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PubMed:12145188 / 102-228 JSONTXT

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sentences

Id Subject Object Predicate Lexical cue
TextSentencer_T2 0-126 Sentence denotes Recently, we reported a novel congenital disorder of glycosylation (CDG-IIb) caused by severe deficiency of the glucosidase I.
T2 0-126 Sentence denotes Recently, we reported a novel congenital disorder of glycosylation (CDG-IIb) caused by severe deficiency of the glucosidase I.

GlycoBiology-GDGDB

Id Subject Object Predicate Lexical cue
_T1 30-66 http://acgg.asia/db/diseases/gdgdb?con_ui=CON00360 denotes congenital disorder of glycosylation
_T2 30-66 http://acgg.asia/db/diseases/gdgdb?con_ui=CON00343 denotes congenital disorder of glycosylation
_T3 30-66 http://acgg.asia/db/diseases/gdgdb?con_ui=CON00344 denotes congenital disorder of glycosylation
_T4 30-66 http://acgg.asia/db/diseases/gdgdb?con_ui=CON00345 denotes congenital disorder of glycosylation
_T5 30-66 http://acgg.asia/db/diseases/gdgdb?con_ui=CON00346 denotes congenital disorder of glycosylation
_T6 30-66 http://acgg.asia/db/diseases/gdgdb?con_ui=CON00347 denotes congenital disorder of glycosylation
_T7 30-66 http://acgg.asia/db/diseases/gdgdb?con_ui=CON00348 denotes congenital disorder of glycosylation
_T8 30-66 http://acgg.asia/db/diseases/gdgdb?con_ui=CON00349 denotes congenital disorder of glycosylation
_T9 30-66 http://acgg.asia/db/diseases/gdgdb?con_ui=CON00350 denotes congenital disorder of glycosylation
_T10 30-66 http://acgg.asia/db/diseases/gdgdb?con_ui=CON00351 denotes congenital disorder of glycosylation
_T11 30-66 http://acgg.asia/db/diseases/gdgdb?con_ui=CON00352 denotes congenital disorder of glycosylation
_T12 30-66 http://acgg.asia/db/diseases/gdgdb?con_ui=CON00353 denotes congenital disorder of glycosylation
_T13 30-66 http://acgg.asia/db/diseases/gdgdb?con_ui=CON00354 denotes congenital disorder of glycosylation
_T14 30-66 http://acgg.asia/db/diseases/gdgdb?con_ui=CON00355 denotes congenital disorder of glycosylation
_T15 30-66 http://acgg.asia/db/diseases/gdgdb?con_ui=CON00356 denotes congenital disorder of glycosylation
_T16 30-66 http://acgg.asia/db/diseases/gdgdb?con_ui=CON00620 denotes congenital disorder of glycosylation
_T17 30-66 http://acgg.asia/db/diseases/gdgdb?con_ui=CON00627 denotes congenital disorder of glycosylation
_T18 30-66 http://acgg.asia/db/diseases/gdgdb?con_ui=CON00622 denotes congenital disorder of glycosylation
_T19 30-66 http://acgg.asia/db/diseases/gdgdb?con_ui=CON00623 denotes congenital disorder of glycosylation
_T20 30-66 http://acgg.asia/db/diseases/gdgdb?con_ui=CON00624 denotes congenital disorder of glycosylation
_T21 30-66 http://acgg.asia/db/diseases/gdgdb?con_ui=CON00625 denotes congenital disorder of glycosylation
_T22 30-66 http://acgg.asia/db/diseases/gdgdb?con_ui=CON00358 denotes congenital disorder of glycosylation
_T23 30-66 http://acgg.asia/db/diseases/gdgdb?con_ui=CON00359 denotes congenital disorder of glycosylation
_T24 30-66 http://acgg.asia/db/diseases/gdgdb?con_ui=CON00361 denotes congenital disorder of glycosylation
_T25 30-66 http://acgg.asia/db/diseases/gdgdb?con_ui=CON00362 denotes congenital disorder of glycosylation
_T26 30-66 http://acgg.asia/db/diseases/gdgdb?con_ui=CON00363 denotes congenital disorder of glycosylation
_T27 30-66 http://acgg.asia/db/diseases/gdgdb?con_ui=CON00364 denotes congenital disorder of glycosylation
_T28 30-66 http://acgg.asia/db/diseases/gdgdb?con_ui=CON00365 denotes congenital disorder of glycosylation
_T29 30-66 http://acgg.asia/db/diseases/gdgdb?con_ui=CON00367 denotes congenital disorder of glycosylation
_T30 30-66 http://acgg.asia/db/diseases/gdgdb?con_ui=CON00626 denotes congenital disorder of glycosylation
_T31 30-66 http://acgg.asia/db/diseases/gdgdb?con_ui=CON00621 denotes congenital disorder of glycosylation
_T32 68-75 http://acgg.asia/db/diseases/gdgdb?con_ui=CON00359 denotes CDG-IIb
_T33 68-75 http://acgg.asia/db/diseases/gdgdb?con_ui=CON00344 denotes CDG-IIb

GO-BP

Id Subject Object Predicate Lexical cue
T1 53-66 http://purl.obolibrary.org/obo/GO_0070085 denotes glycosylation

EDAM-DFO

Id Subject Object Predicate Lexical cue
T3 13-21 http://edamontology.org/data_2048 denotes reported

DisGeNET5_gene_disease

Id Subject Object Predicate Lexical cue
12145188-1#112#125#gene7841 112-125 gene7841 denotes glucosidase I
12145188-1#68#75#diseaseC1853736 68-75 diseaseC1853736 denotes CDG-IIb
112#125#gene784168#75#diseaseC1853736 12145188-1#112#125#gene7841 12145188-1#68#75#diseaseC1853736 associated_with glucosidase I,CDG-IIb

pubmed-enju-pas

Id Subject Object Predicate Lexical cue
EnjuParser_T17 0-8 RB denotes Recently
EnjuParser_T18 8-9 -COMMA- denotes ,
EnjuParser_T19 10-12 PRP denotes we
EnjuParser_T20 13-21 VBD denotes reported
EnjuParser_T21 22-23 DT denotes a
EnjuParser_T22 24-29 JJ denotes novel
EnjuParser_T23 30-40 JJ denotes congenital
EnjuParser_T24 41-49 NN denotes disorder
EnjuParser_T25 50-52 IN denotes of
EnjuParser_T26 53-66 NN denotes glycosylation
EnjuParser_T27 67-68 -LRB- denotes (
EnjuParser_T28 68-75 NN denotes CDG-IIb
EnjuParser_T29 75-76 -RRB- denotes )
EnjuParser_T30 77-83 VBN denotes caused
EnjuParser_T31 84-86 IN denotes by
EnjuParser_T32 87-93 JJ denotes severe
EnjuParser_T33 94-104 NN denotes deficiency
EnjuParser_T34 105-107 IN denotes of
EnjuParser_T35 108-111 DT denotes the
EnjuParser_T36 112-123 NN denotes glucosidase
EnjuParser_T37 124-126 NN denotes I.
EnjuParser_R16 EnjuParser_T20 EnjuParser_T17 arg1Of reported,Recently
EnjuParser_R17 EnjuParser_T20 EnjuParser_T18 arg1Of reported,","
EnjuParser_R18 EnjuParser_T19 EnjuParser_T20 arg1Of we,reported
EnjuParser_R20 EnjuParser_T24 EnjuParser_T21 arg1Of disorder,a
EnjuParser_R21 EnjuParser_T24 EnjuParser_T22 arg1Of disorder,novel
EnjuParser_R22 EnjuParser_T24 EnjuParser_T23 arg1Of disorder,congenital
EnjuParser_R23 EnjuParser_T24 EnjuParser_T25 arg1Of disorder,of
EnjuParser_R24 EnjuParser_T26 EnjuParser_T25 arg2Of glycosylation,of
EnjuParser_R25 EnjuParser_T26 EnjuParser_T27 arg1Of glycosylation,(
EnjuParser_R26 EnjuParser_T28 EnjuParser_T27 arg2Of CDG-IIb,(
EnjuParser_R27 EnjuParser_T29 EnjuParser_T27 arg3Of ),(
EnjuParser_R28 EnjuParser_T33 EnjuParser_T30 arg1Of deficiency,caused
EnjuParser_R29 EnjuParser_T24 EnjuParser_T30 arg2Of disorder,caused
EnjuParser_R30 EnjuParser_T33 EnjuParser_T31 arg2Of deficiency,by
EnjuParser_R31 EnjuParser_T33 EnjuParser_T32 arg1Of deficiency,severe
EnjuParser_R32 EnjuParser_T33 EnjuParser_T34 arg1Of deficiency,of
EnjuParser_R34 EnjuParser_T37 EnjuParser_T35 arg1Of I.,the
EnjuParser_R35 EnjuParser_T37 EnjuParser_T36 arg1Of I.,glucosidase

DisGeNET

Id Subject Object Predicate Lexical cue
T0 112-125 gene:7841 denotes glucosidase I
T1 30-49 disease:C0242354 denotes congenital disorder
T2 112-125 gene:7841 denotes glucosidase I
T3 68-75 disease:C1853736 denotes CDG-IIb
R1 T0 T1 associated_with glucosidase I,congenital disorder
R2 T2 T3 associated_with glucosidase I,CDG-IIb

mondo_disease

Id Subject Object Predicate Lexical cue mondo_id
T3 30-66 Disease denotes congenital disorder of glycosylation http://purl.obolibrary.org/obo/MONDO_0015286
T4 68-75 Disease denotes CDG-IIb http://purl.obolibrary.org/obo/MONDO_0011629