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PubMed:17549393 / 0-157 JSON TXT

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LitCoin-entities

Id	Subject	Object	Predicate	Lexical cue	db_id
4119	8-12	GeneOrGeneProduct	denotes	IRF6	NCBIGene:3664
4120	32-36	SequenceVariant	denotes	Y67X	p\|SUB\|Y\|67\|X
4121	62-84	DiseaseOrPhenotypicFeature	denotes	Van der Woude syndrome	MESH:C536528
4122	86-108	DiseaseOrPhenotypicFeature	denotes	Van der Woude syndrome	MESH:C536528
4123	110-113	DiseaseOrPhenotypicFeature	denotes	VWS	MESH:C536528

LitCoin-sentences

Id	Subject	Object	Predicate	Lexical cue
T1	0-85	Sentence	denotes	A novel IRF6 nonsense mutation (Y67X) in a German family with Van der Woude syndrome.

LitCoin_Mondo

Id	Subject	Object	Predicate	Lexical cue	mondo_id
T1	62-84	DiseaseOrPhenotypicFeature	denotes	Van der Woude syndrome	0019508
T2	86-108	DiseaseOrPhenotypicFeature	denotes	Van der Woude syndrome	0019508

LitCoin-SeqVar

Id	Subject	Object	Predicate	Lexical cue
T1	32-36	SequenceVariant	denotes	Y67X

LitCoin-GeneOrGeneProduct-v0

Id	Subject	Object	Predicate	Lexical cue
T1	2-7	GeneOrGeneProduct	denotes	novel
T2	8-12	GeneOrGeneProduct	denotes	IRF6
T3	22-30	GeneOrGeneProduct	denotes	mutation
T4	38-42	GeneOrGeneProduct	denotes	in a
T5	76-84	GeneOrGeneProduct	denotes	syndrome
T6	100-108	GeneOrGeneProduct	denotes	syndrome
T7	142-151	GeneOrGeneProduct	denotes	syndromic

LitCoin-GeneOrGeneProduct-v2

Id	Subject	Object	Predicate	Lexical cue
T1	2-7	GeneOrGeneProduct	denotes	novel
T2	8-12	GeneOrGeneProduct	denotes	IRF6
T3	76-84	GeneOrGeneProduct	denotes	syndrome
T4	100-108	GeneOrGeneProduct	denotes	syndrome

LitCoin-Disease-MeSH

Id	Subject	Object	Predicate	Lexical cue	originalLabel
T1	62-84	DiseaseOrPhenotypicFeature	denotes	Van der Woude syndrome	C536528
T2	86-108	DiseaseOrPhenotypicFeature	denotes	Van der Woude syndrome	C536528
T3	110-113	DiseaseOrPhenotypicFeature	denotes	VWS	C536528
T4	142-151	DiseaseOrPhenotypicFeature	denotes	syndromic	D013577

LitCoin-GeneOrGeneProduct-v3

Id	Subject	Object	Predicate	Lexical cue
T1	8-12	GeneOrGeneProduct	denotes	IRF6

LitCoin_Mondo_095

Id	Subject	Object	Predicate	Lexical cue	mondo_id
T1	62-84	DiseaseOrPhenotypicFeature	denotes	Van der Woude syndrome	0019508
T2	86-108	DiseaseOrPhenotypicFeature	denotes	Van der Woude syndrome	0019508
T3	110-113	DiseaseOrPhenotypicFeature	denotes	VWS	0019508

LitCoin-MeSH-Disease-2

Id	Subject	Object	Predicate	Lexical cue	ID:
T1	62-84	DiseaseOrPhenotypicFeature	denotes	Van der Woude syndrome	C536528
T2	86-108	DiseaseOrPhenotypicFeature	denotes	Van der Woude syndrome	C536528
T3	110-113	DiseaseOrPhenotypicFeature	denotes	VWS	C536528

LitCoin-MONDO_bioort2019

Id	Subject	Object	Predicate	Lexical cue	#label
T1	62-84	DiseaseOrPhenotypicFeature	denotes	Van der Woude syndrome	C536528
T2	86-108	DiseaseOrPhenotypicFeature	denotes	Van der Woude syndrome	C536528
T3	110-113	DiseaseOrPhenotypicFeature	denotes	VWS	C536528

LitCoin-training-merged

Id	Subject	Object	Predicate	Lexical cue	#label
T92598	8-12	GeneOrGeneProduct	denotes	IRF6
T73165	110-113	DiseaseOrPhenotypicFeature	denotes	VWS	C536528
T29454	86-108	DiseaseOrPhenotypicFeature	denotes	Van der Woude syndrome	C536528
T89410	62-84	DiseaseOrPhenotypicFeature	denotes	Van der Woude syndrome	C536528
T61975	32-36	SequenceVariant	denotes	Y67X

DisGeNET

Id	Subject	Object	Predicate	Lexical cue
T0	8-12	gene:3664	denotes	IRF6
T1	62-84	disease:C0175697	denotes	Van der Woude syndrome
R1	T0	T1	associated_with	IRF6,Van der Woude syndrome

DisGeNET5_gene_disease

Id	Subject	Object	Predicate	Lexical cue
17549393-0#8#12#gene3664	8-12	gene3664	denotes	IRF6
17549393-0#62#84#diseaseC0175697	62-84	diseaseC0175697	denotes	Van der Woude syndrome
8#12#gene366462#84#diseaseC0175697	17549393-0#8#12#gene3664	17549393-0#62#84#diseaseC0175697	associated_with	IRF6,Van der Woude syndrome

tmVarCorpus

Id	Subject	Object	Predicate	Lexical cue
T1	32-36	ProteinMutation:p\|SUB\|Y\|67\|X	denotes	Y67X