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PubMed:12626422 / 0-112 JSONTXT

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GlycoBiology-GDGDB

Id Subject Object Predicate Lexical cue
_T1 56-98 http://acgg.asia/db/diseases/gdgdb?con_ui=CON00347 denotes congenital disorders of glycosylation type
_T2 56-98 http://acgg.asia/db/diseases/gdgdb?con_ui=CON00362 denotes congenital disorders of glycosylation type
_T3 56-100 http://acgg.asia/db/diseases/gdgdb?con_ui=CON00349 denotes congenital disorders of glycosylation type I
_T4 56-100 http://acgg.asia/db/diseases/gdgdb?con_ui=CON00343 denotes congenital disorders of glycosylation type I
_T5 56-100 http://acgg.asia/db/diseases/gdgdb?con_ui=CON00367 denotes congenital disorders of glycosylation type I
_T6 56-100 http://acgg.asia/db/diseases/gdgdb?con_ui=CON00344 denotes congenital disorders of glycosylation type I
_T7 56-100 http://acgg.asia/db/diseases/gdgdb?con_ui=CON00365 denotes congenital disorders of glycosylation type I
_T8 56-100 http://acgg.asia/db/diseases/gdgdb?con_ui=CON00345 denotes congenital disorders of glycosylation type I
_T9 56-100 http://acgg.asia/db/diseases/gdgdb?con_ui=CON00364 denotes congenital disorders of glycosylation type I
_T10 56-100 http://acgg.asia/db/diseases/gdgdb?con_ui=CON00346 denotes congenital disorders of glycosylation type I
_T11 56-100 http://acgg.asia/db/diseases/gdgdb?con_ui=CON00363 denotes congenital disorders of glycosylation type I
_T12 56-100 http://acgg.asia/db/diseases/gdgdb?con_ui=CON00627 denotes congenital disorders of glycosylation type I
_T13 56-100 http://acgg.asia/db/diseases/gdgdb?con_ui=CON00360 denotes congenital disorders of glycosylation type I
_T14 56-100 http://acgg.asia/db/diseases/gdgdb?con_ui=CON00348 denotes congenital disorders of glycosylation type I
_T15 56-100 http://acgg.asia/db/diseases/gdgdb?con_ui=CON00361 denotes congenital disorders of glycosylation type I
_T16 56-100 http://acgg.asia/db/diseases/gdgdb?con_ui=CON00626 denotes congenital disorders of glycosylation type I
_T17 56-100 http://acgg.asia/db/diseases/gdgdb?con_ui=CON00359 denotes congenital disorders of glycosylation type I
_T18 56-100 http://acgg.asia/db/diseases/gdgdb?con_ui=CON00350 denotes congenital disorders of glycosylation type I
_T19 56-100 http://acgg.asia/db/diseases/gdgdb?con_ui=CON00358 denotes congenital disorders of glycosylation type I
_T20 56-100 http://acgg.asia/db/diseases/gdgdb?con_ui=CON00351 denotes congenital disorders of glycosylation type I
_T21 56-100 http://acgg.asia/db/diseases/gdgdb?con_ui=CON00625 denotes congenital disorders of glycosylation type I
_T22 56-100 http://acgg.asia/db/diseases/gdgdb?con_ui=CON00352 denotes congenital disorders of glycosylation type I
_T23 56-100 http://acgg.asia/db/diseases/gdgdb?con_ui=CON00624 denotes congenital disorders of glycosylation type I
_T24 56-100 http://acgg.asia/db/diseases/gdgdb?con_ui=CON00353 denotes congenital disorders of glycosylation type I
_T25 56-100 http://acgg.asia/db/diseases/gdgdb?con_ui=CON00623 denotes congenital disorders of glycosylation type I
_T26 56-100 http://acgg.asia/db/diseases/gdgdb?con_ui=CON00354 denotes congenital disorders of glycosylation type I
_T27 56-100 http://acgg.asia/db/diseases/gdgdb?con_ui=CON00622 denotes congenital disorders of glycosylation type I
_T28 56-100 http://acgg.asia/db/diseases/gdgdb?con_ui=CON00355 denotes congenital disorders of glycosylation type I
_T29 56-100 http://acgg.asia/db/diseases/gdgdb?con_ui=CON00621 denotes congenital disorders of glycosylation type I
_T30 56-100 http://acgg.asia/db/diseases/gdgdb?con_ui=CON00356 denotes congenital disorders of glycosylation type I
_T31 56-100 http://acgg.asia/db/diseases/gdgdb?con_ui=CON00620 denotes congenital disorders of glycosylation type I

GlycoBiology-FMA

Id Subject Object Predicate Lexical cue
_T1 26-32 FMAID:162307 denotes plasma

uniprot-human

Id Subject Object Predicate Lexical cue
T1 33-52 http://www.uniprot.org/uniprot/Q86U18 denotes alpha 1-antitrypsin

GO-BP

Id Subject Object Predicate Lexical cue
T1 80-93 http://purl.obolibrary.org/obo/GO_0070085 denotes glycosylation

DisGeNET5_gene_disease

Id Subject Object Predicate Lexical cue
12626422-0#33#52#gene5265 33-52 gene5265 denotes alpha 1-antitrypsin
12626422-0#56#93#diseaseC0282577 56-93 diseaseC0282577 denotes congenital disorders of glycosylation
33#52#gene526556#93#diseaseC0282577 12626422-0#33#52#gene5265 12626422-0#56#93#diseaseC0282577 associated_with alpha 1-antitrypsin,congenital disorders of glycosylation

DisGeNET

Id Subject Object Predicate Lexical cue
T0 33-52 gene:5265 denotes alpha 1-antitrypsin
T1 56-93 disease:C0282577 denotes congenital disorders of glycosylation
R1 T0 T1 associated_with alpha 1-antitrypsin,congenital disorders of glycosylation

mondo_disease

Id Subject Object Predicate Lexical cue mondo_id
T1 56-100 Disease denotes congenital disorders of glycosylation type I http://purl.obolibrary.org/obo/MONDO_0005500

Anatomy-UBERON

Id Subject Object Predicate Lexical cue uberon_id
T1 26-32 Body_part denotes plasma http://purl.obolibrary.org/obo/UBERON_0001969

CL-cell

Id Subject Object Predicate Lexical cue cl_id
T1 94-100 Cell denotes type I http://purl.obolibrary.org/obo/CL:0004120|http://purl.obolibrary.org/obo/CL:0004138