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PubMed:22016685 JSON TXT

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DisGeNET

Id	Subject	Object	Predicate	Lexical cue
T0	54-57	gene:2160	denotes	F11
T1	105-125	disease:C0015523	denotes	factor XI deficiency
R1	T0	T1	associated_with	F11,factor XI deficiency

PubmedHPO

Id	Subject	Object	Predicate	Lexical cue
T1	164-183	HP_0000007	denotes	autosomal recessive
T2	184-204	HP_0001928	denotes	coagulation disorder
T3	776-782	HP_0012032	denotes	lipoma
T4	813-860	HP_0003645	denotes	prolonged activated partial thromboplastin time

Allie

Id	Subject	Object	Predicate	Lexical cue
SS1_22016685_1_0	127-136	expanded	denotes	Factor XI
SS2_22016685_1_0	138-141	abbr	denotes	FXI
AE1_22016685_1_0	SS1_22016685_1_0	SS2_22016685_1_0	abbreviatedTo	Factor XI,FXI

DisGeNET5_variant_disease

Id	Subject	Object	Predicate	Lexical cue
22016685-0#26#35#geners281875258	26-35	geners281875258	denotes	Asp506Gly
22016685-0#105#125#diseaseC0015523	105-125	diseaseC0015523	denotes	factor XI deficiency
26#35#geners281875258105#125#diseaseC0015523	22016685-0#26#35#geners281875258	22016685-0#105#125#diseaseC0015523	associated_with	Asp506Gly,factor XI deficiency

DisGeNET5_gene_disease

Id	Subject	Object	Predicate	Lexical cue
22016685-0#54#57#gene2160	54-57	gene2160	denotes	F11
22016685-0#105#125#diseaseC0015523	105-125	diseaseC0015523	denotes	factor XI deficiency
54#57#gene2160105#125#diseaseC0015523	22016685-0#54#57#gene2160	22016685-0#105#125#diseaseC0015523	associated_with	F11,factor XI deficiency

PubCasesHPO

Id	Subject	Object	Predicate	Lexical cue
AB1	776-782	HP:0012032	denotes	lipoma

tmVarCorpus

Id	Subject	Object	Predicate	Lexical cue
T1	26-35	ProteinMutation:p\|SUB\|D\|506\|G	denotes	Asp506Gly
T2	1109-1118	DNAMutation:c\|SUB\|A\|1517\|G	denotes	c.1517A>G
T3	1206-1217	ProteinMutation:p\|SUB\|D\|506\|G	denotes	p.Asp506Gly
T4	1254-1263	ProteinMutation:p\|SUB\|D\|506\|G	denotes	Asp506Gly