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PubMed:23398170 / 181-366 JSON TXT

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sentences

Id	Subject	Object	Predicate	Lexical cue
TextSentencer_T2	0-185	Sentence	denotes	Incontinentia pigmenti (IP) is a rare X-linked dominant genodermatosis caused by mutations of the NEMO gene, which is required for activation of the nuclear factor-κB signaling pathway.
T2	0-185	Sentence	denotes	Incontinentia pigmenti (IP) is a rare X-linked dominant genodermatosis caused by mutations of the NEMO gene, which is required for activation of the nuclear factor-κB signaling pathway.

DisGeNET

Id	Subject	Object	Predicate	Lexical cue
T4	98-102	gene:8517	denotes	NEMO
T5	0-22	disease:C2930820	denotes	Incontinentia pigmenti
T6	98-102	gene:8517	denotes	NEMO
T7	0-22	disease:C0021171	denotes	Incontinentia pigmenti
R3	T4	T5	associated_with	NEMO,Incontinentia pigmenti
R4	T6	T7	associated_with	NEMO,Incontinentia pigmenti

Allie

Id	Subject	Object	Predicate	Lexical cue
SS1_23398170_1_0	0-22	expanded	denotes	Incontinentia pigmenti
SS2_23398170_1_0	24-26	abbr	denotes	IP
AE1_23398170_1_0	SS1_23398170_1_0	SS2_23398170_1_0	abbreviatedTo	Incontinentia pigmenti,IP

PubmedHPO

Id	Subject	Object	Predicate	Lexical cue
T1	38-55	HP_0001423	denotes	X-linked dominant
T2	38-46	HP_0001417	denotes	X-linked

PubCasesORDO

Id	Subject	Object	Predicate	Lexical cue
AB1	0-22	ORDO:464	denotes	Incontinentia pigmenti