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PubMed:15917429 / 125-403 JSONTXT

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CL-cell

Id Subject Object Predicate Lexical cue cl_id
T3 0-9 Cell denotes Leukocyte http://purl.obolibrary.org/obo/CL:0000738
T4 192-201 Cell denotes leukocyte http://purl.obolibrary.org/obo/CL:0000738

Glycan-Motif

Id Subject Object Predicate Lexical cue
T1 152-158 https://glytoucan.org/Structures/Glycans/G82576YO denotes fucose

GlyCosmos6-Glycan-Motif-Image

Id Subject Object Predicate Lexical cue image
T1 152-158 Glycan_Motif denotes fucose https://api.glycosmos.org/wurcs2image/0.10.0/png/binary/G82576YO

GlyCosmos6-Glycan-Motif-Structure

Id Subject Object Predicate Lexical cue
T1 152-158 https://glytoucan.org/Structures/Glycans/G82576YO denotes fucose

GlycoBiology-GDGDB

Id Subject Object Predicate Lexical cue
_T33 0-29 http://acgg.asia/db/diseases/gdgdb?con_ui=CON00360 denotes Leukocyte adhesion deficiency
_T34 30-66 http://acgg.asia/db/diseases/gdgdb?con_ui=CON00349 denotes congenital disorder of glycosylation
_T35 30-66 http://acgg.asia/db/diseases/gdgdb?con_ui=CON00355 denotes congenital disorder of glycosylation
_T36 30-66 http://acgg.asia/db/diseases/gdgdb?con_ui=CON00622 denotes congenital disorder of glycosylation
_T37 30-66 http://acgg.asia/db/diseases/gdgdb?con_ui=CON00354 denotes congenital disorder of glycosylation
_T38 30-66 http://acgg.asia/db/diseases/gdgdb?con_ui=CON00623 denotes congenital disorder of glycosylation
_T39 30-66 http://acgg.asia/db/diseases/gdgdb?con_ui=CON00353 denotes congenital disorder of glycosylation
_T40 30-66 http://acgg.asia/db/diseases/gdgdb?con_ui=CON00624 denotes congenital disorder of glycosylation
_T41 30-66 http://acgg.asia/db/diseases/gdgdb?con_ui=CON00352 denotes congenital disorder of glycosylation
_T42 30-66 http://acgg.asia/db/diseases/gdgdb?con_ui=CON00625 denotes congenital disorder of glycosylation
_T43 30-66 http://acgg.asia/db/diseases/gdgdb?con_ui=CON00351 denotes congenital disorder of glycosylation
_T44 30-66 http://acgg.asia/db/diseases/gdgdb?con_ui=CON00358 denotes congenital disorder of glycosylation
_T45 30-66 http://acgg.asia/db/diseases/gdgdb?con_ui=CON00350 denotes congenital disorder of glycosylation
_T46 30-66 http://acgg.asia/db/diseases/gdgdb?con_ui=CON00359 denotes congenital disorder of glycosylation
_T47 30-66 http://acgg.asia/db/diseases/gdgdb?con_ui=CON00360 denotes congenital disorder of glycosylation
_T48 30-66 http://acgg.asia/db/diseases/gdgdb?con_ui=CON00361 denotes congenital disorder of glycosylation
_T49 30-66 http://acgg.asia/db/diseases/gdgdb?con_ui=CON00621 denotes congenital disorder of glycosylation
_T50 30-66 http://acgg.asia/db/diseases/gdgdb?con_ui=CON00343 denotes congenital disorder of glycosylation
_T51 30-66 http://acgg.asia/db/diseases/gdgdb?con_ui=CON00348 denotes congenital disorder of glycosylation
_T52 30-66 http://acgg.asia/db/diseases/gdgdb?con_ui=CON00363 denotes congenital disorder of glycosylation
_T53 30-66 http://acgg.asia/db/diseases/gdgdb?con_ui=CON00347 denotes congenital disorder of glycosylation
_T54 30-66 http://acgg.asia/db/diseases/gdgdb?con_ui=CON00364 denotes congenital disorder of glycosylation
_T55 30-66 http://acgg.asia/db/diseases/gdgdb?con_ui=CON00346 denotes congenital disorder of glycosylation
_T56 30-66 http://acgg.asia/db/diseases/gdgdb?con_ui=CON00365 denotes congenital disorder of glycosylation
_T57 30-66 http://acgg.asia/db/diseases/gdgdb?con_ui=CON00620 denotes congenital disorder of glycosylation
_T58 30-66 http://acgg.asia/db/diseases/gdgdb?con_ui=CON00367 denotes congenital disorder of glycosylation
_T59 30-66 http://acgg.asia/db/diseases/gdgdb?con_ui=CON00356 denotes congenital disorder of glycosylation
_T60 30-66 http://acgg.asia/db/diseases/gdgdb?con_ui=CON00626 denotes congenital disorder of glycosylation
_T61 30-66 http://acgg.asia/db/diseases/gdgdb?con_ui=CON00344 denotes congenital disorder of glycosylation
_T62 30-66 http://acgg.asia/db/diseases/gdgdb?con_ui=CON00627 denotes congenital disorder of glycosylation
_T63 30-66 http://acgg.asia/db/diseases/gdgdb?con_ui=CON00362 denotes congenital disorder of glycosylation
_T64 30-70 http://acgg.asia/db/diseases/gdgdb?con_ui=CON00345 denotes congenital disorder of glycosylation IIc
_T65 79-86 http://acgg.asia/db/diseases/gdgdb?con_ui=CON00345 denotes CDG IIc
_T66 79-86 http://acgg.asia/db/diseases/gdgdb?con_ui=CON00360 denotes CDG IIc
_T67 79-90 http://acgg.asia/db/diseases/gdgdb?con_ui=CON00624 denotes CDG IIc) is
_T68 192-221 http://acgg.asia/db/diseases/gdgdb?con_ui=CON00360 denotes leukocyte adhesion deficiency

uniprot-human

Id Subject Object Predicate Lexical cue
T1 72-75 http://www.uniprot.org/uniprot/P09622 denotes LAD
T6 72-75 http://www.uniprot.org/uniprot/O00515 denotes LAD

GO-BP

Id Subject Object Predicate Lexical cue
T10 0-18 http://purl.obolibrary.org/obo/GO_0007159 denotes Leukocyte adhesion
T12 53-66 http://purl.obolibrary.org/obo/GO_0070085 denotes glycosylation

sentences

Id Subject Object Predicate Lexical cue
TextSentencer_T2 0-278 Sentence denotes Leukocyte adhesion deficiency/congenital disorder of glycosylation IIc (LAD II/CDG IIc) is a genetic disease characterized by a decreased expression of fucose in glycoconjugates, resulting in leukocyte adhesion deficiency and severe morphological and neurological abnormalities.
T2 0-278 Sentence denotes Leukocyte adhesion deficiency/congenital disorder of glycosylation IIc (LAD II/CDG IIc) is a genetic disease characterized by a decreased expression of fucose in glycoconjugates, resulting in leukocyte adhesion deficiency and severe morphological and neurological abnormalities.
T2 0-278 Sentence denotes Leukocyte adhesion deficiency/congenital disorder of glycosylation IIc (LAD II/CDG IIc) is a genetic disease characterized by a decreased expression of fucose in glycoconjugates, resulting in leukocyte adhesion deficiency and severe morphological and neurological abnormalities.

mondo_disease

Id Subject Object Predicate Lexical cue mondo_id
T3 0-29 Disease denotes Leukocyte adhesion deficiency http://purl.obolibrary.org/obo/MONDO_0017570
T4 30-66 Disease denotes congenital disorder of glycosylation http://purl.obolibrary.org/obo/MONDO_0015286
T5 72-75 Disease denotes LAD http://purl.obolibrary.org/obo/MONDO_0017570
T6 79-86 Disease denotes CDG IIc http://purl.obolibrary.org/obo/MONDO_0009953
T7 93-108 Disease denotes genetic disease http://purl.obolibrary.org/obo/MONDO_0003847
T8 192-221 Disease denotes leukocyte adhesion deficiency http://purl.obolibrary.org/obo/MONDO_0017570

HP-phenotype

Id Subject Object Predicate Lexical cue hp_id
T1 251-277 Phenotype denotes neurological abnormalities HP:0000707

Anatomy-UBERON

Id Subject Object Predicate Lexical cue uberon_id
T3 0-9 Body_part denotes Leukocyte http://purl.obolibrary.org/obo/CL_0000738
T4 192-201 Body_part denotes leukocyte http://purl.obolibrary.org/obo/CL_0000738