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PubMed:19757027 JSONTXT

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CL-cell

Id Subject Object Predicate Lexical cue cl_id
T1 139-150 Cell denotes erythrocyte http://purl.obolibrary.org/obo/CL:0000232
T2 519-531 Cell denotes erythrocytes http://purl.obolibrary.org/obo/CL:0000232
T3 888-900 Cell denotes erythrocytes http://purl.obolibrary.org/obo/CL:0000232

GlyCosmos6-Glycan-Motif-Image

Id Subject Object Predicate Lexical cue image
T1 633-644 Glycan_Motif denotes sialic acid https://api.glycosmos.org/wurcs2image/0.10.0/png/binary/G81533KY

GlyCosmos6-Glycan-Motif-Structure

Id Subject Object Predicate Lexical cue
T1 633-644 https://glytoucan.org/Structures/Glycans/G81533KY denotes sialic acid

sentences

Id Subject Object Predicate Lexical cue
TextSentencer_T1 0-79 Sentence denotes Eryptosis in hereditary spherocytosis and thalassemia: role of glycoconjugates.
TextSentencer_T2 80-342 Sentence denotes The present work is aimed to study the mechanism of faster erythrocyte clearance in hereditary spherocytosis (HS), a heterogeneous disorders characterized by alterations in the proteins of the red cell membrane skeleton along with different kinds of thalassemia.
TextSentencer_T3 343-453 Sentence denotes The maximum exposure of phosphatidylserine (PS) is found in HS compared to those in both α- and β-thalassemia.
TextSentencer_T4 454-624 Sentence denotes Interestingly, in HS more PS exposed cells were found in younger erythrocytes compared to normal and the thalassemics where aged cells showed higher loss of PS asymmetry.
TextSentencer_T5 625-736 Sentence denotes Loss of sialic acid and GlcNAc bearing glycoconjugates, presumably the glycophorins, was also found upon aging.
TextSentencer_T6 737-968 Sentence denotes The loss of PS asymmetry together with the cell surface glycoproteins mediated by membrane vesiculation, seemed to play key role in early clearance of erythrocytes from circulation following a mechanism similar to HbEβ-thalassemia.
T1 0-79 Sentence denotes Eryptosis in hereditary spherocytosis and thalassemia: role of glycoconjugates.
T2 80-342 Sentence denotes The present work is aimed to study the mechanism of faster erythrocyte clearance in hereditary spherocytosis (HS), a heterogeneous disorders characterized by alterations in the proteins of the red cell membrane skeleton along with different kinds of thalassemia.
T3 343-453 Sentence denotes The maximum exposure of phosphatidylserine (PS) is found in HS compared to those in both α- and β-thalassemia.
T4 454-624 Sentence denotes Interestingly, in HS more PS exposed cells were found in younger erythrocytes compared to normal and the thalassemics where aged cells showed higher loss of PS asymmetry.
T5 625-736 Sentence denotes Loss of sialic acid and GlcNAc bearing glycoconjugates, presumably the glycophorins, was also found upon aging.
T6 737-968 Sentence denotes The loss of PS asymmetry together with the cell surface glycoproteins mediated by membrane vesiculation, seemed to play key role in early clearance of erythrocytes from circulation following a mechanism similar to HbEβ-thalassemia.

Glycosmos6-MAT

Id Subject Object Predicate Lexical cue
T1 291-299 http://purl.obolibrary.org/obo/MAT_0000032 denotes skeleton

Allie

Id Subject Object Predicate Lexical cue
SS1_19757027_1_0 164-188 expanded denotes hereditary spherocytosis
SS2_19757027_1_0 190-192 abbr denotes HS
SS1_19757027_2_0 367-385 expanded denotes phosphatidylserine
SS2_19757027_2_0 387-389 abbr denotes PS
AE1_19757027_1_0 SS1_19757027_1_0 SS2_19757027_1_0 abbreviatedTo hereditary spherocytosis,HS
AE1_19757027_2_0 SS1_19757027_2_0 SS2_19757027_2_0 abbreviatedTo phosphatidylserine,PS

NGLY1-deficiency

Id Subject Object Predicate Lexical cue
PD-NGLY1-deficiency-B_T1 649-655 chem:24139 denotes GlcNAc

mondo_disease

Id Subject Object Predicate Lexical cue mondo_id
T1 13-37 Disease denotes hereditary spherocytosis http://purl.obolibrary.org/obo/MONDO_0019350
T2 42-53 Disease denotes thalassemia http://purl.obolibrary.org/obo/MONDO_0000984
T3 164-188 Disease denotes hereditary spherocytosis http://purl.obolibrary.org/obo/MONDO_0019350
T4 190-192 Disease denotes HS http://purl.obolibrary.org/obo/MONDO_0019350
T5 330-341 Disease denotes thalassemia http://purl.obolibrary.org/obo/MONDO_0000984
T6 403-405 Disease denotes HS http://purl.obolibrary.org/obo/MONDO_0019350
T7 441-452 Disease denotes thalassemia http://purl.obolibrary.org/obo/MONDO_0000984
T8 472-474 Disease denotes HS http://purl.obolibrary.org/obo/MONDO_0019350
T9 956-967 Disease denotes thalassemia http://purl.obolibrary.org/obo/MONDO_0000984

Anatomy-MAT

Id Subject Object Predicate Lexical cue mat_id
T1 291-299 Body_part denotes skeleton http://purl.obolibrary.org/obo/MAT_0000032

Anatomy-UBERON

Id Subject Object Predicate Lexical cue uberon_id
T1 139-150 Body_part denotes erythrocyte http://purl.obolibrary.org/obo/CL_0000232
T2 277-290 Body_part denotes cell membrane http://purl.obolibrary.org/obo/GO_0005886
T3 291-299 Body_part denotes skeleton http://purl.obolibrary.org/obo/UBERON_0004288
T4 519-531 Body_part denotes erythrocytes http://purl.obolibrary.org/obo/CL_0000232
T5 819-827 Body_part denotes membrane http://purl.obolibrary.org/obo/GO_0016020|http://purl.obolibrary.org/obo/UBERON_0000094|http://purl.obolibrary.org/obo/UBERON_0000158
T8 888-900 Body_part denotes erythrocytes http://purl.obolibrary.org/obo/CL_0000232

HP-phenotype

Id Subject Object Predicate Lexical cue hp_id
T1 24-37 Phenotype denotes spherocytosis HP:0004444
T2 175-188 Phenotype denotes spherocytosis HP:0004444