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PubMed:16005363 / 0-99 JSON TXT

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LitCoin-sentences

Id	Subject	Object	Predicate	Lexical cue
T1	0-99	Sentence	denotes	Identification of a novel WFS1 mutation (AFF344-345ins) in Japanese patients with Wolfram syndrome.

LitCoin-entities

Id	Subject	Object	Predicate	Lexical cue	db_id
2045	26-30	GeneOrGeneProduct	denotes	WFS1	NCBIGene:7466
2046	41-54	SequenceVariant	denotes	AFF344-345ins	p\|INS\|344_345\|AFF
2047	68-76	OrganismTaxon	denotes	patients	NCBITaxon:9606
2048	82-98	DiseaseOrPhenotypicFeature	denotes	Wolfram syndrome	MESH:D014929

LitCoin_Mondo

Id	Subject	Object	Predicate	Lexical cue	mondo_id
T1	82-98	DiseaseOrPhenotypicFeature	denotes	Wolfram syndrome	0018105

LitCoin-GeneOrGeneProduct-v0

Id	Subject	Object	Predicate	Lexical cue
T1	20-25	GeneOrGeneProduct	denotes	novel
T2	26-30	GeneOrGeneProduct	denotes	WFS1
T3	31-39	GeneOrGeneProduct	denotes	mutation
T4	90-98	GeneOrGeneProduct	denotes	syndrome

LitCoin-GeneOrGeneProduct-v2

Id	Subject	Object	Predicate	Lexical cue
T1	20-25	GeneOrGeneProduct	denotes	novel
T2	26-30	GeneOrGeneProduct	denotes	WFS1
T3	90-98	GeneOrGeneProduct	denotes	syndrome

LitCoin-Disease-MeSH

Id	Subject	Object	Predicate	Lexical cue	originalLabel
T1	82-98	DiseaseOrPhenotypicFeature	denotes	Wolfram syndrome	D014929

LitCoin-GeneOrGeneProduct-v3

Id	Subject	Object	Predicate	Lexical cue
T1	26-30	GeneOrGeneProduct	denotes	WFS1

LitCoin_Mondo_095

Id	Subject	Object	Predicate	Lexical cue	mondo_id
T1	26-30	DiseaseOrPhenotypicFeature	denotes	WFS1	0009101
T2	82-98	DiseaseOrPhenotypicFeature	denotes	Wolfram syndrome	0018105

LitCoin-MeSH-Disease-2

Id	Subject	Object	Predicate	Lexical cue	ID:
T1	82-98	DiseaseOrPhenotypicFeature	denotes	Wolfram syndrome	D014929

LitCoin-MONDO_bioort2019

Id	Subject	Object	Predicate	Lexical cue	#label
T1	82-98	DiseaseOrPhenotypicFeature	denotes	Wolfram syndrome	D014929

LitCoin-Chemical-MeSH-CHEBI

Id	Subject	Object	Predicate	Lexical cue	ID:
T1	82-89	ChemicalEntity	denotes	Wolfram	D014414

LitCoin-NCBITaxon-2

Id	Subject	Object	Predicate	Lexical cue
T1	68-76	OrganismTaxon	denotes	patients

LitCoin-training-merged

Id	Subject	Object	Predicate	Lexical cue	#label	ID:
T1	82-89	ChemicalEntity	denotes	Wolfram		D014414
T10251	26-30	GeneOrGeneProduct	denotes	WFS1
T66029	82-98	DiseaseOrPhenotypicFeature	denotes	Wolfram syndrome	D014929
T27297	68-76	OrganismTaxon	denotes	patients

sentences

Id	Subject	Object	Predicate	Lexical cue
TextSentencer_T1	0-99	Sentence	denotes	Identification of a novel WFS1 mutation (AFF344-345ins) in Japanese patients with Wolfram syndrome.
T1	0-99	Sentence	denotes	Identification of a novel WFS1 mutation (AFF344-345ins) in Japanese patients with Wolfram syndrome.

DisGeNET5_gene_disease

Id	Subject	Object	Predicate	Lexical cue
16005363-0#26#30#gene7466	26-30	gene7466	denotes	WFS1
16005363-0#82#98#diseaseC0043207	82-98	diseaseC0043207	denotes	Wolfram syndrome
26#30#gene746682#98#diseaseC0043207	16005363-0#26#30#gene7466	16005363-0#82#98#diseaseC0043207	associated_with	WFS1,Wolfram syndrome

PubCasesORDO

Id	Subject	Object	Predicate	Lexical cue
TI1	82-98	ORDO:3463	denotes	Wolfram syndrome

tmVarCorpus

Id	Subject	Object	Predicate	Lexical cue
T1	41-54	ProteinMutation:p\|INS\|344_345\|AFF	denotes	AFF344-345ins

DisGeNET

Id	Subject	Object	Predicate	Lexical cue
T0	26-30	gene:7466	denotes	WFS1
T1	82-98	disease:C0043207	denotes	Wolfram syndrome
R1	T0	T1	associated_with	WFS1,Wolfram syndrome