiseaseOrPhenotypicFeature denotes Gitelman syndrome 0009904

LitCoin-GeneOrGeneProduct-v2

Id Subject Object Predicate Lexical cue
T1 2-7 GeneOrGeneProduct denotes novel
T2 29-36 GeneOrGeneProduct denotes SLC12A3
T3 62-70 GeneOrGeneProduct denotes syndrome
T4 99-111 GeneOrGeneProduct denotes hypertension
T5 142-150 GeneOrGeneProduct denotes syndrome
T6 171-175 GeneOrGeneProduct denotes twin
T7 214-220 GeneOrGeneProduct denotes growth

LitCoin-GeneOrGeneProduct-v0

Id Subject Object Predicate Lexical cue
T1 2-7 GeneOrGeneProduct denotes novel
T2 8-16 GeneOrGeneProduct denotes splicing
T3 17-25 GeneOrGeneProduct denotes mutation
T4 29-36 GeneOrGeneProduct denotes SLC12A3
T5 62-70 GeneOrGeneProduct denotes syndrome
T6 99-111 GeneOrGeneProduct denotes hypertension
T7 125-129 GeneOrGeneProduct denotes case
T8 142-150 GeneOrGeneProduct denotes syndrome
T9 152-154 GeneOrGeneProduct denotes GS
T10 156-160 GeneOrGeneProduct denotes in a
T11 171-175 GeneOrGeneProduct denotes twin
T12 196-201 GeneOrGeneProduct denotes years
T13 214-220 GeneOrGeneProduct denotes growth

LitCoin-Disease-MeSH

Id Subject Object Predicate Lexical cue originalLabel
T1 53-70 DiseaseOrPhenotypicFeature denotes Gitelman syndrome D053579
T2 75-111 DiseaseOrPhenotypicFeature denotes idiopathic intracranial hypertension D011559
T3 133-150 DiseaseOrPhenotypicFeature denotes Gitelman syndrome D053579
T4 152-154 DiseaseOrPhenotypicFeature denotes GS D053579
T5 238-247 DiseaseOrPhenotypicFeature denotes alkalosis D000471
T6 268-279 DiseaseOrPhenotypicFeature denotes hypokalemia D007008

LitCoin-GeneOrGeneProduct-v3

Id Subject Object Predicate Lexical cue
T1 29-36 GeneOrGeneProduct denotes SLC12A3

LitCoin_Mondo_095

Id Subject Object Predicate Lexical cue mondo_id
T1 53-70 DiseaseOrPhenotypicFeature denotes Gitelman syndrome 0009904
T2 75-111 DiseaseOrPhenotypicFeature denotes idiopathic intracranial hypertension 0009468
T3 133-150 DiseaseOrPhenotypicFeature denotes Gitelman syndrome 0009904
T4 152-154 DiseaseOrPhenotypicFeature denotes GS 0005773|0009904
T6 249-263 DiseaseOrPhenotypicFeature denotes hypomagnesemia 0018100
T7 268-279 DiseaseOrPhenotypicFeature denotes hypokalemia 0003019

LitCoin-MeSH-Disease-2

Id Subject Object Predicate Lexical cue ID:
T1 53-70 DiseaseOrPhenotypicFeature denotes Gitelman syndrome D053579
T2 75-111 DiseaseOrPhenotypicFeature denotes idiopathic intracranial hypertension D011559
T3 133-150 DiseaseOrPhenotypicFeature denotes Gitelman syndrome D053579
T4 152-154 DiseaseOrPhenotypicFeature denotes GS D053579
T5 214-226 DiseaseOrPhenotypicFeature denotes growth delay DISEASE
T6 238-247 DiseaseOrPhenotypicFeature denotes alkalosis D000471
T7 249-263 DiseaseOrPhenotypicFeature denotes hypomagnesemia DISEASE
T8 268-279 DiseaseOrPhenotypicFeature denotes hypokalemia D007008

LitCoin-MONDO_bioort2019

Id Subject Object Predicate Lexical cue #label
T1 53-70 DiseaseOrPhenotypicFeature denotes Gitelman syndrome D053579
T2 75-111 DiseaseOrPhenotypicFeature denotes idiopathic intracranial hypertension D011559
T3 133-150 DiseaseOrPhenotypicFeature denotes Gitelman syndrome D053579
T4 152-154 DiseaseOrPhenotypicFeature denotes GS D053579
T5 214-226 DiseaseOrPhenotypicFeature denotes growth delay DISEASE
T6 238-247 DiseaseOrPhenotypicFeature denotes alkalosis D000471
T7 249-263 DiseaseOrPhenotypicFeature denotes hypomagnesemia DISEASE
T8 268-279 DiseaseOrPhenotypicFeature denotes hypokalemia D007008

LitCoin-training-merged

Id Subject Object Predicate Lexical cue #label
T21958 29-36 GeneOrGeneProduct denotes SLC12A3
T8 268-279 DiseaseOrPhenotypicFeature denotes hypokalemia D007008
T53492 249-263 DiseaseOrPhenotypicFeature denotes hypomagnesemia DISEASE
T6 238-247 DiseaseOrPhenotypicFeature denotes alkalosis D000471
T41383 214-226 DiseaseOrPhenotypicFeature denotes growth delay DISEASE
T4 152-154 DiseaseOrPhenotypicFeature denotes GS D053579
T75669 133-150 DiseaseOrPhenotypicFeature denotes Gitelman syndrome D053579
T63087 75-111 DiseaseOrPhenotypicFeature denotes idiopathic intracranial hypertension D011559
T73539 53-70 DiseaseOrPhenotypicFeature denotes Gitelman syndrome D053579

sentences

Id Subject Object Predicate Lexical cue
TextSentencer_T1 0-112 Sentence denotes A novel splicing mutation in SLC12A3 associated with Gitelman syndrome and idiopathic intracranial hypertension.
T1 0-112 Sentence denotes A novel splicing mutation in SLC12A3 associated with Gitelman syndrome and idiopathic intracranial hypertension.

DisGeNET

Id Subject Object Predicate Lexical cue
T0 29-36 gene:6559 denotes SLC12A3
T1 53-70 disease:C0268450 denotes Gitelman syndrome
T2 29-36 gene:6559 denotes SLC12A3
T3 75-111 disease:C0033845 denotes idiopathic intracranial hypertension
R1 T0 T1 associated_with SLC12A3,Gitelman syndrome
R2 T2 T3 associated_with SLC12A3,idiopathic intracranial hypertension

PubmedHPO

Id Subject Object Predicate Lexical cue
T1 214-226 HP_0001510 denotes growth delay
T2 228-247 HP_0200114 denotes metabolic alkalosis
T3 238-247 HP_0001948 denotes alkalosis
T4 249-263 HP_0002917 denotes hypomagnesemia
T5 268-279 HP_0002900 denotes hypokalemia

DisGeNET5_gene_disease

Id Subject Object Predicate Lexical cue
17059986-0#29#36#gene6559 29-36 gene6559 denotes SLC12A3
17059986-0#53#70#diseaseC0268450 53-70 diseaseC0268450 denotes Gitelman syndrome
17059986-0#75#111#diseaseC0033845 75-111 diseaseC0033845 denotes idiopathic intracranial hypertension
29#36#gene655953#70#diseaseC0268450 17059986-0#29#36#gene6559 17059986-0#53#70#diseaseC0268450 associated_with SLC12A3,Gitelman syndrome
29#36#gene655975#111#diseaseC0033845 17059986-0#29#36#gene6559 17059986-0#75#111#diseaseC0033845 associated_with SLC12A3,idiopathic intracranial hypertension

PubCasesHPO

Id Subject Object Predicate Lexical cue
TI1 99-111 HP:0000822 denotes hypertension
AB1 214-226 HP:0001510 denotes growth delay
AB2 228-247 HP:0200114 denotes metabolic alkalosis
AB3 249-263 HP:0002917 denotes hypomagnesemia
AB4 268-279 HP:0002900 denotes hypokalemia

PubCasesORDO

Id Subject Object Predicate Lexical cue
AB1 133-150 ORDO:358 denotes Gitelman syndrome
TI1 53-70 ORDO:358 denotes Gitelman syndrome
TI2 75-111 ORDO:238624 denotes idiopathic intracranial hypertension