PubMed:12634322
Annnotations
Glycan-Motif
Id | Subject | Object | Predicate | Lexical cue |
---|---|---|---|---|
T1 | 71-78 | https://glytoucan.org/Structures/Glycans/G00021MO | denotes | heparin |
T2 | 71-78 | https://glytoucan.org/Structures/Glycans/G54161DR | denotes | heparin |
T3 | 118-125 | https://glytoucan.org/Structures/Glycans/G00021MO | denotes | heparin |
T4 | 118-125 | https://glytoucan.org/Structures/Glycans/G54161DR | denotes | heparin |
T5 | 194-205 | https://glytoucan.org/Structures/Glycans/G43702JT | denotes | chondroitin |
T6 | 771-792 | https://glytoucan.org/Structures/Glycans/G27025MB | denotes | N-acetylgalactosamine |
T7 | 919-940 | https://glytoucan.org/Structures/Glycans/G27025MB | denotes | N-acetylgalactosamine |
T8 | 1521-1528 | https://glytoucan.org/Structures/Glycans/G00021MO | denotes | heparin |
T9 | 1521-1528 | https://glytoucan.org/Structures/Glycans/G54161DR | denotes | heparin |
GlyCosmos6-Glycan-Motif-Image
Id | Subject | Object | Predicate | Lexical cue | image |
---|---|---|---|---|---|
T1 | 71-78 | Glycan_Motif | denotes | heparin | https://api.glycosmos.org/wurcs2image/0.10.0/png/binary/G54161DR|https://api.glycosmos.org/wurcs2image/0.10.0/png/binary/G00021MO |
T3 | 118-125 | Glycan_Motif | denotes | heparin | https://api.glycosmos.org/wurcs2image/0.10.0/png/binary/G54161DR|https://api.glycosmos.org/wurcs2image/0.10.0/png/binary/G00021MO |
T5 | 194-205 | Glycan_Motif | denotes | chondroitin | https://api.glycosmos.org/wurcs2image/0.10.0/png/binary/G43702JT |
T6 | 771-792 | Glycan_Motif | denotes | N-acetylgalactosamine | https://api.glycosmos.org/wurcs2image/0.10.0/png/binary/G27025MB |
T7 | 919-940 | Glycan_Motif | denotes | N-acetylgalactosamine | https://api.glycosmos.org/wurcs2image/0.10.0/png/binary/G27025MB |
T8 | 1521-1528 | Glycan_Motif | denotes | heparin | https://api.glycosmos.org/wurcs2image/0.10.0/png/binary/G54161DR|https://api.glycosmos.org/wurcs2image/0.10.0/png/binary/G00021MO |
sentences
Id | Subject | Object | Predicate | Lexical cue |
---|---|---|---|---|
TextSentencer_T1 | 0-101 | Sentence | denotes | Glycosaminoglycan structures required for strong binding to midkine, a heparin-binding growth factor. |
TextSentencer_T2 | 102-241 | Sentence | denotes | Midkine (MK), a heparin-binding growth factor, binds strongly to oversulfated structures in chondroitin sulfates (CSs) and heparan sulfate. |
TextSentencer_T3 | 242-404 | Sentence | denotes | To elucidate the carbohydrate structure actually involved in the strong binding, dissected brains from 13-day mouse embryos were incubated with [14C]-glucosamine. |
TextSentencer_T4 | 405-634 | Sentence | denotes | The labeled glycosaminoglycans were fractionated by MK-agarose affinity chromatography to a weakly binding fraction, which was eluted by 0.5 M NaCl, and a strongly binding fraction, which was eluted by higher NaCl concentrations. |
TextSentencer_T5 | 635-875 | Sentence | denotes | Among the unsaturated disaccharides released from the strongly binding fraction by chondroitinase ABC, DeltaDi-diSE with 4,6-disulfated N-acetylgalactosamine accounted for 32.3%, whereas its content was lower in the weakly binding fraction. |
TextSentencer_T6 | 876-1020 | Sentence | denotes | Artificial CS-E structure was formed using N-acetylgalactosamine 4-sulfate 6-O-sulfotransferase purified from squid or recombinant human enzyme. |
TextSentencer_T7 | 1021-1224 | Sentence | denotes | Analysis of the products and their interaction with MK revealed that E units without 3-O-sulfation of glucuronic acid are sufficient for strong binding, provided that they are present as a dense cluster. |
TextSentencer_T8 | 1225-1431 | Sentence | denotes | Among the sulfated disaccharides released by heparitinase digestion, the trisulfated one, DeltaDiHS-triS, was the most abundant in the strongly binding fraction and was lower in the weakly binding fraction. |
TextSentencer_T9 | 1432-1593 | Sentence | denotes | Together with results of previous studies, we concluded that the multivalent trisulfated heparin-like unit is another structure involved in strong binding to MK. |
T1 | 0-101 | Sentence | denotes | Glycosaminoglycan structures required for strong binding to midkine, a heparin-binding growth factor. |
T2 | 102-241 | Sentence | denotes | Midkine (MK), a heparin-binding growth factor, binds strongly to oversulfated structures in chondroitin sulfates (CSs) and heparan sulfate. |
T3 | 242-404 | Sentence | denotes | To elucidate the carbohydrate structure actually involved in the strong binding, dissected brains from 13-day mouse embryos were incubated with [14C]-glucosamine. |
T4 | 405-634 | Sentence | denotes | The labeled glycosaminoglycans were fractionated by MK-agarose affinity chromatography to a weakly binding fraction, which was eluted by 0.5 M NaCl, and a strongly binding fraction, which was eluted by higher NaCl concentrations. |
T5 | 635-875 | Sentence | denotes | Among the unsaturated disaccharides released from the strongly binding fraction by chondroitinase ABC, DeltaDi-diSE with 4,6-disulfated N-acetylgalactosamine accounted for 32.3%, whereas its content was lower in the weakly binding fraction. |
T6 | 876-1020 | Sentence | denotes | Artificial CS-E structure was formed using N-acetylgalactosamine 4-sulfate 6-O-sulfotransferase purified from squid or recombinant human enzyme. |
T7 | 1021-1224 | Sentence | denotes | Analysis of the products and their interaction with MK revealed that E units without 3-O-sulfation of glucuronic acid are sufficient for strong binding, provided that they are present as a dense cluster. |
T8 | 1225-1431 | Sentence | denotes | Among the sulfated disaccharides released by heparitinase digestion, the trisulfated one, DeltaDiHS-triS, was the most abundant in the strongly binding fraction and was lower in the weakly binding fraction. |
T9 | 1432-1593 | Sentence | denotes | Together with results of previous studies, we concluded that the multivalent trisulfated heparin-like unit is another structure involved in strong binding to MK. |
T1 | 0-101 | Sentence | denotes | Glycosaminoglycan structures required for strong binding to midkine, a heparin-binding growth factor. |
T2 | 102-241 | Sentence | denotes | Midkine (MK), a heparin-binding growth factor, binds strongly to oversulfated structures in chondroitin sulfates (CSs) and heparan sulfate. |
T3 | 242-404 | Sentence | denotes | To elucidate the carbohydrate structure actually involved in the strong binding, dissected brains from 13-day mouse embryos were incubated with [14C]-glucosamine. |
T4 | 405-634 | Sentence | denotes | The labeled glycosaminoglycans were fractionated by MK-agarose affinity chromatography to a weakly binding fraction, which was eluted by 0.5 M NaCl, and a strongly binding fraction, which was eluted by higher NaCl concentrations. |
T5 | 635-875 | Sentence | denotes | Among the unsaturated disaccharides released from the strongly binding fraction by chondroitinase ABC, DeltaDi-diSE with 4,6-disulfated N-acetylgalactosamine accounted for 32.3%, whereas its content was lower in the weakly binding fraction. |
T6 | 876-1020 | Sentence | denotes | Artificial CS-E structure was formed using N-acetylgalactosamine 4-sulfate 6-O-sulfotransferase purified from squid or recombinant human enzyme. |
T7 | 1021-1224 | Sentence | denotes | Analysis of the products and their interaction with MK revealed that E units without 3-O-sulfation of glucuronic acid are sufficient for strong binding, provided that they are present as a dense cluster. |
T8 | 1225-1431 | Sentence | denotes | Among the sulfated disaccharides released by heparitinase digestion, the trisulfated one, DeltaDiHS-triS, was the most abundant in the strongly binding fraction and was lower in the weakly binding fraction. |
T9 | 1432-1593 | Sentence | denotes | Together with results of previous studies, we concluded that the multivalent trisulfated heparin-like unit is another structure involved in strong binding to MK. |
GlyCosmos6-Glycan-Motif-Structure
Id | Subject | Object | Predicate | Lexical cue |
---|---|---|---|---|
T1 | 71-78 | https://glytoucan.org/Structures/Glycans/G00021MO | denotes | heparin |
T2 | 71-78 | https://glytoucan.org/Structures/Glycans/G54161DR | denotes | heparin |
T3 | 118-125 | https://glytoucan.org/Structures/Glycans/G00021MO | denotes | heparin |
T4 | 118-125 | https://glytoucan.org/Structures/Glycans/G54161DR | denotes | heparin |
T5 | 194-205 | https://glytoucan.org/Structures/Glycans/G43702JT | denotes | chondroitin |
T6 | 771-792 | https://glytoucan.org/Structures/Glycans/G27025MB | denotes | N-acetylgalactosamine |
T7 | 919-940 | https://glytoucan.org/Structures/Glycans/G27025MB | denotes | N-acetylgalactosamine |
T8 | 1521-1528 | https://glytoucan.org/Structures/Glycans/G00021MO | denotes | heparin |
T9 | 1521-1528 | https://glytoucan.org/Structures/Glycans/G54161DR | denotes | heparin |
Glycosmos6-GlycoEpitope
Id | Subject | Object | Predicate | Lexical cue |
---|---|---|---|---|
T1 | 194-205 | http://www.glycoepitope.jp/epitopes/EP0081 | denotes | chondroitin |
T2 | 225-240 | http://www.glycoepitope.jp/epitopes/EP0086 | denotes | heparan sulfate |
Glycosmos6-MAT
Id | Subject | Object | Predicate | Lexical cue |
---|---|---|---|---|
T1 | 333-339 | http://purl.obolibrary.org/obo/MAT_0000098 | denotes | brains |
T2 | 358-365 | http://purl.obolibrary.org/obo/MAT_0000226 | denotes | embryos |
GlycoBiology-FMA
Id | Subject | Object | Predicate | Lexical cue |
---|---|---|---|---|
_T20 | 392-403 | FMAID:196792 | denotes | glucosamine |
_T1 | 0-17 | FMAID:63011 | denotes | Glycosaminoglycan |
_T2 | 0-17 | FMAID:167395 | denotes | Glycosaminoglycan |
_T3 | 71-78 | FMAID:82839 | denotes | heparin |
_T4 | 71-78 | FMAID:167420 | denotes | heparin |
_T5 | 118-125 | FMAID:167420 | denotes | heparin |
_T6 | 118-125 | FMAID:82839 | denotes | heparin |
_T7 | 194-214 | FMAID:82837 | denotes | chondroitin sulfates |
_T8 | 194-214 | FMAID:196838 | denotes | chondroitin sulfates |
_T9 | 225-232 | FMAID:165191 | denotes | heparan |
_T10 | 225-232 | FMAID:67110 | denotes | heparan |
_T11 | 225-240 | FMAID:167405 | denotes | heparan sulfate |
_T12 | 225-240 | FMAID:63023 | denotes | heparan sulfate |
_T13 | 259-271 | FMAID:197276 | denotes | carbohydrate |
_T14 | 259-271 | FMAID:82737 | denotes | carbohydrate |
_T15 | 333-339 | FMAID:50801 | denotes | brains |
_T16 | 333-339 | FMAID:146514 | denotes | brains |
_T17 | 358-365 | FMAID:169646 | denotes | embryos |
_T18 | 358-365 | FMAID:69068 | denotes | embryos |
_T19 | 392-403 | FMAID:82797 | denotes | glucosamine |
_T21 | 417-435 | FMAID:167395 | denotes | glycosaminoglycans |
_T22 | 417-435 | FMAID:63011 | denotes | glycosaminoglycans |
_T23 | 657-670 | FMAID:82744 | denotes | disaccharides |
_T24 | 657-670 | FMAID:196733 | denotes | disaccharides |
_T25 | 771-792 | FMAID:82786 | denotes | N-acetylgalactosamine |
_T26 | 771-792 | FMAID:196780 | denotes | N-acetylgalactosamine |
_T27 | 919-940 | FMAID:82786 | denotes | N-acetylgalactosamine |
_T28 | 919-940 | FMAID:196780 | denotes | N-acetylgalactosamine |
_T29 | 1123-1138 | FMAID:82798 | denotes | glucuronic acid |
_T30 | 1123-1138 | FMAID:196793 | denotes | glucuronic acid |
_T31 | 1244-1257 | FMAID:82744 | denotes | disaccharides |
_T32 | 1244-1257 | FMAID:196733 | denotes | disaccharides |
_T33 | 1521-1528 | FMAID:167420 | denotes | heparin |
_T34 | 1521-1528 | FMAID:82839 | denotes | heparin |
uniprot-human
Id | Subject | Object | Predicate | Lexical cue |
---|---|---|---|---|
T1 | 60-67 | http://www.uniprot.org/uniprot/P21741 | denotes | midkine |
T2 | 102-109 | http://www.uniprot.org/uniprot/P21741 | denotes | Midkine |
T3 | 111-113 | http://www.uniprot.org/uniprot/P21741 | denotes | MK |
T4 | 457-459 | http://www.uniprot.org/uniprot/P21741 | denotes | MK |
T5 | 1073-1075 | http://www.uniprot.org/uniprot/P21741 | denotes | MK |
T6 | 1590-1592 | http://www.uniprot.org/uniprot/P21741 | denotes | MK |
T7 | 111-113 | http://www.uniprot.org/uniprot/Q03426 | denotes | MK |
T8 | 457-459 | http://www.uniprot.org/uniprot/Q03426 | denotes | MK |
T9 | 1073-1075 | http://www.uniprot.org/uniprot/Q03426 | denotes | MK |
T10 | 1590-1592 | http://www.uniprot.org/uniprot/Q03426 | denotes | MK |
T11 | 718-732 | http://www.uniprot.org/uniprot/P34059 | denotes | chondroitinase |
T12 | 887-889 | http://www.uniprot.org/uniprot/O75390 | denotes | CS |
T13 | 919-942 | http://www.uniprot.org/uniprot/P15848 | denotes | N-acetylgalactosamine 4 |
uniprot-mouse
Id | Subject | Object | Predicate | Lexical cue |
---|---|---|---|---|
T1 | 60-67 | http://www.uniprot.org/uniprot/P12025 | denotes | midkine |
T2 | 102-109 | http://www.uniprot.org/uniprot/P12025 | denotes | Midkine |
T3 | 111-113 | http://www.uniprot.org/uniprot/P12025 | denotes | MK |
T4 | 457-459 | http://www.uniprot.org/uniprot/P12025 | denotes | MK |
T5 | 1073-1075 | http://www.uniprot.org/uniprot/P12025 | denotes | MK |
T6 | 1590-1592 | http://www.uniprot.org/uniprot/P12025 | denotes | MK |
T7 | 111-113 | http://www.uniprot.org/uniprot/Q9R008 | denotes | MK |
T8 | 457-459 | http://www.uniprot.org/uniprot/Q9R008 | denotes | MK |
T9 | 1073-1075 | http://www.uniprot.org/uniprot/Q9R008 | denotes | MK |
T10 | 1590-1592 | http://www.uniprot.org/uniprot/Q9R008 | denotes | MK |
T11 | 111-113 | http://www.uniprot.org/uniprot/Q9QZM4 | denotes | MK |
T12 | 457-459 | http://www.uniprot.org/uniprot/Q9QZM4 | denotes | MK |
T13 | 1073-1075 | http://www.uniprot.org/uniprot/Q9QZM4 | denotes | MK |
T14 | 1590-1592 | http://www.uniprot.org/uniprot/Q9QZM4 | denotes | MK |
T15 | 718-732 | http://www.uniprot.org/uniprot/Q571E4 | denotes | chondroitinase |
GlycoBiology-NCBITAXON
Id | Subject | Object | Predicate | Lexical cue |
---|---|---|---|---|
T1 | 348-351 | http://purl.bioontology.org/ontology/NCBITAXON/82391 | denotes | day |
GO-BP
Id | Subject | Object | Predicate | Lexical cue |
---|---|---|---|---|
T1 | 87-93 | http://purl.obolibrary.org/obo/GO_0040007 | denotes | growth |
T2 | 134-140 | http://purl.obolibrary.org/obo/GO_0040007 | denotes | growth |
T3 | 206-214 | http://purl.obolibrary.org/obo/GO_0051923 | denotes | sulfates |
T4 | 233-240 | http://purl.obolibrary.org/obo/GO_0051923 | denotes | sulfate |
T5 | 943-950 | http://purl.obolibrary.org/obo/GO_0051923 | denotes | sulfate |
T6 | 1110-1119 | http://purl.obolibrary.org/obo/GO_0051923 | denotes | sulfation |
T7 | 1235-1243 | http://purl.obolibrary.org/obo/GO_0051923 | denotes | sulfated |
T8 | 718-732 | http://purl.obolibrary.org/obo/GO_0043890 | denotes | chondroitinase |
T9 | 1283-1292 | http://purl.obolibrary.org/obo/GO_0007586 | denotes | digestion |
GO-MF
Id | Subject | Object | Predicate | Lexical cue |
---|---|---|---|---|
T1 | 49-56 | http://purl.obolibrary.org/obo/GO_0070026 | denotes | binding |
T2 | 79-86 | http://purl.obolibrary.org/obo/GO_0070026 | denotes | binding |
T3 | 126-133 | http://purl.obolibrary.org/obo/GO_0070026 | denotes | binding |
T4 | 314-321 | http://purl.obolibrary.org/obo/GO_0070026 | denotes | binding |
T5 | 504-511 | http://purl.obolibrary.org/obo/GO_0070026 | denotes | binding |
T6 | 569-576 | http://purl.obolibrary.org/obo/GO_0070026 | denotes | binding |
T7 | 698-705 | http://purl.obolibrary.org/obo/GO_0070026 | denotes | binding |
T8 | 858-865 | http://purl.obolibrary.org/obo/GO_0070026 | denotes | binding |
T9 | 1165-1172 | http://purl.obolibrary.org/obo/GO_0070026 | denotes | binding |
T10 | 1369-1376 | http://purl.obolibrary.org/obo/GO_0070026 | denotes | binding |
T11 | 1414-1421 | http://purl.obolibrary.org/obo/GO_0070026 | denotes | binding |
T12 | 149-154 | http://purl.obolibrary.org/obo/GO_0070026 | denotes | binds |
T13 | 49-56 | http://purl.obolibrary.org/obo/GO_0003680 | denotes | binding |
T14 | 79-86 | http://purl.obolibrary.org/obo/GO_0003680 | denotes | binding |
T15 | 126-133 | http://purl.obolibrary.org/obo/GO_0003680 | denotes | binding |
T16 | 314-321 | http://purl.obolibrary.org/obo/GO_0003680 | denotes | binding |
T17 | 504-511 | http://purl.obolibrary.org/obo/GO_0003680 | denotes | binding |
T18 | 569-576 | http://purl.obolibrary.org/obo/GO_0003680 | denotes | binding |
T19 | 698-705 | http://purl.obolibrary.org/obo/GO_0003680 | denotes | binding |
T20 | 858-865 | http://purl.obolibrary.org/obo/GO_0003680 | denotes | binding |
T21 | 1165-1172 | http://purl.obolibrary.org/obo/GO_0003680 | denotes | binding |
T22 | 1369-1376 | http://purl.obolibrary.org/obo/GO_0003680 | denotes | binding |
T23 | 1414-1421 | http://purl.obolibrary.org/obo/GO_0003680 | denotes | binding |
T24 | 149-154 | http://purl.obolibrary.org/obo/GO_0003680 | denotes | binds |
T25 | 49-56 | http://purl.obolibrary.org/obo/GO_0017091 | denotes | binding |
T26 | 79-86 | http://purl.obolibrary.org/obo/GO_0017091 | denotes | binding |
T27 | 126-133 | http://purl.obolibrary.org/obo/GO_0017091 | denotes | binding |
T28 | 314-321 | http://purl.obolibrary.org/obo/GO_0017091 | denotes | binding |
T29 | 504-511 | http://purl.obolibrary.org/obo/GO_0017091 | denotes | binding |
T30 | 569-576 | http://purl.obolibrary.org/obo/GO_0017091 | denotes | binding |
T31 | 698-705 | http://purl.obolibrary.org/obo/GO_0017091 | denotes | binding |
T32 | 858-865 | http://purl.obolibrary.org/obo/GO_0017091 | denotes | binding |
T33 | 1165-1172 | http://purl.obolibrary.org/obo/GO_0017091 | denotes | binding |
T34 | 1369-1376 | http://purl.obolibrary.org/obo/GO_0017091 | denotes | binding |
T35 | 1414-1421 | http://purl.obolibrary.org/obo/GO_0017091 | denotes | binding |
T36 | 149-154 | http://purl.obolibrary.org/obo/GO_0017091 | denotes | binds |
T37 | 49-56 | http://purl.obolibrary.org/obo/GO_0005488 | denotes | binding |
T38 | 79-86 | http://purl.obolibrary.org/obo/GO_0005488 | denotes | binding |
T39 | 126-133 | http://purl.obolibrary.org/obo/GO_0005488 | denotes | binding |
T40 | 314-321 | http://purl.obolibrary.org/obo/GO_0005488 | denotes | binding |
T41 | 504-511 | http://purl.obolibrary.org/obo/GO_0005488 | denotes | binding |
T42 | 569-576 | http://purl.obolibrary.org/obo/GO_0005488 | denotes | binding |
T43 | 698-705 | http://purl.obolibrary.org/obo/GO_0005488 | denotes | binding |
T44 | 858-865 | http://purl.obolibrary.org/obo/GO_0005488 | denotes | binding |
T45 | 1165-1172 | http://purl.obolibrary.org/obo/GO_0005488 | denotes | binding |
T46 | 1369-1376 | http://purl.obolibrary.org/obo/GO_0005488 | denotes | binding |
T47 | 1414-1421 | http://purl.obolibrary.org/obo/GO_0005488 | denotes | binding |
T48 | 149-154 | http://purl.obolibrary.org/obo/GO_0005488 | denotes | binds |
T49 | 71-86 | http://purl.obolibrary.org/obo/GO_0008201 | denotes | heparin-binding |
T50 | 118-133 | http://purl.obolibrary.org/obo/GO_0008201 | denotes | heparin-binding |
T51 | 79-100 | http://purl.obolibrary.org/obo/GO_0019838 | denotes | binding growth factor |
T52 | 134-154 | http://purl.obolibrary.org/obo/GO_0019838 | denotes | growth factor, binds |
T53 | 79-100 | http://purl.obolibrary.org/obo/GO_0048408 | denotes | binding growth factor |
T54 | 134-154 | http://purl.obolibrary.org/obo/GO_0048408 | denotes | growth factor, binds |
T55 | 79-100 | http://purl.obolibrary.org/obo/GO_0036458 | denotes | binding growth factor |
T56 | 134-154 | http://purl.obolibrary.org/obo/GO_0036458 | denotes | growth factor, binds |
T57 | 79-100 | http://purl.obolibrary.org/obo/GO_0017134 | denotes | binding growth factor |
T58 | 134-154 | http://purl.obolibrary.org/obo/GO_0017134 | denotes | growth factor, binds |
T59 | 79-100 | http://purl.obolibrary.org/obo/GO_0048406 | denotes | binding growth factor |
T60 | 134-154 | http://purl.obolibrary.org/obo/GO_0048406 | denotes | growth factor, binds |
T61 | 79-100 | http://purl.obolibrary.org/obo/GO_0070851 | denotes | binding growth factor |
T62 | 134-154 | http://purl.obolibrary.org/obo/GO_0070851 | denotes | growth factor, binds |
UBERON-AE
Id | Subject | Object | Predicate | Lexical cue |
---|---|---|---|---|
T1 | 333-339 | http://purl.obolibrary.org/obo/UBERON_0000955 | denotes | brains |
T2 | 358-365 | http://purl.obolibrary.org/obo/UBERON_0000922 | denotes | embryos |
EDAM-topics
Id | Subject | Object | Predicate | Lexical cue |
---|---|---|---|---|
T1 | 259-271 | http://edamontology.org/topic_0152 | denotes | carbohydrate |
T2 | 1007-1012 | http://edamontology.org/topic_2815 | denotes | human |
T3 | 1056-1067 | http://edamontology.org/topic_0602 | denotes | interaction |
T4 | 1466-1473 | http://edamontology.org/topic_3678 | denotes | studies |
EDAM-DFO
Id | Subject | Object | Predicate | Lexical cue |
---|---|---|---|---|
T1 | 18-28 | http://edamontology.org/data_0883 | denotes | structures |
T2 | 180-190 | http://edamontology.org/data_0883 | denotes | structures |
T3 | 180-193 | http://edamontology.org/data_1070 | denotes | structures in |
T4 | 259-281 | http://edamontology.org/data_1462 | denotes | carbohydrate structure |
T5 | 272-281 | http://edamontology.org/data_0883 | denotes | structure |
T6 | 619-633 | http://edamontology.org/data_2140 | denotes | concentrations |
T7 | 892-901 | http://edamontology.org/data_0883 | denotes | structure |
T8 | 1021-1029 | http://edamontology.org/operation_2945 | denotes | Analysis |
T9 | 1216-1223 | http://edamontology.org/operation_3432 | denotes | cluster |
T10 | 1550-1559 | http://edamontology.org/data_0883 | denotes | structure |
GlycoBiology-MAT
Id | Subject | Object | Predicate | Lexical cue |
---|---|---|---|---|
T1 | 333-339 | http://purl.obolibrary.org/obo/MAT_0000098 | denotes | brains |
T2 | 358-365 | http://purl.obolibrary.org/obo/MAT_0000226 | denotes | embryos |
GlycoBiology-Motifs
Id | Subject | Object | Predicate | Lexical cue |
---|---|---|---|---|
T1 | 71-78 | http://rdf.glycoinfo.org/glycan/G54161DR | denotes | heparin |
T2 | 118-125 | http://rdf.glycoinfo.org/glycan/G54161DR | denotes | heparin |
T3 | 1521-1528 | http://rdf.glycoinfo.org/glycan/G54161DR | denotes | heparin |
T4 | 194-205 | http://rdf.glycoinfo.org/glycan/G00018MO | denotes | chondroitin |
T5 | 194-214 | http://rdf.glycoinfo.org/glycan/G00018MO | denotes | chondroitin sulfates |
GlycoBiology-Epitope
Id | Subject | Object | Predicate | Lexical cue |
---|---|---|---|---|
PD-GlycoEpitope-B_T1 | 409-416 | id | denotes | labeled |
PD-GlycoEpitope-B_T2 | 194-205 | http://www.glycoepitope.jp/epitopes/EP0081 | denotes | chondroitin |
PD-GlycoEpitope-B_T3 | 225-240 | http://www.glycoepitope.jp/epitopes/EP0086 | denotes | heparan sulfate |
performance-test
Id | Subject | Object | Predicate | Lexical cue |
---|---|---|---|---|
PD-UBERON-AE-B_T1 | 333-339 | http://purl.obolibrary.org/obo/UBERON_0000955 | denotes | brains |
PD-UBERON-AE-B_T2 | 358-365 | http://purl.obolibrary.org/obo/UBERON_0000922 | denotes | embryos |
Anatomy-MAT
Id | Subject | Object | Predicate | Lexical cue | mat_id |
---|---|---|---|---|---|
T1 | 333-339 | Body_part | denotes | brains | http://purl.obolibrary.org/obo/MAT_0000098 |
T2 | 358-365 | Body_part | denotes | embryos | http://purl.obolibrary.org/obo/MAT_0000226 |
Glycan-GlyCosmos
Id | Subject | Object | Predicate | Lexical cue | image |
---|---|---|---|---|---|
T1 | 194-205 | Glycan | denotes | chondroitin | https://api.glycosmos.org/wurcs2image/latest/png/binary/G43702JT |
T2 | 225-240 | Glycan | denotes | heparan sulfate | https://api.glycosmos.org/wurcs2image/latest/png/binary/G17927IW |
GlyCosmos-GlycoEpitope
Id | Subject | Object | Predicate | Lexical cue | glycoepitope_id |
---|---|---|---|---|---|
T1 | 194-205 | http://purl.jp/bio/12/glyco/glycan#Glycan_epitope | denotes | chondroitin | http://www.glycoepitope.jp/epitopes/EP0081 |
T2 | 225-240 | http://purl.jp/bio/12/glyco/glycan#Glycan_epitope | denotes | heparan sulfate | http://www.glycoepitope.jp/epitopes/EP0086 |
GlyCosmos15-NCBITAXON
Id | Subject | Object | Predicate | Lexical cue | db_id |
---|---|---|---|---|---|
T1 | 352-357 | OrganismTaxon | denotes | mouse | 10088|10090 |
T3 | 1007-1012 | OrganismTaxon | denotes | human | 9606 |
GlyCosmos15-MAT
Id | Subject | Object | Predicate | Lexical cue | mat_id |
---|---|---|---|---|---|
T1 | 333-339 | Body_part | denotes | brains | http://purl.obolibrary.org/obo/MAT_0000098 |
T2 | 358-365 | Body_part | denotes | embryos | http://purl.obolibrary.org/obo/MAT_0000226 |
sentences
Id | Subject | Object | Predicate | Lexical cue |
---|---|---|---|---|
TextSentencer_T1 | 0-101 | Sentence | denotes | Glycosaminoglycan structures required for strong binding to midkine, a heparin-binding growth factor. |
TextSentencer_T2 | 102-241 | Sentence | denotes | Midkine (MK), a heparin-binding growth factor, binds strongly to oversulfated structures in chondroitin sulfates (CSs) and heparan sulfate. |
TextSentencer_T3 | 242-404 | Sentence | denotes | To elucidate the carbohydrate structure actually involved in the strong binding, dissected brains from 13-day mouse embryos were incubated with [14C]-glucosamine. |
TextSentencer_T4 | 405-634 | Sentence | denotes | The labeled glycosaminoglycans were fractionated by MK-agarose affinity chromatography to a weakly binding fraction, which was eluted by 0.5 M NaCl, and a strongly binding fraction, which was eluted by higher NaCl concentrations. |
TextSentencer_T5 | 635-875 | Sentence | denotes | Among the unsaturated disaccharides released from the strongly binding fraction by chondroitinase ABC, DeltaDi-diSE with 4,6-disulfated N-acetylgalactosamine accounted for 32.3%, whereas its content was lower in the weakly binding fraction. |
TextSentencer_T6 | 876-1020 | Sentence | denotes | Artificial CS-E structure was formed using N-acetylgalactosamine 4-sulfate 6-O-sulfotransferase purified from squid or recombinant human enzyme. |
TextSentencer_T7 | 1021-1224 | Sentence | denotes | Analysis of the products and their interaction with MK revealed that E units without 3-O-sulfation of glucuronic acid are sufficient for strong binding, provided that they are present as a dense cluster. |
TextSentencer_T8 | 1225-1431 | Sentence | denotes | Among the sulfated disaccharides released by heparitinase digestion, the trisulfated one, DeltaDiHS-triS, was the most abundant in the strongly binding fraction and was lower in the weakly binding fraction. |
TextSentencer_T9 | 1432-1593 | Sentence | denotes | Together with results of previous studies, we concluded that the multivalent trisulfated heparin-like unit is another structure involved in strong binding to MK. |
T1 | 0-101 | Sentence | denotes | Glycosaminoglycan structures required for strong binding to midkine, a heparin-binding growth factor. |
T2 | 102-241 | Sentence | denotes | Midkine (MK), a heparin-binding growth factor, binds strongly to oversulfated structures in chondroitin sulfates (CSs) and heparan sulfate. |
T3 | 242-404 | Sentence | denotes | To elucidate the carbohydrate structure actually involved in the strong binding, dissected brains from 13-day mouse embryos were incubated with [14C]-glucosamine. |
T4 | 405-634 | Sentence | denotes | The labeled glycosaminoglycans were fractionated by MK-agarose affinity chromatography to a weakly binding fraction, which was eluted by 0.5 M NaCl, and a strongly binding fraction, which was eluted by higher NaCl concentrations. |
T5 | 635-875 | Sentence | denotes | Among the unsaturated disaccharides released from the strongly binding fraction by chondroitinase ABC, DeltaDi-diSE with 4,6-disulfated N-acetylgalactosamine accounted for 32.3%, whereas its content was lower in the weakly binding fraction. |
T6 | 876-1020 | Sentence | denotes | Artificial CS-E structure was formed using N-acetylgalactosamine 4-sulfate 6-O-sulfotransferase purified from squid or recombinant human enzyme. |
T7 | 1021-1224 | Sentence | denotes | Analysis of the products and their interaction with MK revealed that E units without 3-O-sulfation of glucuronic acid are sufficient for strong binding, provided that they are present as a dense cluster. |
T8 | 1225-1431 | Sentence | denotes | Among the sulfated disaccharides released by heparitinase digestion, the trisulfated one, DeltaDiHS-triS, was the most abundant in the strongly binding fraction and was lower in the weakly binding fraction. |
T9 | 1432-1593 | Sentence | denotes | Together with results of previous studies, we concluded that the multivalent trisulfated heparin-like unit is another structure involved in strong binding to MK. |
T1 | 0-101 | Sentence | denotes | Glycosaminoglycan structures required for strong binding to midkine, a heparin-binding growth factor. |
T2 | 102-241 | Sentence | denotes | Midkine (MK), a heparin-binding growth factor, binds strongly to oversulfated structures in chondroitin sulfates (CSs) and heparan sulfate. |
T3 | 242-404 | Sentence | denotes | To elucidate the carbohydrate structure actually involved in the strong binding, dissected brains from 13-day mouse embryos were incubated with [14C]-glucosamine. |
T4 | 405-634 | Sentence | denotes | The labeled glycosaminoglycans were fractionated by MK-agarose affinity chromatography to a weakly binding fraction, which was eluted by 0.5 M NaCl, and a strongly binding fraction, which was eluted by higher NaCl concentrations. |
T5 | 635-875 | Sentence | denotes | Among the unsaturated disaccharides released from the strongly binding fraction by chondroitinase ABC, DeltaDi-diSE with 4,6-disulfated N-acetylgalactosamine accounted for 32.3%, whereas its content was lower in the weakly binding fraction. |
T6 | 876-1020 | Sentence | denotes | Artificial CS-E structure was formed using N-acetylgalactosamine 4-sulfate 6-O-sulfotransferase purified from squid or recombinant human enzyme. |
T7 | 1021-1224 | Sentence | denotes | Analysis of the products and their interaction with MK revealed that E units without 3-O-sulfation of glucuronic acid are sufficient for strong binding, provided that they are present as a dense cluster. |
T8 | 1225-1431 | Sentence | denotes | Among the sulfated disaccharides released by heparitinase digestion, the trisulfated one, DeltaDiHS-triS, was the most abundant in the strongly binding fraction and was lower in the weakly binding fraction. |
T9 | 1432-1593 | Sentence | denotes | Together with results of previous studies, we concluded that the multivalent trisulfated heparin-like unit is another structure involved in strong binding to MK. |
GlyCosmos15-Sentences
Id | Subject | Object | Predicate | Lexical cue |
---|---|---|---|---|
T1 | 0-101 | Sentence | denotes | Glycosaminoglycan structures required for strong binding to midkine, a heparin-binding growth factor. |
T2 | 102-241 | Sentence | denotes | Midkine (MK), a heparin-binding growth factor, binds strongly to oversulfated structures in chondroitin sulfates (CSs) and heparan sulfate. |
T3 | 242-404 | Sentence | denotes | To elucidate the carbohydrate structure actually involved in the strong binding, dissected brains from 13-day mouse embryos were incubated with [14C]-glucosamine. |
T4 | 405-634 | Sentence | denotes | The labeled glycosaminoglycans were fractionated by MK-agarose affinity chromatography to a weakly binding fraction, which was eluted by 0.5 M NaCl, and a strongly binding fraction, which was eluted by higher NaCl concentrations. |
T5 | 635-875 | Sentence | denotes | Among the unsaturated disaccharides released from the strongly binding fraction by chondroitinase ABC, DeltaDi-diSE with 4,6-disulfated N-acetylgalactosamine accounted for 32.3%, whereas its content was lower in the weakly binding fraction. |
T6 | 876-1020 | Sentence | denotes | Artificial CS-E structure was formed using N-acetylgalactosamine 4-sulfate 6-O-sulfotransferase purified from squid or recombinant human enzyme. |
T7 | 1021-1224 | Sentence | denotes | Analysis of the products and their interaction with MK revealed that E units without 3-O-sulfation of glucuronic acid are sufficient for strong binding, provided that they are present as a dense cluster. |
T8 | 1225-1431 | Sentence | denotes | Among the sulfated disaccharides released by heparitinase digestion, the trisulfated one, DeltaDiHS-triS, was the most abundant in the strongly binding fraction and was lower in the weakly binding fraction. |
T9 | 1432-1593 | Sentence | denotes | Together with results of previous studies, we concluded that the multivalent trisulfated heparin-like unit is another structure involved in strong binding to MK. |
GlyCosmos15-Glycan
Id | Subject | Object | Predicate | Lexical cue | image |
---|---|---|---|---|---|
T1 | 194-205 | Glycan | denotes | chondroitin | https://api.glycosmos.org/wurcs2image/latest/png/binary/G43702JT |
T2 | 225-240 | Glycan | denotes | heparan sulfate | https://api.glycosmos.org/wurcs2image/latest/png/binary/G17927IW |
GlyCosmos15-GlycoEpitope
Id | Subject | Object | Predicate | Lexical cue | glycoepitope_id |
---|---|---|---|---|---|
T1 | 194-205 | http://purl.jp/bio/12/glyco/glycan#Glycan_epitope | denotes | chondroitin | http://www.glycoepitope.jp/epitopes/EP0081 |
T2 | 225-240 | http://purl.jp/bio/12/glyco/glycan#Glycan_epitope | denotes | heparan sulfate | http://www.glycoepitope.jp/epitopes/EP0086 |
NCBITAXON
Id | Subject | Object | Predicate | Lexical cue | db_id |
---|---|---|---|---|---|
T1 | 352-357 | OrganismTaxon | denotes | mouse | 10088|10090 |
T3 | 1007-1012 | OrganismTaxon | denotes | human | 9606 |