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sentences

Id Subject Object Predicate Lexical cue
TextSentencer_T1 0-144 Sentence denotes Elimination of abnormal sialylglycoproteins in fibroblasts with sialidosis and galactosialidosis by normal gene transfer and enzyme replacement.
TextSentencer_T2 145-612 Sentence denotes Sialidosis and galactosialidosis are lysosomal storage diseases caused by the genetic defects of lysosomal sialidase (neuraminidase-1; NEU1) and lysosomal protective protein/cathepsin A (PPCA), respectively, associated with a NEU1 deficiency, excessive accumulation of sialylglycoconjugates, and development of progressive neurosomatic manifestations; in addition, the latter disorder is accompanied by simultaneous deficiencies of beta-galactosidase and cathepsin A.
TextSentencer_T3 613-887 Sentence denotes We demonstrated that a few soluble N-glycosylated proteins carrying sialyloligosaccharides sensitive to glycopeptidase F (GPF) can be specifically detected in cultured fibroblasts from sialidosis and galactosialidosis cases by blotting with a Maackia amurensis (MAM) lectin.
TextSentencer_T4 888-1085 Sentence denotes We also examined the therapeutic effects of normal gene transfer and enzyme replacement by evaluating the decreases in sialylglycoconjugates accumulated in fibroblasts with these NEU1 deficiencies.
TextSentencer_T5 1086-1550 Sentence denotes The specific N-glycosylated proteins detected on MAM lectin blotting as well as the granular lysosomal fluorescence due to an avidin-FITC/biotinylated MAM lectin conjugate in sialidosis and galactosialidosis fibroblasts disappeared in parallel with the restoration of the intracellular NEU1 activity after transfection of the recombinant NEU1 fused to HA tag sequence and the wild-type PPCA cDNA as well as administration of the recombinant PPCA precursor protein.
TextSentencer_T6 1551-1804 Sentence denotes The detection method for the abnormal sialylglycoproteins in cultured cells involving MAM lectin was demonstrated to be useful not only for biochemical and diagnostic analyses of NEU1 deficiencies but also for therapeutic evaluation of these conditions.
T1 0-144 Sentence denotes Elimination of abnormal sialylglycoproteins in fibroblasts with sialidosis and galactosialidosis by normal gene transfer and enzyme replacement.
T2 145-887 Sentence denotes Sialidosis and galactosialidosis are lysosomal storage diseases caused by the genetic defects of lysosomal sialidase (neuraminidase-1; NEU1) and lysosomal protective protein/cathepsin A (PPCA), respectively, associated with a NEU1 deficiency, excessive accumulation of sialylglycoconjugates, and development of progressive neurosomatic manifestations; in addition, the latter disorder is accompanied by simultaneous deficiencies of beta-galactosidase and cathepsin A. We demonstrated that a few soluble N-glycosylated proteins carrying sialyloligosaccharides sensitive to glycopeptidase F (GPF) can be specifically detected in cultured fibroblasts from sialidosis and galactosialidosis cases by blotting with a Maackia amurensis (MAM) lectin.
T3 888-1085 Sentence denotes We also examined the therapeutic effects of normal gene transfer and enzyme replacement by evaluating the decreases in sialylglycoconjugates accumulated in fibroblasts with these NEU1 deficiencies.
T4 1086-1550 Sentence denotes The specific N-glycosylated proteins detected on MAM lectin blotting as well as the granular lysosomal fluorescence due to an avidin-FITC/biotinylated MAM lectin conjugate in sialidosis and galactosialidosis fibroblasts disappeared in parallel with the restoration of the intracellular NEU1 activity after transfection of the recombinant NEU1 fused to HA tag sequence and the wild-type PPCA cDNA as well as administration of the recombinant PPCA precursor protein.
T5 1551-1804 Sentence denotes The detection method for the abnormal sialylglycoproteins in cultured cells involving MAM lectin was demonstrated to be useful not only for biochemical and diagnostic analyses of NEU1 deficiencies but also for therapeutic evaluation of these conditions.
T1 0-144 Sentence denotes Elimination of abnormal sialylglycoproteins in fibroblasts with sialidosis and galactosialidosis by normal gene transfer and enzyme replacement.
T2 145-612 Sentence denotes Sialidosis and galactosialidosis are lysosomal storage diseases caused by the genetic defects of lysosomal sialidase (neuraminidase-1; NEU1) and lysosomal protective protein/cathepsin A (PPCA), respectively, associated with a NEU1 deficiency, excessive accumulation of sialylglycoconjugates, and development of progressive neurosomatic manifestations; in addition, the latter disorder is accompanied by simultaneous deficiencies of beta-galactosidase and cathepsin A.
T3 613-887 Sentence denotes We demonstrated that a few soluble N-glycosylated proteins carrying sialyloligosaccharides sensitive to glycopeptidase F (GPF) can be specifically detected in cultured fibroblasts from sialidosis and galactosialidosis cases by blotting with a Maackia amurensis (MAM) lectin.
T4 888-1085 Sentence denotes We also examined the therapeutic effects of normal gene transfer and enzyme replacement by evaluating the decreases in sialylglycoconjugates accumulated in fibroblasts with these NEU1 deficiencies.
T5 1086-1550 Sentence denotes The specific N-glycosylated proteins detected on MAM lectin blotting as well as the granular lysosomal fluorescence due to an avidin-FITC/biotinylated MAM lectin conjugate in sialidosis and galactosialidosis fibroblasts disappeared in parallel with the restoration of the intracellular NEU1 activity after transfection of the recombinant NEU1 fused to HA tag sequence and the wild-type PPCA cDNA as well as administration of the recombinant PPCA precursor protein.
T6 1551-1804 Sentence denotes The detection method for the abnormal sialylglycoproteins in cultured cells involving MAM lectin was demonstrated to be useful not only for biochemical and diagnostic analyses of NEU1 deficiencies but also for therapeutic evaluation of these conditions.

GlycoBiology-GDGDB

Id Subject Object Predicate Lexical cue
_T1 280-284 http://acgg.asia/db/diseases/gdgdb?con_ui=CON00012 denotes NEU1
_T2 280-284 http://acgg.asia/db/diseases/gdgdb?con_ui=CON00013 denotes NEU1
_T3 280-284 http://acgg.asia/db/diseases/gdgdb?con_ui=CON00014 denotes NEU1
_T4 280-284 http://acgg.asia/db/diseases/gdgdb?con_ui=CON00015 denotes NEU1
_T5 280-284 http://acgg.asia/db/diseases/gdgdb?con_ui=CON00016 denotes NEU1
_T6 280-284 http://acgg.asia/db/diseases/gdgdb?con_ui=CON00017 denotes NEU1
_T7 371-375 http://acgg.asia/db/diseases/gdgdb?con_ui=CON00012 denotes NEU1
_T8 371-375 http://acgg.asia/db/diseases/gdgdb?con_ui=CON00013 denotes NEU1
_T9 371-375 http://acgg.asia/db/diseases/gdgdb?con_ui=CON00014 denotes NEU1
_T10 371-375 http://acgg.asia/db/diseases/gdgdb?con_ui=CON00015 denotes NEU1
_T11 371-375 http://acgg.asia/db/diseases/gdgdb?con_ui=CON00016 denotes NEU1
_T12 371-375 http://acgg.asia/db/diseases/gdgdb?con_ui=CON00017 denotes NEU1
_T13 1067-1071 http://acgg.asia/db/diseases/gdgdb?con_ui=CON00012 denotes NEU1
_T14 1067-1071 http://acgg.asia/db/diseases/gdgdb?con_ui=CON00013 denotes NEU1
_T15 1067-1071 http://acgg.asia/db/diseases/gdgdb?con_ui=CON00014 denotes NEU1
_T16 1067-1071 http://acgg.asia/db/diseases/gdgdb?con_ui=CON00015 denotes NEU1
_T17 1067-1071 http://acgg.asia/db/diseases/gdgdb?con_ui=CON00016 denotes NEU1
_T18 1067-1071 http://acgg.asia/db/diseases/gdgdb?con_ui=CON00017 denotes NEU1
_T19 1372-1376 http://acgg.asia/db/diseases/gdgdb?con_ui=CON00012 denotes NEU1
_T20 1372-1376 http://acgg.asia/db/diseases/gdgdb?con_ui=CON00013 denotes NEU1
_T21 1372-1376 http://acgg.asia/db/diseases/gdgdb?con_ui=CON00014 denotes NEU1
_T22 1372-1376 http://acgg.asia/db/diseases/gdgdb?con_ui=CON00015 denotes NEU1
_T23 1372-1376 http://acgg.asia/db/diseases/gdgdb?con_ui=CON00016 denotes NEU1
_T24 1372-1376 http://acgg.asia/db/diseases/gdgdb?con_ui=CON00017 denotes NEU1
_T25 1424-1428 http://acgg.asia/db/diseases/gdgdb?con_ui=CON00012 denotes NEU1
_T26 1424-1428 http://acgg.asia/db/diseases/gdgdb?con_ui=CON00013 denotes NEU1
_T27 1424-1428 http://acgg.asia/db/diseases/gdgdb?con_ui=CON00014 denotes NEU1
_T28 1424-1428 http://acgg.asia/db/diseases/gdgdb?con_ui=CON00015 denotes NEU1
_T29 1424-1428 http://acgg.asia/db/diseases/gdgdb?con_ui=CON00016 denotes NEU1
_T30 1424-1428 http://acgg.asia/db/diseases/gdgdb?con_ui=CON00017 denotes NEU1
_T31 1730-1734 http://acgg.asia/db/diseases/gdgdb?con_ui=CON00012 denotes NEU1
_T32 1730-1734 http://acgg.asia/db/diseases/gdgdb?con_ui=CON00013 denotes NEU1
_T33 1730-1734 http://acgg.asia/db/diseases/gdgdb?con_ui=CON00014 denotes NEU1
_T34 1730-1734 http://acgg.asia/db/diseases/gdgdb?con_ui=CON00015 denotes NEU1
_T35 1730-1734 http://acgg.asia/db/diseases/gdgdb?con_ui=CON00016 denotes NEU1
_T36 1730-1734 http://acgg.asia/db/diseases/gdgdb?con_ui=CON00017 denotes NEU1

uniprot-human

Id Subject Object Predicate Lexical cue
T1 242-261 http://www.uniprot.org/uniprot/Q99519 denotes lysosomal sialidase
T2 280-284 http://www.uniprot.org/uniprot/Q99519 denotes NEU1
T3 371-375 http://www.uniprot.org/uniprot/Q99519 denotes NEU1
T4 1067-1071 http://www.uniprot.org/uniprot/Q99519 denotes NEU1
T5 1372-1376 http://www.uniprot.org/uniprot/Q99519 denotes NEU1
T6 1424-1428 http://www.uniprot.org/uniprot/Q99519 denotes NEU1
T7 1730-1734 http://www.uniprot.org/uniprot/Q99519 denotes NEU1
T8 290-318 http://www.uniprot.org/uniprot/P10619 denotes lysosomal protective protein
T9 332-336 http://www.uniprot.org/uniprot/P10619 denotes PPCA
T10 1472-1476 http://www.uniprot.org/uniprot/P10619 denotes PPCA
T11 600-611 http://www.uniprot.org/uniprot/P10619 denotes cathepsin A
T12 577-595 http://www.uniprot.org/uniprot/P16278 denotes beta-galactosidase
T13 1438-1440 http://www.uniprot.org/uniprot/P69208 denotes HA

uniprot-mouse

Id Subject Object Predicate Lexical cue
T1 242-261 http://www.uniprot.org/uniprot/O35657 denotes lysosomal sialidase
T2 290-318 http://www.uniprot.org/uniprot/P16675 denotes lysosomal protective protein
T3 332-336 http://www.uniprot.org/uniprot/P16675 denotes PPCA
T4 1472-1476 http://www.uniprot.org/uniprot/P16675 denotes PPCA
T5 600-611 http://www.uniprot.org/uniprot/P16675 denotes cathepsin A
T6 577-595 http://www.uniprot.org/uniprot/P23780 denotes beta-galactosidase
T7 1429-1434 http://www.uniprot.org/uniprot/O35625 denotes fused

GlycoBiology-NCBITAXON

Id Subject Object Predicate Lexical cue
T1 577-581 http://purl.bioontology.org/ontology/NCBITAXON/3554 denotes beta
T2 577-581 http://purl.bioontology.org/ontology/NCBITAXON/158455 denotes beta
T3 856-863 http://purl.bioontology.org/ontology/NCBITAXON/37500 denotes Maackia
T4 856-873 http://purl.bioontology.org/ontology/NCBITAXON/37501 denotes Maackia amurensis
T5 1321-1329 http://purl.bioontology.org/ontology/NCBITAXON/871272 denotes parallel
T6 1621-1626 http://purl.bioontology.org/ontology/STY/T025 denotes cells

GO-BP

Id Subject Object Predicate Lexical cue
T1 192-199 http://purl.obolibrary.org/obo/GO_0051235 denotes storage
T2 192-199 http://purl.obolibrary.org/obo/GO_0035732 denotes storage
T3 441-452 http://purl.obolibrary.org/obo/GO_0032502 denotes development
T4 648-671 http://purl.obolibrary.org/obo/GO_0006487 denotes N-glycosylated proteins
T5 1099-1122 http://purl.obolibrary.org/obo/GO_0006487 denotes N-glycosylated proteins
T6 650-662 http://purl.obolibrary.org/obo/GO_0070085 denotes glycosylated
T7 1101-1113 http://purl.obolibrary.org/obo/GO_0070085 denotes glycosylated
T8 650-671 http://purl.obolibrary.org/obo/GO_0006486 denotes glycosylated proteins
T9 1101-1122 http://purl.obolibrary.org/obo/GO_0006486 denotes glycosylated proteins
T10 704-713 http://purl.obolibrary.org/obo/GO_0046960 denotes sensitive
T11 1248-1257 http://purl.obolibrary.org/obo/GO_0000746 denotes conjugate

GO-CC

Id Subject Object Predicate Lexical cue
T1 182-191 http://purl.obolibrary.org/obo/GO_0005764 denotes lysosomal
T2 242-251 http://purl.obolibrary.org/obo/GO_0005764 denotes lysosomal
T3 290-299 http://purl.obolibrary.org/obo/GO_0005764 denotes lysosomal
T4 1179-1188 http://purl.obolibrary.org/obo/GO_0005764 denotes lysosomal
T5 1358-1371 http://purl.obolibrary.org/obo/GO_0005622 denotes intracellular
T6 1621-1626 http://purl.obolibrary.org/obo/GO_0005623 denotes cells

EDAM-topics

Id Subject Object Predicate Lexical cue
T1 182-191 http://edamontology.org/topic_0616 denotes lysosomal
T2 200-208 http://edamontology.org/topic_0634 denotes diseases
T3 223-230 http://edamontology.org/topic_3053 denotes genetic
T4 242-251 http://edamontology.org/topic_0616 denotes lysosomal
T5 290-299 http://edamontology.org/topic_0616 denotes lysosomal
T6 311-318 http://edamontology.org/topic_0078 denotes protein
T7 663-671 http://edamontology.org/topic_0078 denotes proteins
T8 1114-1122 http://edamontology.org/topic_0078 denotes proteins
T9 1114-1131 http://edamontology.org/topic_3074 denotes proteins detected
T10 1179-1188 http://edamontology.org/topic_0616 denotes lysosomal
T11 1445-1453 http://edamontology.org/topic_0080 denotes sequence
T12 1445-1453 http://edamontology.org/topic_3168 denotes sequence
T13 1477-1481 http://edamontology.org/topic_3512 denotes cDNA
T14 1542-1549 http://edamontology.org/topic_0078 denotes protein

EDAM-DFO

Id Subject Object Predicate Lexical cue
T1 100-106 http://edamontology.org/operation_3435 denotes normal
T2 300-318 http://edamontology.org/format_1219 denotes protective protein
T3 311-318 http://edamontology.org/format_1208 denotes protein
T4 311-318 http://edamontology.org/data_1467 denotes protein
T5 616-628 http://edamontology.org/operation_2246 denotes demonstrated
T6 663-671 http://edamontology.org/data_1467 denotes proteins
T7 663-671 http://edamontology.org/format_1208 denotes proteins
T8 760-768 http://edamontology.org/operation_2423 denotes detected
T9 932-938 http://edamontology.org/operation_3435 denotes normal
T10 1114-1122 http://edamontology.org/data_1467 denotes proteins
T11 1114-1122 http://edamontology.org/format_1208 denotes proteins
T12 1114-1131 http://edamontology.org/operation_3087 denotes proteins detected
T13 1114-1131 http://edamontology.org/operation_3092 denotes proteins detected
T14 1123-1131 http://edamontology.org/operation_2423 denotes detected
T15 1445-1453 http://edamontology.org/data_2044 denotes sequence
T16 1445-1453 http://edamontology.org/operation_3218 denotes sequence
T17 1542-1549 http://edamontology.org/data_1467 denotes protein
T18 1542-1549 http://edamontology.org/format_1208 denotes protein
T19 1555-1564 http://edamontology.org/operation_2423 denotes detection
T20 1652-1664 http://edamontology.org/operation_2246 denotes demonstrated

DisGeNET5_gene_disease

Id Subject Object Predicate Lexical cue
16361247-1#432#450#gene2720 577-595 gene2720 denotes beta-galactosidase
16361247-1#97#116#gene4758 242-261 gene4758 denotes lysosomal sialidase
16361247-1#118#133#gene4758 263-278 gene4758 denotes neuraminidase-1
16361247-1#135#139#gene4758 280-284 gene4758 denotes NEU1
16361247-1#145#173#gene5476 290-318 gene5476 denotes lysosomal protective protein
16361247-1#174#185#gene5476 319-330 gene5476 denotes cathepsin A
16361247-1#432#450#gene2720 577-595 gene2720 denotes beta-galactosidase
16361247-1#455#466#gene5476 600-611 gene5476 denotes cathepsin A
16361247-1#0#10#diseaseC0026697 145-155 diseaseC0026697 denotes Sialidosis
16361247-1#0#10#diseaseC0268226 145-155 diseaseC0268226 denotes Sialidosis
16361247-1#226#241#diseaseC0268228 371-386 diseaseC0268228 denotes NEU1 deficiency
16361247-1#15#32#diseaseC0268233 160-177 diseaseC0268233 denotes galactosialidosis
16361247-1#226#241#diseaseC0268228 371-386 diseaseC0268228 denotes NEU1 deficiency
16361247-1#15#32#diseaseC0268233 160-177 diseaseC0268233 denotes galactosialidosis
16361247-1#226#241#diseaseC0268228 371-386 diseaseC0268228 denotes NEU1 deficiency
16361247-1#15#32#diseaseC0268233 160-177 diseaseC0268233 denotes galactosialidosis
16361247-1#37#63#diseaseC0085078 182-208 diseaseC0085078 denotes lysosomal storage diseases
16361247-1#226#241#diseaseC0268228 371-386 diseaseC0268228 denotes NEU1 deficiency
16361247-1#15#32#diseaseC0268233 160-177 diseaseC0268233 denotes galactosialidosis
16361247-1#37#63#diseaseC0085078 182-208 diseaseC0085078 denotes lysosomal storage diseases
16361247-4#286#290#gene4758 1372-1376 gene4758 denotes NEU1
16361247-4#338#342#gene4758 1424-1428 gene4758 denotes NEU1
16361247-4#286#290#gene4758 1372-1376 gene4758 denotes NEU1
16361247-4#338#342#gene4758 1424-1428 gene4758 denotes NEU1
16361247-4#175#185#diseaseC0026697 1261-1271 diseaseC0026697 denotes sialidosis
16361247-4#175#185#diseaseC0268226 1261-1271 diseaseC0268226 denotes sialidosis
16361247-4#175#185#diseaseC0026697 1261-1271 diseaseC0026697 denotes sialidosis
16361247-4#175#185#diseaseC0268226 1261-1271 diseaseC0268226 denotes sialidosis
16361247-4#190#207#diseaseC0268233 1276-1293 diseaseC0268233 denotes galactosialidosis
432#450#gene27200#10#diseaseC0026697 16361247-1#432#450#gene2720 16361247-1#0#10#diseaseC0026697 associated_with beta-galactosidase,Sialidosis
432#450#gene27200#10#diseaseC0268226 16361247-1#432#450#gene2720 16361247-1#0#10#diseaseC0268226 associated_with beta-galactosidase,Sialidosis
432#450#gene2720226#241#diseaseC0268228 16361247-1#432#450#gene2720 16361247-1#226#241#diseaseC0268228 associated_with beta-galactosidase,NEU1 deficiency
432#450#gene272015#32#diseaseC0268233 16361247-1#432#450#gene2720 16361247-1#15#32#diseaseC0268233 associated_with beta-galactosidase,galactosialidosis
432#450#gene2720226#241#diseaseC0268228 16361247-1#432#450#gene2720 16361247-1#226#241#diseaseC0268228 associated_with beta-galactosidase,NEU1 deficiency
432#450#gene272015#32#diseaseC0268233 16361247-1#432#450#gene2720 16361247-1#15#32#diseaseC0268233 associated_with beta-galactosidase,galactosialidosis
432#450#gene2720226#241#diseaseC0268228 16361247-1#432#450#gene2720 16361247-1#226#241#diseaseC0268228 associated_with beta-galactosidase,NEU1 deficiency
432#450#gene272015#32#diseaseC0268233 16361247-1#432#450#gene2720 16361247-1#15#32#diseaseC0268233 associated_with beta-galactosidase,galactosialidosis
432#450#gene272037#63#diseaseC0085078 16361247-1#432#450#gene2720 16361247-1#37#63#diseaseC0085078 associated_with beta-galactosidase,lysosomal storage diseases
432#450#gene2720226#241#diseaseC0268228 16361247-1#432#450#gene2720 16361247-1#226#241#diseaseC0268228 associated_with beta-galactosidase,NEU1 deficiency
432#450#gene272015#32#diseaseC0268233 16361247-1#432#450#gene2720 16361247-1#15#32#diseaseC0268233 associated_with beta-galactosidase,galactosialidosis
432#450#gene272037#63#diseaseC0085078 16361247-1#432#450#gene2720 16361247-1#37#63#diseaseC0085078 associated_with beta-galactosidase,lysosomal storage diseases
97#116#gene47580#10#diseaseC0026697 16361247-1#97#116#gene4758 16361247-1#0#10#diseaseC0026697 associated_with lysosomal sialidase,Sialidosis
97#116#gene47580#10#diseaseC0268226 16361247-1#97#116#gene4758 16361247-1#0#10#diseaseC0268226 associated_with lysosomal sialidase,Sialidosis
97#116#gene4758226#241#diseaseC0268228 16361247-1#97#116#gene4758 16361247-1#226#241#diseaseC0268228 associated_with lysosomal sialidase,NEU1 deficiency
97#116#gene475815#32#diseaseC0268233 16361247-1#97#116#gene4758 16361247-1#15#32#diseaseC0268233 associated_with lysosomal sialidase,galactosialidosis
97#116#gene4758226#241#diseaseC0268228 16361247-1#97#116#gene4758 16361247-1#226#241#diseaseC0268228 associated_with lysosomal sialidase,NEU1 deficiency
97#116#gene475815#32#diseaseC0268233 16361247-1#97#116#gene4758 16361247-1#15#32#diseaseC0268233 associated_with lysosomal sialidase,galactosialidosis
97#116#gene4758226#241#diseaseC0268228 16361247-1#97#116#gene4758 16361247-1#226#241#diseaseC0268228 associated_with lysosomal sialidase,NEU1 deficiency
97#116#gene475815#32#diseaseC0268233 16361247-1#97#116#gene4758 16361247-1#15#32#diseaseC0268233 associated_with lysosomal sialidase,galactosialidosis
97#116#gene475837#63#diseaseC0085078 16361247-1#97#116#gene4758 16361247-1#37#63#diseaseC0085078 associated_with lysosomal sialidase,lysosomal storage diseases
97#116#gene4758226#241#diseaseC0268228 16361247-1#97#116#gene4758 16361247-1#226#241#diseaseC0268228 associated_with lysosomal sialidase,NEU1 deficiency
97#116#gene475815#32#diseaseC0268233 16361247-1#97#116#gene4758 16361247-1#15#32#diseaseC0268233 associated_with lysosomal sialidase,galactosialidosis
97#116#gene475837#63#diseaseC0085078 16361247-1#97#116#gene4758 16361247-1#37#63#diseaseC0085078 associated_with lysosomal sialidase,lysosomal storage diseases
118#133#gene47580#10#diseaseC0026697 16361247-1#118#133#gene4758 16361247-1#0#10#diseaseC0026697 associated_with neuraminidase-1,Sialidosis
118#133#gene47580#10#diseaseC0268226 16361247-1#118#133#gene4758 16361247-1#0#10#diseaseC0268226 associated_with neuraminidase-1,Sialidosis
118#133#gene4758226#241#diseaseC0268228 16361247-1#118#133#gene4758 16361247-1#226#241#diseaseC0268228 associated_with neuraminidase-1,NEU1 deficiency
118#133#gene475815#32#diseaseC0268233 16361247-1#118#133#gene4758 16361247-1#15#32#diseaseC0268233 associated_with neuraminidase-1,galactosialidosis
118#133#gene4758226#241#diseaseC0268228 16361247-1#118#133#gene4758 16361247-1#226#241#diseaseC0268228 associated_with neuraminidase-1,NEU1 deficiency
118#133#gene475815#32#diseaseC0268233 16361247-1#118#133#gene4758 16361247-1#15#32#diseaseC0268233 associated_with neuraminidase-1,galactosialidosis
118#133#gene4758226#241#diseaseC0268228 16361247-1#118#133#gene4758 16361247-1#226#241#diseaseC0268228 associated_with neuraminidase-1,NEU1 deficiency
118#133#gene475815#32#diseaseC0268233 16361247-1#118#133#gene4758 16361247-1#15#32#diseaseC0268233 associated_with neuraminidase-1,galactosialidosis
118#133#gene475837#63#diseaseC0085078 16361247-1#118#133#gene4758 16361247-1#37#63#diseaseC0085078 associated_with neuraminidase-1,lysosomal storage diseases
118#133#gene4758226#241#diseaseC0268228 16361247-1#118#133#gene4758 16361247-1#226#241#diseaseC0268228 associated_with neuraminidase-1,NEU1 deficiency
118#133#gene475815#32#diseaseC0268233 16361247-1#118#133#gene4758 16361247-1#15#32#diseaseC0268233 associated_with neuraminidase-1,galactosialidosis
118#133#gene475837#63#diseaseC0085078 16361247-1#118#133#gene4758 16361247-1#37#63#diseaseC0085078 associated_with neuraminidase-1,lysosomal storage diseases
135#139#gene47580#10#diseaseC0026697 16361247-1#135#139#gene4758 16361247-1#0#10#diseaseC0026697 associated_with NEU1,Sialidosis
135#139#gene47580#10#diseaseC0268226 16361247-1#135#139#gene4758 16361247-1#0#10#diseaseC0268226 associated_with NEU1,Sialidosis
135#139#gene4758226#241#diseaseC0268228 16361247-1#135#139#gene4758 16361247-1#226#241#diseaseC0268228 associated_with NEU1,NEU1 deficiency
135#139#gene475815#32#diseaseC0268233 16361247-1#135#139#gene4758 16361247-1#15#32#diseaseC0268233 associated_with NEU1,galactosialidosis
135#139#gene4758226#241#diseaseC0268228 16361247-1#135#139#gene4758 16361247-1#226#241#diseaseC0268228 associated_with NEU1,NEU1 deficiency
135#139#gene475815#32#diseaseC0268233 16361247-1#135#139#gene4758 16361247-1#15#32#diseaseC0268233 associated_with NEU1,galactosialidosis
135#139#gene4758226#241#diseaseC0268228 16361247-1#135#139#gene4758 16361247-1#226#241#diseaseC0268228 associated_with NEU1,NEU1 deficiency
135#139#gene475815#32#diseaseC0268233 16361247-1#135#139#gene4758 16361247-1#15#32#diseaseC0268233 associated_with NEU1,galactosialidosis
135#139#gene475837#63#diseaseC0085078 16361247-1#135#139#gene4758 16361247-1#37#63#diseaseC0085078 associated_with NEU1,lysosomal storage diseases
135#139#gene4758226#241#diseaseC0268228 16361247-1#135#139#gene4758 16361247-1#226#241#diseaseC0268228 associated_with NEU1,NEU1 deficiency
135#139#gene475815#32#diseaseC0268233 16361247-1#135#139#gene4758 16361247-1#15#32#diseaseC0268233 associated_with NEU1,galactosialidosis
135#139#gene475837#63#diseaseC0085078 16361247-1#135#139#gene4758 16361247-1#37#63#diseaseC0085078 associated_with NEU1,lysosomal storage diseases
145#173#gene54760#10#diseaseC0026697 16361247-1#145#173#gene5476 16361247-1#0#10#diseaseC0026697 associated_with lysosomal protective protein,Sialidosis
145#173#gene54760#10#diseaseC0268226 16361247-1#145#173#gene5476 16361247-1#0#10#diseaseC0268226 associated_with lysosomal protective protein,Sialidosis
145#173#gene5476226#241#diseaseC0268228 16361247-1#145#173#gene5476 16361247-1#226#241#diseaseC0268228 associated_with lysosomal protective protein,NEU1 deficiency
145#173#gene547615#32#diseaseC0268233 16361247-1#145#173#gene5476 16361247-1#15#32#diseaseC0268233 associated_with lysosomal protective protein,galactosialidosis
145#173#gene5476226#241#diseaseC0268228 16361247-1#145#173#gene5476 16361247-1#226#241#diseaseC0268228 associated_with lysosomal protective protein,NEU1 deficiency
145#173#gene547615#32#diseaseC0268233 16361247-1#145#173#gene5476 16361247-1#15#32#diseaseC0268233 associated_with lysosomal protective protein,galactosialidosis
145#173#gene5476226#241#diseaseC0268228 16361247-1#145#173#gene5476 16361247-1#226#241#diseaseC0268228 associated_with lysosomal protective protein,NEU1 deficiency
145#173#gene547615#32#diseaseC0268233 16361247-1#145#173#gene5476 16361247-1#15#32#diseaseC0268233 associated_with lysosomal protective protein,galactosialidosis
145#173#gene547637#63#diseaseC0085078 16361247-1#145#173#gene5476 16361247-1#37#63#diseaseC0085078 associated_with lysosomal protective protein,lysosomal storage diseases
145#173#gene5476226#241#diseaseC0268228 16361247-1#145#173#gene5476 16361247-1#226#241#diseaseC0268228 associated_with lysosomal protective protein,NEU1 deficiency
145#173#gene547615#32#diseaseC0268233 16361247-1#145#173#gene5476 16361247-1#15#32#diseaseC0268233 associated_with lysosomal protective protein,galactosialidosis
145#173#gene547637#63#diseaseC0085078 16361247-1#145#173#gene5476 16361247-1#37#63#diseaseC0085078 associated_with lysosomal protective protein,lysosomal storage diseases
174#185#gene54760#10#diseaseC0026697 16361247-1#174#185#gene5476 16361247-1#0#10#diseaseC0026697 associated_with cathepsin A,Sialidosis
174#185#gene54760#10#diseaseC0268226 16361247-1#174#185#gene5476 16361247-1#0#10#diseaseC0268226 associated_with cathepsin A,Sialidosis
174#185#gene5476226#241#diseaseC0268228 16361247-1#174#185#gene5476 16361247-1#226#241#diseaseC0268228 associated_with cathepsin A,NEU1 deficiency
174#185#gene547615#32#diseaseC0268233 16361247-1#174#185#gene5476 16361247-1#15#32#diseaseC0268233 associated_with cathepsin A,galactosialidosis
174#185#gene5476226#241#diseaseC0268228 16361247-1#174#185#gene5476 16361247-1#226#241#diseaseC0268228 associated_with cathepsin A,NEU1 deficiency
174#185#gene547615#32#diseaseC0268233 16361247-1#174#185#gene5476 16361247-1#15#32#diseaseC0268233 associated_with cathepsin A,galactosialidosis
174#185#gene5476226#241#diseaseC0268228 16361247-1#174#185#gene5476 16361247-1#226#241#diseaseC0268228 associated_with cathepsin A,NEU1 deficiency
174#185#gene547615#32#diseaseC0268233 16361247-1#174#185#gene5476 16361247-1#15#32#diseaseC0268233 associated_with cathepsin A,galactosialidosis
174#185#gene547637#63#diseaseC0085078 16361247-1#174#185#gene5476 16361247-1#37#63#diseaseC0085078 associated_with cathepsin A,lysosomal storage diseases
174#185#gene5476226#241#diseaseC0268228 16361247-1#174#185#gene5476 16361247-1#226#241#diseaseC0268228 associated_with cathepsin A,NEU1 deficiency
174#185#gene547615#32#diseaseC0268233 16361247-1#174#185#gene5476 16361247-1#15#32#diseaseC0268233 associated_with cathepsin A,galactosialidosis
174#185#gene547637#63#diseaseC0085078 16361247-1#174#185#gene5476 16361247-1#37#63#diseaseC0085078 associated_with cathepsin A,lysosomal storage diseases
432#450#gene27200#10#diseaseC0026697 16361247-1#432#450#gene2720 16361247-1#0#10#diseaseC0026697 associated_with beta-galactosidase,Sialidosis
432#450#gene27200#10#diseaseC0268226 16361247-1#432#450#gene2720 16361247-1#0#10#diseaseC0268226 associated_with beta-galactosidase,Sialidosis
432#450#gene2720226#241#diseaseC0268228 16361247-1#432#450#gene2720 16361247-1#226#241#diseaseC0268228 associated_with beta-galactosidase,NEU1 deficiency
432#450#gene272015#32#diseaseC0268233 16361247-1#432#450#gene2720 16361247-1#15#32#diseaseC0268233 associated_with beta-galactosidase,galactosialidosis
432#450#gene2720226#241#diseaseC0268228 16361247-1#432#450#gene2720 16361247-1#226#241#diseaseC0268228 associated_with beta-galactosidase,NEU1 deficiency
432#450#gene272015#32#diseaseC0268233 16361247-1#432#450#gene2720 16361247-1#15#32#diseaseC0268233 associated_with beta-galactosidase,galactosialidosis
432#450#gene2720226#241#diseaseC0268228 16361247-1#432#450#gene2720 16361247-1#226#241#diseaseC0268228 associated_with beta-galactosidase,NEU1 deficiency
432#450#gene272015#32#diseaseC0268233 16361247-1#432#450#gene2720 16361247-1#15#32#diseaseC0268233 associated_with beta-galactosidase,galactosialidosis
432#450#gene272037#63#diseaseC0085078 16361247-1#432#450#gene2720 16361247-1#37#63#diseaseC0085078 associated_with beta-galactosidase,lysosomal storage diseases
432#450#gene2720226#241#diseaseC0268228 16361247-1#432#450#gene2720 16361247-1#226#241#diseaseC0268228 associated_with beta-galactosidase,NEU1 deficiency
432#450#gene272015#32#diseaseC0268233 16361247-1#432#450#gene2720 16361247-1#15#32#diseaseC0268233 associated_with beta-galactosidase,galactosialidosis
432#450#gene272037#63#diseaseC0085078 16361247-1#432#450#gene2720 16361247-1#37#63#diseaseC0085078 associated_with beta-galactosidase,lysosomal storage diseases
455#466#gene54760#10#diseaseC0026697 16361247-1#455#466#gene5476 16361247-1#0#10#diseaseC0026697 associated_with cathepsin A,Sialidosis
455#466#gene54760#10#diseaseC0268226 16361247-1#455#466#gene5476 16361247-1#0#10#diseaseC0268226 associated_with cathepsin A,Sialidosis
455#466#gene5476226#241#diseaseC0268228 16361247-1#455#466#gene5476 16361247-1#226#241#diseaseC0268228 associated_with cathepsin A,NEU1 deficiency
455#466#gene547615#32#diseaseC0268233 16361247-1#455#466#gene5476 16361247-1#15#32#diseaseC0268233 associated_with cathepsin A,galactosialidosis
455#466#gene5476226#241#diseaseC0268228 16361247-1#455#466#gene5476 16361247-1#226#241#diseaseC0268228 associated_with cathepsin A,NEU1 deficiency
455#466#gene547615#32#diseaseC0268233 16361247-1#455#466#gene5476 16361247-1#15#32#diseaseC0268233 associated_with cathepsin A,galactosialidosis
455#466#gene5476226#241#diseaseC0268228 16361247-1#455#466#gene5476 16361247-1#226#241#diseaseC0268228 associated_with cathepsin A,NEU1 deficiency
455#466#gene547615#32#diseaseC0268233 16361247-1#455#466#gene5476 16361247-1#15#32#diseaseC0268233 associated_with cathepsin A,galactosialidosis
455#466#gene547637#63#diseaseC0085078 16361247-1#455#466#gene5476 16361247-1#37#63#diseaseC0085078 associated_with cathepsin A,lysosomal storage diseases
455#466#gene5476226#241#diseaseC0268228 16361247-1#455#466#gene5476 16361247-1#226#241#diseaseC0268228 associated_with cathepsin A,NEU1 deficiency
455#466#gene547615#32#diseaseC0268233 16361247-1#455#466#gene5476 16361247-1#15#32#diseaseC0268233 associated_with cathepsin A,galactosialidosis
455#466#gene547637#63#diseaseC0085078 16361247-1#455#466#gene5476 16361247-1#37#63#diseaseC0085078 associated_with cathepsin A,lysosomal storage diseases
286#290#gene4758175#185#diseaseC0026697 16361247-4#286#290#gene4758 16361247-4#175#185#diseaseC0026697 associated_with NEU1,sialidosis
286#290#gene4758175#185#diseaseC0268226 16361247-4#286#290#gene4758 16361247-4#175#185#diseaseC0268226 associated_with NEU1,sialidosis
286#290#gene4758175#185#diseaseC0026697 16361247-4#286#290#gene4758 16361247-4#175#185#diseaseC0026697 associated_with NEU1,sialidosis
286#290#gene4758175#185#diseaseC0268226 16361247-4#286#290#gene4758 16361247-4#175#185#diseaseC0268226 associated_with NEU1,sialidosis
286#290#gene4758190#207#diseaseC0268233 16361247-4#286#290#gene4758 16361247-4#190#207#diseaseC0268233 associated_with NEU1,galactosialidosis
338#342#gene4758175#185#diseaseC0026697 16361247-4#338#342#gene4758 16361247-4#175#185#diseaseC0026697 associated_with NEU1,sialidosis
338#342#gene4758175#185#diseaseC0268226 16361247-4#338#342#gene4758 16361247-4#175#185#diseaseC0268226 associated_with NEU1,sialidosis
338#342#gene4758175#185#diseaseC0026697 16361247-4#338#342#gene4758 16361247-4#175#185#diseaseC0026697 associated_with NEU1,sialidosis
338#342#gene4758175#185#diseaseC0268226 16361247-4#338#342#gene4758 16361247-4#175#185#diseaseC0268226 associated_with NEU1,sialidosis
338#342#gene4758190#207#diseaseC0268233 16361247-4#338#342#gene4758 16361247-4#190#207#diseaseC0268233 associated_with NEU1,galactosialidosis
286#290#gene4758175#185#diseaseC0026697 16361247-4#286#290#gene4758 16361247-4#175#185#diseaseC0026697 associated_with NEU1,sialidosis
286#290#gene4758175#185#diseaseC0268226 16361247-4#286#290#gene4758 16361247-4#175#185#diseaseC0268226 associated_with NEU1,sialidosis
286#290#gene4758175#185#diseaseC0026697 16361247-4#286#290#gene4758 16361247-4#175#185#diseaseC0026697 associated_with NEU1,sialidosis
286#290#gene4758175#185#diseaseC0268226 16361247-4#286#290#gene4758 16361247-4#175#185#diseaseC0268226 associated_with NEU1,sialidosis
286#290#gene4758190#207#diseaseC0268233 16361247-4#286#290#gene4758 16361247-4#190#207#diseaseC0268233 associated_with NEU1,galactosialidosis
338#342#gene4758175#185#diseaseC0026697 16361247-4#338#342#gene4758 16361247-4#175#185#diseaseC0026697 associated_with NEU1,sialidosis
338#342#gene4758175#185#diseaseC0268226 16361247-4#338#342#gene4758 16361247-4#175#185#diseaseC0268226 associated_with NEU1,sialidosis
338#342#gene4758175#185#diseaseC0026697 16361247-4#338#342#gene4758 16361247-4#175#185#diseaseC0026697 associated_with NEU1,sialidosis
338#342#gene4758175#185#diseaseC0268226 16361247-4#338#342#gene4758 16361247-4#175#185#diseaseC0268226 associated_with NEU1,sialidosis
338#342#gene4758190#207#diseaseC0268233 16361247-4#338#342#gene4758 16361247-4#190#207#diseaseC0268233 associated_with NEU1,galactosialidosis

GlycoBiology-MAT

Id Subject Object Predicate Lexical cue
T1 514-520 http://purl.obolibrary.org/obo/MAT_0000488 denotes latter

Lectin

Id Subject Object Predicate Lexical cue
Lectin_T1 875-878 https://acgg.asia/db/lfdb/LfDB0228 denotes MAM
Lectin_T2 1135-1138 https://acgg.asia/db/lfdb/LfDB0228 denotes MAM
Lectin_T3 1237-1240 https://acgg.asia/db/lfdb/LfDB0228 denotes MAM
Lectin_T4 1637-1640 https://acgg.asia/db/lfdb/LfDB0228 denotes MAM

DisGeNET

Id Subject Object Predicate Lexical cue
T0 242-261 gene:4758 denotes lysosomal sialidase
T1 160-177 disease:C0268233 denotes galactosialidosis
T2 242-261 gene:4758 denotes lysosomal sialidase
T3 182-208 disease:C0085078 denotes lysosomal storage diseases
T4 242-261 gene:4758 denotes lysosomal sialidase
T5 371-386 disease:C0268228 denotes NEU1 deficiency
T6 280-284 gene:4758 denotes NEU1
T7 160-177 disease:C0268233 denotes galactosialidosis
T8 280-284 gene:51162 denotes NEU1
T9 160-177 disease:C0268233 denotes galactosialidosis
T10 280-284 gene:4758 denotes NEU1
T11 182-208 disease:C0085078 denotes lysosomal storage diseases
T12 280-284 gene:51162 denotes NEU1
T13 182-208 disease:C0085078 denotes lysosomal storage diseases
T14 280-284 gene:4758 denotes NEU1
T15 371-386 disease:C0268228 denotes NEU1 deficiency
T16 280-284 gene:51162 denotes NEU1
T17 371-386 disease:C0268228 denotes NEU1 deficiency
T18 290-318 gene:5476 denotes lysosomal protective protein
T19 160-177 disease:C0268233 denotes galactosialidosis
T20 290-318 gene:5476 denotes lysosomal protective protein
T21 371-386 disease:C0268228 denotes NEU1 deficiency
T22 319-330 gene:5476 denotes cathepsin A
T23 160-177 disease:C0268233 denotes galactosialidosis
T24 600-611 gene:5476 denotes cathepsin A
T25 371-386 disease:C0268228 denotes NEU1 deficiency
T26 577-595 gene:2720 denotes beta-galactosidase
T27 160-177 disease:C0268233 denotes galactosialidosis
T28 577-595 gene:2720 denotes beta-galactosidase
T29 182-208 disease:C0085078 denotes lysosomal storage diseases
T30 577-595 gene:2720 denotes beta-galactosidase
T31 371-386 disease:C0268228 denotes NEU1 deficiency
T32 600-611 gene:5476 denotes cathepsin A
T33 160-177 disease:C0268233 denotes galactosialidosis
T34 600-611 gene:5476 denotes cathepsin A
T35 182-208 disease:C0085078 denotes lysosomal storage diseases
T36 319-330 gene:5476 denotes cathepsin A
T37 371-386 disease:C0268228 denotes NEU1 deficiency
T38 1372-1376 gene:4758 denotes NEU1
T39 1261-1271 disease:C0268226 denotes sialidosis
T40 1372-1376 gene:51162 denotes NEU1
T41 1261-1271 disease:C0268226 denotes sialidosis
T42 1372-1376 gene:4758 denotes NEU1
T43 1276-1293 disease:C0268233 denotes galactosialidosis
T44 1372-1376 gene:51162 denotes NEU1
T45 1276-1293 disease:C0268233 denotes galactosialidosis
T46 1424-1428 gene:4758 denotes NEU1
T47 1276-1293 disease:C0268233 denotes galactosialidosis
T48 1424-1428 gene:51162 denotes NEU1
T49 1276-1293 disease:C0268233 denotes galactosialidosis
R1 T0 T1 associated_with lysosomal sialidase,galactosialidosis
R2 T2 T3 associated_with lysosomal sialidase,lysosomal storage diseases
R3 T4 T5 associated_with lysosomal sialidase,NEU1 deficiency
R4 T6 T7 associated_with NEU1,galactosialidosis
R5 T8 T9 associated_with NEU1,galactosialidosis
R6 T10 T11 associated_with NEU1,lysosomal storage diseases
R7 T12 T13 associated_with NEU1,lysosomal storage diseases
R8 T14 T15 associated_with NEU1,NEU1 deficiency
R9 T16 T17 associated_with NEU1,NEU1 deficiency
R10 T18 T19 associated_with lysosomal protective protein,galactosialidosis
R11 T20 T21 associated_with lysosomal protective protein,NEU1 deficiency
R12 T22 T23 associated_with cathepsin A,galactosialidosis
R13 T24 T25 associated_with cathepsin A,NEU1 deficiency
R14 T26 T27 associated_with beta-galactosidase,galactosialidosis
R15 T28 T29 associated_with beta-galactosidase,lysosomal storage diseases
R16 T30 T31 associated_with beta-galactosidase,NEU1 deficiency
R17 T32 T33 associated_with cathepsin A,galactosialidosis
R18 T34 T35 associated_with cathepsin A,lysosomal storage diseases
R19 T36 T37 associated_with cathepsin A,NEU1 deficiency
R20 T38 T39 associated_with NEU1,sialidosis
R21 T40 T41 associated_with NEU1,sialidosis
R22 T42 T43 associated_with NEU1,galactosialidosis
R23 T44 T45 associated_with NEU1,galactosialidosis
R24 T46 T47 associated_with NEU1,galactosialidosis
R25 T48 T49 associated_with NEU1,galactosialidosis

mondo_disease

Id Subject Object Predicate Lexical cue mondo_id
T1 64-74 Disease denotes sialidosis http://purl.obolibrary.org/obo/MONDO_0017734
T2 79-96 Disease denotes galactosialidosis http://purl.obolibrary.org/obo/MONDO_0009737
T3 145-155 Disease denotes Sialidosis http://purl.obolibrary.org/obo/MONDO_0017734
T4 160-177 Disease denotes galactosialidosis http://purl.obolibrary.org/obo/MONDO_0009737
T5 182-208 Disease denotes lysosomal storage diseases http://purl.obolibrary.org/obo/MONDO_0002561
T6 371-386 Disease denotes NEU1 deficiency http://purl.obolibrary.org/obo/MONDO_0009738
T7 561-595 Disease denotes deficiencies of beta-galactosidase http://purl.obolibrary.org/obo/MONDO_0018149
T8 798-808 Disease denotes sialidosis http://purl.obolibrary.org/obo/MONDO_0017734
T9 813-830 Disease denotes galactosialidosis http://purl.obolibrary.org/obo/MONDO_0009737
T10 1067-1084 Disease denotes NEU1 deficiencies http://purl.obolibrary.org/obo/MONDO_0009738
T11 1261-1271 Disease denotes sialidosis http://purl.obolibrary.org/obo/MONDO_0017734
T12 1276-1293 Disease denotes galactosialidosis http://purl.obolibrary.org/obo/MONDO_0009737
T13 1730-1747 Disease denotes NEU1 deficiencies http://purl.obolibrary.org/obo/MONDO_0009738

Lectin-Jamboree

Id Subject Object Predicate Lexical cue
T1 880-886 lectin denotes lectin
T2 1139-1145 lectin denotes lectin
T3 1241-1247 lectin denotes lectin
T4 1641-1647 lectin denotes lectin

Lectin-Jamboree-small

Id Subject Object Predicate Lexical cue glycosmos_id
T1 875-878 Lectin denotes MAM GL_001868
T2 1135-1138 Lectin denotes MAM GL_001868
T3 1237-1240 Lectin denotes MAM GL_001868
T4 1637-1640 Lectin denotes MAM GL_001868

Lectin-Jamboree-Sentence

Id Subject Object Predicate Lexical cue
T1 0-144 Sentence denotes Elimination of abnormal sialylglycoproteins in fibroblasts with sialidosis and galactosialidosis by normal gene transfer and enzyme replacement.
T2 145-887 Sentence denotes Sialidosis and galactosialidosis are lysosomal storage diseases caused by the genetic defects of lysosomal sialidase (neuraminidase-1; NEU1) and lysosomal protective protein/cathepsin A (PPCA), respectively, associated with a NEU1 deficiency, excessive accumulation of sialylglycoconjugates, and development of progressive neurosomatic manifestations; in addition, the latter disorder is accompanied by simultaneous deficiencies of beta-galactosidase and cathepsin A. We demonstrated that a few soluble N-glycosylated proteins carrying sialyloligosaccharides sensitive to glycopeptidase F (GPF) can be specifically detected in cultured fibroblasts from sialidosis and galactosialidosis cases by blotting with a Maackia amurensis (MAM) lectin.
T3 888-1085 Sentence denotes We also examined the therapeutic effects of normal gene transfer and enzyme replacement by evaluating the decreases in sialylglycoconjugates accumulated in fibroblasts with these NEU1 deficiencies.
T4 1086-1550 Sentence denotes The specific N-glycosylated proteins detected on MAM lectin blotting as well as the granular lysosomal fluorescence due to an avidin-FITC/biotinylated MAM lectin conjugate in sialidosis and galactosialidosis fibroblasts disappeared in parallel with the restoration of the intracellular NEU1 activity after transfection of the recombinant NEU1 fused to HA tag sequence and the wild-type PPCA cDNA as well as administration of the recombinant PPCA precursor protein.
T5 1551-1804 Sentence denotes The detection method for the abnormal sialylglycoproteins in cultured cells involving MAM lectin was demonstrated to be useful not only for biochemical and diagnostic analyses of NEU1 deficiencies but also for therapeutic evaluation of these conditions.

NCBITAXON

Id Subject Object Predicate Lexical cue db_id
T1 856-873 OrganismTaxon denotes Maackia amurensis 37501
T2 875-878 OrganismTaxon denotes MAM 37501
T3 1135-1138 OrganismTaxon denotes MAM 37501
T4 1237-1240 OrganismTaxon denotes MAM 37501
T5 1637-1640 OrganismTaxon denotes MAM 37501

Anatomy-UBERON

Id Subject Object Predicate Lexical cue uberon_id
T1 47-58 Body_part denotes fibroblasts http://purl.obolibrary.org/obo/CL_0000057
T2 781-792 Body_part denotes fibroblasts http://purl.obolibrary.org/obo/CL_0000057
T3 1044-1055 Body_part denotes fibroblasts http://purl.obolibrary.org/obo/CL_0000057
T4 1294-1305 Body_part denotes fibroblasts http://purl.obolibrary.org/obo/CL_0000057
T5 1358-1371 Body_part denotes intracellular http://purl.obolibrary.org/obo/GO_0005622

CL-cell

Id Subject Object Predicate Lexical cue cl_id
T1 47-58 Cell denotes fibroblasts http://purl.obolibrary.org/obo/CL:0000057
T2 781-792 Cell denotes fibroblasts http://purl.obolibrary.org/obo/CL:0000057
T3 1044-1055 Cell denotes fibroblasts http://purl.obolibrary.org/obo/CL:0000057
T4 1294-1305 Cell denotes fibroblasts http://purl.obolibrary.org/obo/CL:0000057
T5 1612-1626 Cell denotes cultured cells http://purl.obolibrary.org/obo/CL:0000010