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PubMed:16037488 / 118-378 JSONTXT

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Glycan-Motif

Id Subject Object Predicate Lexical cue
T1 32-41 https://glytoucan.org/Structures/Glycans/G65889KE denotes galactose
T2 32-41 https://glytoucan.org/Structures/Glycans/G68158BT denotes galactose
T3 176-185 https://glytoucan.org/Structures/Glycans/G65889KE denotes galactose
T4 176-185 https://glytoucan.org/Structures/Glycans/G68158BT denotes galactose

GlyCosmos6-Glycan-Motif-Image

Id Subject Object Predicate Lexical cue image
T1 32-41 Glycan_Motif denotes galactose https://api.glycosmos.org/wurcs2image/0.10.0/png/binary/G68158BT|https://api.glycosmos.org/wurcs2image/0.10.0/png/binary/G65889KE
T3 176-185 Glycan_Motif denotes galactose https://api.glycosmos.org/wurcs2image/0.10.0/png/binary/G68158BT|https://api.glycosmos.org/wurcs2image/0.10.0/png/binary/G65889KE

GlyCosmos6-Glycan-Motif-Structure

Id Subject Object Predicate Lexical cue
T1 32-41 https://glytoucan.org/Structures/Glycans/G65889KE denotes galactose
T2 32-41 https://glytoucan.org/Structures/Glycans/G68158BT denotes galactose
T3 176-185 https://glytoucan.org/Structures/Glycans/G65889KE denotes galactose
T4 176-185 https://glytoucan.org/Structures/Glycans/G68158BT denotes galactose

GlycoBiology-GDGDB

Id Subject Object Predicate Lexical cue
_T1 115-152 http://acgg.asia/db/diseases/gdgdb?con_ui=CON00360 denotes congenital disorders of glycosylation
_T2 115-152 http://acgg.asia/db/diseases/gdgdb?con_ui=CON00343 denotes congenital disorders of glycosylation
_T3 115-152 http://acgg.asia/db/diseases/gdgdb?con_ui=CON00344 denotes congenital disorders of glycosylation
_T4 115-152 http://acgg.asia/db/diseases/gdgdb?con_ui=CON00345 denotes congenital disorders of glycosylation
_T5 115-152 http://acgg.asia/db/diseases/gdgdb?con_ui=CON00346 denotes congenital disorders of glycosylation
_T6 115-152 http://acgg.asia/db/diseases/gdgdb?con_ui=CON00347 denotes congenital disorders of glycosylation
_T7 115-152 http://acgg.asia/db/diseases/gdgdb?con_ui=CON00348 denotes congenital disorders of glycosylation
_T8 115-152 http://acgg.asia/db/diseases/gdgdb?con_ui=CON00349 denotes congenital disorders of glycosylation
_T9 115-152 http://acgg.asia/db/diseases/gdgdb?con_ui=CON00350 denotes congenital disorders of glycosylation
_T10 115-152 http://acgg.asia/db/diseases/gdgdb?con_ui=CON00351 denotes congenital disorders of glycosylation
_T11 115-152 http://acgg.asia/db/diseases/gdgdb?con_ui=CON00352 denotes congenital disorders of glycosylation
_T12 115-152 http://acgg.asia/db/diseases/gdgdb?con_ui=CON00353 denotes congenital disorders of glycosylation
_T13 115-152 http://acgg.asia/db/diseases/gdgdb?con_ui=CON00354 denotes congenital disorders of glycosylation
_T14 115-152 http://acgg.asia/db/diseases/gdgdb?con_ui=CON00355 denotes congenital disorders of glycosylation
_T15 115-152 http://acgg.asia/db/diseases/gdgdb?con_ui=CON00356 denotes congenital disorders of glycosylation
_T16 115-152 http://acgg.asia/db/diseases/gdgdb?con_ui=CON00620 denotes congenital disorders of glycosylation
_T17 115-152 http://acgg.asia/db/diseases/gdgdb?con_ui=CON00627 denotes congenital disorders of glycosylation
_T18 115-152 http://acgg.asia/db/diseases/gdgdb?con_ui=CON00622 denotes congenital disorders of glycosylation
_T19 115-152 http://acgg.asia/db/diseases/gdgdb?con_ui=CON00623 denotes congenital disorders of glycosylation
_T20 115-152 http://acgg.asia/db/diseases/gdgdb?con_ui=CON00624 denotes congenital disorders of glycosylation
_T21 115-152 http://acgg.asia/db/diseases/gdgdb?con_ui=CON00625 denotes congenital disorders of glycosylation
_T22 115-152 http://acgg.asia/db/diseases/gdgdb?con_ui=CON00358 denotes congenital disorders of glycosylation
_T23 115-152 http://acgg.asia/db/diseases/gdgdb?con_ui=CON00359 denotes congenital disorders of glycosylation
_T24 115-152 http://acgg.asia/db/diseases/gdgdb?con_ui=CON00361 denotes congenital disorders of glycosylation
_T25 115-152 http://acgg.asia/db/diseases/gdgdb?con_ui=CON00362 denotes congenital disorders of glycosylation
_T26 115-152 http://acgg.asia/db/diseases/gdgdb?con_ui=CON00363 denotes congenital disorders of glycosylation
_T27 115-152 http://acgg.asia/db/diseases/gdgdb?con_ui=CON00364 denotes congenital disorders of glycosylation
_T28 115-152 http://acgg.asia/db/diseases/gdgdb?con_ui=CON00365 denotes congenital disorders of glycosylation
_T29 115-152 http://acgg.asia/db/diseases/gdgdb?con_ui=CON00367 denotes congenital disorders of glycosylation
_T30 115-152 http://acgg.asia/db/diseases/gdgdb?con_ui=CON00626 denotes congenital disorders of glycosylation
_T31 115-152 http://acgg.asia/db/diseases/gdgdb?con_ui=CON00621 denotes congenital disorders of glycosylation
_T32 252-258 http://acgg.asia/db/diseases/gdgdb?con_ui=CON00351 denotes CDG-II

uniprot-human

Id Subject Object Predicate Lexical cue
T4 73-77 http://www.uniprot.org/uniprot/Q53XK1 denotes GALT

GO-BP

Id Subject Object Predicate Lexical cue
T3 139-152 http://purl.obolibrary.org/obo/GO_0070085 denotes glycosylation

DisGeNET5_gene_disease

Id Subject Object Predicate Lexical cue
16037488-1#252#258#gene7045 252-258 gene7045 denotes CDG-II
16037488-1#10#30#diseaseC0268151 10-30 diseaseC0268151 denotes classic galactosemia
16037488-1#73#89#diseaseC0268151 73-89 diseaseC0268151 denotes GALT] deficiency
16037488-1#115#152#diseaseC0282577 115-152 diseaseC0282577 denotes congenital disorders of glycosylation
16037488-1#154#157#diseaseC0282577 154-157 diseaseC0282577 denotes CDG
252#258#gene704510#30#diseaseC0268151 16037488-1#252#258#gene7045 16037488-1#10#30#diseaseC0268151 associated_with CDG-II,classic galactosemia
252#258#gene704573#89#diseaseC0268151 16037488-1#252#258#gene7045 16037488-1#73#89#diseaseC0268151 associated_with CDG-II,GALT] deficiency
252#258#gene7045115#152#diseaseC0282577 16037488-1#252#258#gene7045 16037488-1#115#152#diseaseC0282577 associated_with CDG-II,congenital disorders of glycosylation
252#258#gene7045154#157#diseaseC0282577 16037488-1#252#258#gene7045 16037488-1#154#157#diseaseC0282577 associated_with CDG-II,CDG

sentences

Id Subject Object Predicate Lexical cue
TextSentencer_T2 0-260 Sentence denotes Untreated classic galactosemia (galactose-1-phosphate uridyltransferase [GALT] deficiency) is known as a secondary congenital disorders of glycosylation (CDG) characterized by galactose deficiency of glycoproteins and glycolipids (processing defect or CDG-II).
T2 0-260 Sentence denotes Untreated classic galactosemia (galactose-1-phosphate uridyltransferase [GALT] deficiency) is known as a secondary congenital disorders of glycosylation (CDG) characterized by galactose deficiency of glycoproteins and glycolipids (processing defect or CDG-II).
T2 0-260 Sentence denotes Untreated classic galactosemia (galactose-1-phosphate uridyltransferase [GALT] deficiency) is known as a secondary congenital disorders of glycosylation (CDG) characterized by galactose deficiency of glycoproteins and glycolipids (processing defect or CDG-II).

DisGeNET

Id Subject Object Predicate Lexical cue
T0 252-258 gene:7045 denotes CDG-II
T1 10-30 disease:C0268151 denotes classic galactosemia
T2 252-258 gene:7045 denotes CDG-II
T3 73-89 disease:C0268151 denotes GALT] deficiency
T4 252-258 gene:7045 denotes CDG-II
T5 115-152 disease:C0282577 denotes congenital disorders of glycosylation
T6 252-258 gene:7045 denotes CDG-II
T7 154-157 disease:C0282577 denotes CDG
R1 T0 T1 associated_with CDG-II,classic galactosemia
R2 T2 T3 associated_with CDG-II,GALT] deficiency
R3 T4 T5 associated_with CDG-II,congenital disorders of glycosylation
R4 T6 T7 associated_with CDG-II,CDG

HP-phenotype

Id Subject Object Predicate Lexical cue hp_id
T2 18-30 Phenotype denotes galactosemia HP:0012024

mondo_disease

Id Subject Object Predicate Lexical cue mondo_id
T3 10-30 Disease denotes classic galactosemia http://purl.obolibrary.org/obo/MONDO_0009258
T4 73-89 Disease denotes GALT] deficiency http://purl.obolibrary.org/obo/MONDO_0009258
T5 115-152 Disease denotes congenital disorders of glycosylation http://purl.obolibrary.org/obo/MONDO_0015286
T6 154-157 Disease denotes CDG http://purl.obolibrary.org/obo/MONDO_0015286
T7 252-258 Disease denotes CDG-II http://purl.obolibrary.org/obo/MONDO_0011933
T8 252-255 Disease denotes CDG http://purl.obolibrary.org/obo/MONDO_0015286

Anatomy-UBERON

Id Subject Object Predicate Lexical cue uberon_id
T1 73-77 Body_part denotes GALT http://purl.obolibrary.org/obo/UBERON_0001962