> top > docs > PubMed:16321363 > spans > 0-89 > annotations

PubMed:16321363 / 0-89 JSON TXT

Annnotations TAB JSON ListView MergeView

TEST-DiseaseOrPhenotypicFeature

Id	Subject	Object	Predicate	Lexical cue	#label
T1	0-36	DiseaseOrPhenotypicFeature	denotes	Congenital disorder of glycosylation	D018981

Test-merged

Id	Subject	Object	Predicate	Lexical cue	#label
T1	0-36	DiseaseOrPhenotypicFeature	denotes	Congenital disorder of glycosylation	D018981

Test-merged-2

Id	Subject	Object	Predicate	Lexical cue	#label
T1	0-36	DiseaseOrPhenotypicFeature	denotes	Congenital disorder of glycosylation	D018981

sentences

Id	Subject	Object	Predicate	Lexical cue
TextSentencer_T1	0-89	Sentence	denotes	Congenital disorder of glycosylation Ic due to a de novo deletion and an hALG-6 mutation.
T1	0-89	Sentence	denotes	Congenital disorder of glycosylation Ic due to a de novo deletion and an hALG-6 mutation.