PubMed:22997241
Annnotations
Glycan-Motif
Id | Subject | Object | Predicate | Lexical cue |
---|---|---|---|---|
T1 | 54-61 | https://glytoucan.org/Structures/Glycans/G00021MO | denotes | heparin |
T2 | 54-61 | https://glytoucan.org/Structures/Glycans/G54161DR | denotes | heparin |
T3 | 767-774 | https://glytoucan.org/Structures/Glycans/G00021MO | denotes | heparin |
T4 | 767-774 | https://glytoucan.org/Structures/Glycans/G54161DR | denotes | heparin |
T5 | 843-850 | https://glytoucan.org/Structures/Glycans/G00021MO | denotes | heparin |
T6 | 843-850 | https://glytoucan.org/Structures/Glycans/G54161DR | denotes | heparin |
T7 | 1182-1189 | https://glytoucan.org/Structures/Glycans/G00021MO | denotes | heparin |
T8 | 1182-1189 | https://glytoucan.org/Structures/Glycans/G54161DR | denotes | heparin |
T9 | 1276-1283 | https://glytoucan.org/Structures/Glycans/G00021MO | denotes | heparin |
T10 | 1276-1283 | https://glytoucan.org/Structures/Glycans/G54161DR | denotes | heparin |
T11 | 1288-1295 | https://glytoucan.org/Structures/Glycans/G00021MO | denotes | heparin |
T12 | 1288-1295 | https://glytoucan.org/Structures/Glycans/G54161DR | denotes | heparin |
T13 | 1349-1356 | https://glytoucan.org/Structures/Glycans/G00021MO | denotes | heparin |
T14 | 1349-1356 | https://glytoucan.org/Structures/Glycans/G54161DR | denotes | heparin |
PubMed_ArguminSci
Id | Subject | Object | Predicate | Lexical cue |
---|---|---|---|---|
T1 | 74-262 | DRI_Challenge | denotes | Toxoplasma gondii is the causative agent of toxoplasmosis, one of the most widespread infections in humans and animals, and is a major opportunistic pathogen in immunocompromised patients. |
T2 | 263-392 | DRI_Outcome | denotes | Toxoplasma gondii is unique as it can invade virtually any nucleated cell, although the mechanisms are not completely understood. |
T3 | 393-556 | DRI_Challenge | denotes | Parasite attachment to the host cell is a prerequisite for reorientation and penetration and likely requires the recognition of molecules at the host cell surface. |
T4 | 557-760 | DRI_Outcome | denotes | It has been reported that the affinity of tachyzoites, the invasive form of T. gondii, for host cells can be inhibited by a variety of soluble-sulfated glycosaminoglycans (GAGs), such as heparan sulfate. |
T5 | 761-935 | DRI_Approach | denotes | Using heparin-functionalized zeolites in the absence of host cells, we visualized heparin-binding sites on the surface of tachyzoites by confocal and atomic force microscopy. |
T6 | 936-1044 | DRI_Outcome | denotes | Furthermore, we report that protein components of the parasite rhoptry, dense granule and surface bind GAGs. |
T7 | 1045-1190 | DRI_Background | denotes | In particular, the proteins ROP2 and ROP4 from the rhoptry, GRA2 from the dense granules and the surface protein SAG1 were found to bind heparin. |
T8 | 1191-1415 | DRI_Outcome | denotes | The binding specificities and affinities of individual parasite proteins for natural heparin and heparin oligosaccharides were determined by a combination of heparin oligosaccharide microarrays and surface plasmon resonance. |
T9 | 1416-1792 | DRI_Outcome | denotes | Our results suggest that interactions between sulfated GAGs and parasite surface antigens contribute to T. gondii attachment to host cell surfaces as well as initiating the invasion process, while rhoptries and dense granule organelles may play an important role during the establishment of the infection and during the life of the parasite inside the parasitophorous vacuole. |
GlyCosmos6-Glycan-Motif-Image
Id | Subject | Object | Predicate | Lexical cue | image |
---|---|---|---|---|---|
T1 | 54-61 | 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 | 767-774 | 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 | 843-850 | 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 |
T7 | 1182-1189 | 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 |
T9 | 1276-1283 | 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 |
T11 | 1288-1295 | 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 |
T13 | 1349-1356 | 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 | 0-73 | Sentence | denotes | Toxoplasma gondii secretory proteins bind to sulfated heparin structures. |
TextSentencer_T2 | 74-262 | Sentence | denotes | Toxoplasma gondii is the causative agent of toxoplasmosis, one of the most widespread infections in humans and animals, and is a major opportunistic pathogen in immunocompromised patients. |
TextSentencer_T3 | 263-392 | Sentence | denotes | Toxoplasma gondii is unique as it can invade virtually any nucleated cell, although the mechanisms are not completely understood. |
TextSentencer_T4 | 393-556 | Sentence | denotes | Parasite attachment to the host cell is a prerequisite for reorientation and penetration and likely requires the recognition of molecules at the host cell surface. |
TextSentencer_T5 | 557-760 | Sentence | denotes | It has been reported that the affinity of tachyzoites, the invasive form of T. gondii, for host cells can be inhibited by a variety of soluble-sulfated glycosaminoglycans (GAGs), such as heparan sulfate. |
TextSentencer_T6 | 761-935 | Sentence | denotes | Using heparin-functionalized zeolites in the absence of host cells, we visualized heparin-binding sites on the surface of tachyzoites by confocal and atomic force microscopy. |
TextSentencer_T7 | 936-1044 | Sentence | denotes | Furthermore, we report that protein components of the parasite rhoptry, dense granule and surface bind GAGs. |
TextSentencer_T8 | 1045-1190 | Sentence | denotes | In particular, the proteins ROP2 and ROP4 from the rhoptry, GRA2 from the dense granules and the surface protein SAG1 were found to bind heparin. |
TextSentencer_T9 | 1191-1415 | Sentence | denotes | The binding specificities and affinities of individual parasite proteins for natural heparin and heparin oligosaccharides were determined by a combination of heparin oligosaccharide microarrays and surface plasmon resonance. |
TextSentencer_T10 | 1416-1792 | Sentence | denotes | Our results suggest that interactions between sulfated GAGs and parasite surface antigens contribute to T. gondii attachment to host cell surfaces as well as initiating the invasion process, while rhoptries and dense granule organelles may play an important role during the establishment of the infection and during the life of the parasite inside the parasitophorous vacuole. |
T1 | 0-73 | Sentence | denotes | Toxoplasma gondii secretory proteins bind to sulfated heparin structures. |
T2 | 74-262 | Sentence | denotes | Toxoplasma gondii is the causative agent of toxoplasmosis, one of the most widespread infections in humans and animals, and is a major opportunistic pathogen in immunocompromised patients. |
T3 | 263-392 | Sentence | denotes | Toxoplasma gondii is unique as it can invade virtually any nucleated cell, although the mechanisms are not completely understood. |
T4 | 393-556 | Sentence | denotes | Parasite attachment to the host cell is a prerequisite for reorientation and penetration and likely requires the recognition of molecules at the host cell surface. |
T5 | 557-760 | Sentence | denotes | It has been reported that the affinity of tachyzoites, the invasive form of T. gondii, for host cells can be inhibited by a variety of soluble-sulfated glycosaminoglycans (GAGs), such as heparan sulfate. |
T6 | 761-935 | Sentence | denotes | Using heparin-functionalized zeolites in the absence of host cells, we visualized heparin-binding sites on the surface of tachyzoites by confocal and atomic force microscopy. |
T7 | 936-1044 | Sentence | denotes | Furthermore, we report that protein components of the parasite rhoptry, dense granule and surface bind GAGs. |
T8 | 1045-1190 | Sentence | denotes | In particular, the proteins ROP2 and ROP4 from the rhoptry, GRA2 from the dense granules and the surface protein SAG1 were found to bind heparin. |
T9 | 1191-1415 | Sentence | denotes | The binding specificities and affinities of individual parasite proteins for natural heparin and heparin oligosaccharides were determined by a combination of heparin oligosaccharide microarrays and surface plasmon resonance. |
T10 | 1416-1792 | Sentence | denotes | Our results suggest that interactions between sulfated GAGs and parasite surface antigens contribute to T. gondii attachment to host cell surfaces as well as initiating the invasion process, while rhoptries and dense granule organelles may play an important role during the establishment of the infection and during the life of the parasite inside the parasitophorous vacuole. |
T1 | 0-73 | Sentence | denotes | Toxoplasma gondii secretory proteins bind to sulfated heparin structures. |
T2 | 74-262 | Sentence | denotes | Toxoplasma gondii is the causative agent of toxoplasmosis, one of the most widespread infections in humans and animals, and is a major opportunistic pathogen in immunocompromised patients. |
T3 | 263-392 | Sentence | denotes | Toxoplasma gondii is unique as it can invade virtually any nucleated cell, although the mechanisms are not completely understood. |
T4 | 393-556 | Sentence | denotes | Parasite attachment to the host cell is a prerequisite for reorientation and penetration and likely requires the recognition of molecules at the host cell surface. |
T5 | 557-760 | Sentence | denotes | It has been reported that the affinity of tachyzoites, the invasive form of T. gondii, for host cells can be inhibited by a variety of soluble-sulfated glycosaminoglycans (GAGs), such as heparan sulfate. |
T6 | 761-935 | Sentence | denotes | Using heparin-functionalized zeolites in the absence of host cells, we visualized heparin-binding sites on the surface of tachyzoites by confocal and atomic force microscopy. |
T7 | 936-1044 | Sentence | denotes | Furthermore, we report that protein components of the parasite rhoptry, dense granule and surface bind GAGs. |
T8 | 1045-1190 | Sentence | denotes | In particular, the proteins ROP2 and ROP4 from the rhoptry, GRA2 from the dense granules and the surface protein SAG1 were found to bind heparin. |
T9 | 1191-1415 | Sentence | denotes | The binding specificities and affinities of individual parasite proteins for natural heparin and heparin oligosaccharides were determined by a combination of heparin oligosaccharide microarrays and surface plasmon resonance. |
T10 | 1416-1792 | Sentence | denotes | Our results suggest that interactions between sulfated GAGs and parasite surface antigens contribute to T. gondii attachment to host cell surfaces as well as initiating the invasion process, while rhoptries and dense granule organelles may play an important role during the establishment of the infection and during the life of the parasite inside the parasitophorous vacuole. |
GlyCosmos6-Glycan-Motif-Structure
Id | Subject | Object | Predicate | Lexical cue |
---|---|---|---|---|
T1 | 54-61 | https://glytoucan.org/Structures/Glycans/G00021MO | denotes | heparin |
T2 | 54-61 | https://glytoucan.org/Structures/Glycans/G54161DR | denotes | heparin |
T3 | 767-774 | https://glytoucan.org/Structures/Glycans/G00021MO | denotes | heparin |
T4 | 767-774 | https://glytoucan.org/Structures/Glycans/G54161DR | denotes | heparin |
T5 | 843-850 | https://glytoucan.org/Structures/Glycans/G00021MO | denotes | heparin |
T6 | 843-850 | https://glytoucan.org/Structures/Glycans/G54161DR | denotes | heparin |
T7 | 1182-1189 | https://glytoucan.org/Structures/Glycans/G00021MO | denotes | heparin |
T8 | 1182-1189 | https://glytoucan.org/Structures/Glycans/G54161DR | denotes | heparin |
T9 | 1276-1283 | https://glytoucan.org/Structures/Glycans/G00021MO | denotes | heparin |
T10 | 1276-1283 | https://glytoucan.org/Structures/Glycans/G54161DR | denotes | heparin |
T11 | 1288-1295 | https://glytoucan.org/Structures/Glycans/G00021MO | denotes | heparin |
T12 | 1288-1295 | https://glytoucan.org/Structures/Glycans/G54161DR | denotes | heparin |
T13 | 1349-1356 | https://glytoucan.org/Structures/Glycans/G00021MO | denotes | heparin |
T14 | 1349-1356 | https://glytoucan.org/Structures/Glycans/G54161DR | denotes | heparin |
Glycosmos6-GlycoEpitope
Id | Subject | Object | Predicate | Lexical cue |
---|---|---|---|---|
T1 | 744-759 | http://www.glycoepitope.jp/epitopes/EP0086 | denotes | heparan sulfate |
PubmedHPO
Id | Subject | Object | Predicate | Lexical cue |
---|---|---|---|---|
T1 | 1008-1013 | HP_0011088 | denotes | dense |
T2 | 1119-1124 | HP_0011088 | denotes | dense |
T3 | 1627-1632 | HP_0011088 | denotes | dense |
ICD10
Id | Subject | Object | Predicate | Lexical cue |
---|---|---|---|---|
T1 | 118-131 | http://purl.bioontology.org/ontology/ICD10/B58.9 | denotes | toxoplasmosis |
T2 | 118-131 | http://purl.bioontology.org/ontology/ICD10/B58 | denotes | toxoplasmosis |
GlycoBiology-FMA
Id | Subject | Object | Predicate | Lexical cue |
---|---|---|---|---|
_T1 | 28-36 | FMAID:165447 | denotes | proteins |
_T2 | 28-36 | FMAID:67257 | denotes | proteins |
_T3 | 54-61 | FMAID:82839 | denotes | heparin |
_T4 | 54-61 | FMAID:167420 | denotes | heparin |
_T5 | 318-336 | FMAID:169004 | denotes | any nucleated cell |
_T6 | 322-336 | FMAID:68647 | denotes | nucleated cell |
_T7 | 322-336 | FMAID:169003 | denotes | nucleated cell |
_T8 | 322-336 | FMAID:67513 | denotes | nucleated cell |
_T9 | 322-336 | FMAID:166084 | denotes | nucleated cell |
_T10 | 543-555 | FMAID:212684 | denotes | cell surface |
_T11 | 543-555 | FMAID:200942 | denotes | cell surface |
_T12 | 548-555 | FMAID:146300 | denotes | surface |
_T13 | 548-555 | FMAID:50594 | denotes | surface |
_T14 | 653-658 | FMAID:68646 | denotes | cells |
_T15 | 653-658 | FMAID:169002 | denotes | cells |
_T16 | 709-727 | FMAID:63011 | denotes | glycosaminoglycans |
_T17 | 709-727 | FMAID:167395 | denotes | glycosaminoglycans |
_T18 | 729-733 | FMAID:167404 | denotes | GAGs |
_T19 | 744-751 | FMAID:67110 | denotes | heparan |
_T20 | 744-751 | FMAID:165191 | denotes | heparan |
_T21 | 744-759 | FMAID:63023 | denotes | heparan sulfate |
_T22 | 744-759 | FMAID:167405 | denotes | heparan sulfate |
_T23 | 767-774 | FMAID:82839 | denotes | heparin |
_T24 | 767-774 | FMAID:167420 | denotes | heparin |
_T25 | 822-827 | FMAID:169002 | denotes | cells |
_T26 | 822-827 | FMAID:68646 | denotes | cells |
_T27 | 843-850 | FMAID:82839 | denotes | heparin |
_T28 | 843-850 | FMAID:167420 | denotes | heparin |
_T29 | 872-879 | FMAID:50594 | denotes | surface |
_T30 | 872-879 | FMAID:146300 | denotes | surface |
_T31 | 964-971 | FMAID:165447 | denotes | protein |
_T32 | 964-971 | FMAID:67257 | denotes | protein |
_T33 | 964-982 | FMAID:210763 | denotes | protein components |
_T34 | 1022-1033 | FMAID:212744 | denotes | and surface |
_T35 | 1026-1033 | FMAID:146300 | denotes | surface |
_T36 | 1026-1033 | FMAID:50594 | denotes | surface |
_T37 | 1039-1043 | FMAID:167404 | denotes | GAGs |
_T38 | 1064-1072 | FMAID:165447 | denotes | proteins |
_T39 | 1064-1072 | FMAID:67257 | denotes | proteins |
_T40 | 1142-1149 | FMAID:146300 | denotes | surface |
_T41 | 1142-1149 | FMAID:50594 | denotes | surface |
_T42 | 1150-1157 | FMAID:165447 | denotes | protein |
_T43 | 1150-1157 | FMAID:67257 | denotes | protein |
_T44 | 1182-1189 | FMAID:82839 | denotes | heparin |
_T45 | 1182-1189 | FMAID:167420 | denotes | heparin |
_T46 | 1255-1263 | FMAID:67257 | denotes | proteins |
_T47 | 1255-1263 | FMAID:165447 | denotes | proteins |
_T48 | 1276-1283 | FMAID:167420 | denotes | heparin |
_T49 | 1276-1283 | FMAID:82839 | denotes | heparin |
_T50 | 1288-1295 | FMAID:82839 | denotes | heparin |
_T51 | 1288-1295 | FMAID:167420 | denotes | heparin |
_T52 | 1296-1312 | FMAID:196731 | denotes | oligosaccharides |
_T53 | 1296-1312 | FMAID:82742 | denotes | oligosaccharides |
_T54 | 1349-1356 | FMAID:82839 | denotes | heparin |
_T55 | 1349-1356 | FMAID:167420 | denotes | heparin |
_T56 | 1357-1372 | FMAID:196731 | denotes | oligosaccharide |
_T57 | 1357-1372 | FMAID:82742 | denotes | oligosaccharide |
_T58 | 1385-1396 | FMAID:212744 | denotes | and surface |
_T59 | 1389-1396 | FMAID:50594 | denotes | surface |
_T60 | 1389-1396 | FMAID:146300 | denotes | surface |
_T61 | 1471-1475 | FMAID:167404 | denotes | GAGs |
_T62 | 1489-1496 | FMAID:146300 | denotes | surface |
_T63 | 1489-1496 | FMAID:50594 | denotes | surface |
_T64 | 1549-1562 | FMAID:212684 | denotes | cell surfaces |
_T65 | 1549-1562 | FMAID:200942 | denotes | cell surfaces |
_T66 | 1554-1562 | FMAID:50594 | denotes | surfaces |
_T67 | 1554-1562 | FMAID:146300 | denotes | surfaces |
_T68 | 1641-1651 | FMAID:162296 | denotes | organelles |
_T69 | 1641-1651 | FMAID:63832 | denotes | organelles |
_T70 | 1641-1651 | FMAID:226763 | denotes | organelles |
GlycoBiology-NCBITAXON
Id | Subject | Object | Predicate | Lexical cue |
---|---|---|---|---|
T1 | 0-10 | http://purl.bioontology.org/ontology/NCBITAXON/241603 | denotes | Toxoplasma |
T2 | 0-10 | http://purl.bioontology.org/ontology/NCBITAXON/5810 | denotes | Toxoplasma |
T3 | 0-10 | http://purl.bioontology.org/ontology/NCBITAXON/152250 | denotes | Toxoplasma |
T4 | 0-17 | http://purl.bioontology.org/ontology/NCBITAXON/5811 | denotes | Toxoplasma gondii |
T5 | 74-84 | http://purl.bioontology.org/ontology/NCBITAXON/152250 | denotes | Toxoplasma |
T6 | 74-84 | http://purl.bioontology.org/ontology/NCBITAXON/241603 | denotes | Toxoplasma |
T7 | 74-84 | http://purl.bioontology.org/ontology/NCBITAXON/5810 | denotes | Toxoplasma |
T8 | 74-91 | http://purl.bioontology.org/ontology/NCBITAXON/5811 | denotes | Toxoplasma gondii |
T9 | 263-273 | http://purl.bioontology.org/ontology/NCBITAXON/152250 | denotes | Toxoplasma |
T10 | 263-273 | http://purl.bioontology.org/ontology/NCBITAXON/241603 | denotes | Toxoplasma |
T11 | 263-273 | http://purl.bioontology.org/ontology/NCBITAXON/5810 | denotes | Toxoplasma |
T12 | 263-280 | http://purl.bioontology.org/ontology/NCBITAXON/5811 | denotes | Toxoplasma gondii |
T13 | 351-361 | http://purl.bioontology.org/ontology/NCBITAXON/127244 | denotes | mechanisms |
T14 | 393-401 | http://purl.bioontology.org/ontology/NCBITAXON/600794 | denotes | Parasite |
T15 | 653-658 | http://purl.bioontology.org/ontology/STY/T025 | denotes | cells |
T16 | 822-827 | http://purl.bioontology.org/ontology/STY/T025 | denotes | cells |
T17 | 990-998 | http://purl.bioontology.org/ontology/NCBITAXON/600794 | denotes | parasite |
T18 | 1246-1254 | http://purl.bioontology.org/ontology/NCBITAXON/600794 | denotes | parasite |
T19 | 1480-1488 | http://purl.bioontology.org/ontology/NCBITAXON/600794 | denotes | parasite |
T20 | 1748-1756 | http://purl.bioontology.org/ontology/NCBITAXON/600794 | denotes | parasite |
GO-BP
Id | Subject | Object | Predicate | Lexical cue |
---|---|---|---|---|
T1 | 45-53 | http://purl.obolibrary.org/obo/GO_0051923 | denotes | sulfated |
T2 | 700-708 | http://purl.obolibrary.org/obo/GO_0051923 | denotes | sulfated |
T3 | 752-759 | http://purl.obolibrary.org/obo/GO_0051923 | denotes | sulfate |
T4 | 393-401 | http://purl.obolibrary.org/obo/GO_0072519 | denotes | Parasite |
T5 | 990-998 | http://purl.obolibrary.org/obo/GO_0072519 | denotes | parasite |
T6 | 1246-1254 | http://purl.obolibrary.org/obo/GO_0072519 | denotes | parasite |
T7 | 1480-1488 | http://purl.obolibrary.org/obo/GO_0072519 | denotes | parasite |
T8 | 1748-1756 | http://purl.obolibrary.org/obo/GO_0072519 | denotes | parasite |
GO-MF
Id | Subject | Object | Predicate | Lexical cue |
---|---|---|---|---|
T1 | 28-41 | http://purl.obolibrary.org/obo/GO_0005515 | denotes | proteins bind |
T2 | 37-41 | http://purl.obolibrary.org/obo/GO_0070026 | denotes | bind |
T3 | 1034-1038 | http://purl.obolibrary.org/obo/GO_0070026 | denotes | bind |
T4 | 851-858 | http://purl.obolibrary.org/obo/GO_0070026 | denotes | binding |
T5 | 1195-1202 | http://purl.obolibrary.org/obo/GO_0070026 | denotes | binding |
T6 | 37-41 | http://purl.obolibrary.org/obo/GO_0003680 | denotes | bind |
T7 | 1034-1038 | http://purl.obolibrary.org/obo/GO_0003680 | denotes | bind |
T8 | 851-858 | http://purl.obolibrary.org/obo/GO_0003680 | denotes | binding |
T9 | 1195-1202 | http://purl.obolibrary.org/obo/GO_0003680 | denotes | binding |
T10 | 37-41 | http://purl.obolibrary.org/obo/GO_0017091 | denotes | bind |
T11 | 1034-1038 | http://purl.obolibrary.org/obo/GO_0017091 | denotes | bind |
T12 | 851-858 | http://purl.obolibrary.org/obo/GO_0017091 | denotes | binding |
T13 | 1195-1202 | http://purl.obolibrary.org/obo/GO_0017091 | denotes | binding |
T14 | 37-41 | http://purl.obolibrary.org/obo/GO_0005488 | denotes | bind |
T15 | 1034-1038 | http://purl.obolibrary.org/obo/GO_0005488 | denotes | bind |
T16 | 851-858 | http://purl.obolibrary.org/obo/GO_0005488 | denotes | binding |
T17 | 1195-1202 | http://purl.obolibrary.org/obo/GO_0005488 | denotes | binding |
T18 | 37-53 | http://purl.obolibrary.org/obo/GO_0043199 | denotes | bind to sulfated |
T19 | 538-555 | http://purl.obolibrary.org/obo/GO_0046812 | denotes | host cell surface |
T20 | 1544-1562 | http://purl.obolibrary.org/obo/GO_0046812 | denotes | host cell surfaces |
T21 | 843-858 | http://purl.obolibrary.org/obo/GO_0008201 | denotes | heparin-binding |
T22 | 1182-1202 | http://purl.obolibrary.org/obo/GO_0008201 | denotes | heparin. The binding |
GO-CC
Id | Subject | Object | Predicate | Lexical cue |
---|---|---|---|---|
T1 | 332-336 | http://purl.obolibrary.org/obo/GO_0005623 | denotes | cell |
T2 | 425-429 | http://purl.obolibrary.org/obo/GO_0005623 | denotes | cell |
T3 | 543-547 | http://purl.obolibrary.org/obo/GO_0005623 | denotes | cell |
T4 | 653-658 | http://purl.obolibrary.org/obo/GO_0005623 | denotes | cells |
T5 | 822-827 | http://purl.obolibrary.org/obo/GO_0005623 | denotes | cells |
T6 | 420-424 | http://purl.obolibrary.org/obo/GO_0018995 | denotes | host |
T7 | 538-542 | http://purl.obolibrary.org/obo/GO_0018995 | denotes | host |
T8 | 648-652 | http://purl.obolibrary.org/obo/GO_0018995 | denotes | host |
T9 | 817-821 | http://purl.obolibrary.org/obo/GO_0018995 | denotes | host |
T10 | 1544-1548 | http://purl.obolibrary.org/obo/GO_0018995 | denotes | host |
T11 | 420-429 | http://purl.obolibrary.org/obo/GO_0043657 | denotes | host cell |
T12 | 538-547 | http://purl.obolibrary.org/obo/GO_0043657 | denotes | host cell |
T13 | 648-658 | http://purl.obolibrary.org/obo/GO_0043657 | denotes | host cells |
T14 | 817-827 | http://purl.obolibrary.org/obo/GO_0043657 | denotes | host cells |
T15 | 538-555 | http://purl.obolibrary.org/obo/GO_0044228 | denotes | host cell surface |
T16 | 1544-1562 | http://purl.obolibrary.org/obo/GO_0044228 | denotes | host cell surfaces |
T17 | 543-555 | http://purl.obolibrary.org/obo/GO_0009986 | denotes | cell surface |
T18 | 1549-1562 | http://purl.obolibrary.org/obo/GO_0009986 | denotes | cell surfaces |
T19 | 1641-1651 | http://purl.obolibrary.org/obo/GO_0043226 | denotes | organelles |
T20 | 1768-1791 | http://purl.obolibrary.org/obo/GO_0020003 | denotes | parasitophorous vacuole |
T21 | 1784-1791 | http://purl.obolibrary.org/obo/GO_0005773 | denotes | vacuole |
EDAM-topics
Id | Subject | Object | Predicate | Lexical cue |
---|---|---|---|---|
T1 | 28-36 | http://edamontology.org/topic_0078 | denotes | proteins |
T2 | 174-180 | http://edamontology.org/topic_2815 | denotes | humans |
T3 | 223-231 | http://edamontology.org/topic_0783 | denotes | pathogen |
T4 | 521-530 | http://edamontology.org/topic_2839 | denotes | molecules |
T5 | 924-934 | http://edamontology.org/topic_3382 | denotes | microscopy |
T6 | 964-971 | http://edamontology.org/topic_0078 | denotes | protein |
T7 | 1064-1072 | http://edamontology.org/topic_0078 | denotes | proteins |
T8 | 1150-1157 | http://edamontology.org/topic_0078 | denotes | protein |
T9 | 1255-1263 | http://edamontology.org/topic_0078 | denotes | proteins |
T10 | 1373-1384 | http://edamontology.org/topic_0200 | denotes | microarrays |
T11 | 1373-1384 | http://edamontology.org/topic_3518 | denotes | microarrays |
T12 | 1441-1453 | http://edamontology.org/topic_0602 | denotes | interactions |
T13 | 1497-1505 | http://edamontology.org/topic_2830 | denotes | antigens |
T14 | 1641-1651 | http://edamontology.org/topic_0616 | denotes | organelles |
EDAM-DFO
Id | Subject | Object | Predicate | Lexical cue |
---|---|---|---|---|
T1 | 28-36 | http://edamontology.org/data_1467 | denotes | proteins |
T2 | 28-36 | http://edamontology.org/format_1208 | denotes | proteins |
T3 | 62-72 | http://edamontology.org/data_0883 | denotes | structures |
T4 | 223-231 | http://edamontology.org/data_3718 | denotes | pathogen |
T5 | 506-517 | http://edamontology.org/operation_2423 | denotes | recognition |
T6 | 569-577 | http://edamontology.org/data_2048 | denotes | reported |
T7 | 775-789 | http://edamontology.org/operation_0004 | denotes | functionalized |
T8 | 832-842 | http://edamontology.org/operation_0337 | denotes | visualized |
T9 | 952-958 | http://edamontology.org/data_2048 | denotes | report |
T10 | 964-971 | http://edamontology.org/data_1467 | denotes | protein |
T11 | 964-971 | http://edamontology.org/format_1208 | denotes | protein |
T12 | 964-982 | http://edamontology.org/operation_2997 | denotes | protein components |
T13 | 1064-1072 | http://edamontology.org/data_1467 | denotes | proteins |
T14 | 1064-1072 | http://edamontology.org/format_1208 | denotes | proteins |
T15 | 1150-1157 | http://edamontology.org/data_1467 | denotes | protein |
T16 | 1150-1157 | http://edamontology.org/format_1208 | denotes | protein |
T17 | 1255-1263 | http://edamontology.org/data_1467 | denotes | proteins |
T18 | 1255-1263 | http://edamontology.org/format_1208 | denotes | proteins |
T19 | 1598-1605 | http://edamontology.org/operation_2409 | denotes | process |
T20 | 1598-1605 | http://edamontology.org/operation_0004 | denotes | process |
Allie
Id | Subject | Object | Predicate | Lexical cue |
---|---|---|---|---|
SS1_22997241_4_0 | 709-727 | expanded | denotes | glycosaminoglycans |
SS2_22997241_4_0 | 729-733 | abbr | denotes | GAGs |
AE1_22997241_4_0 | SS1_22997241_4_0 | SS2_22997241_4_0 | abbreviatedTo | glycosaminoglycans,GAGs |
GlycoBiology-Motifs
Id | Subject | Object | Predicate | Lexical cue |
---|---|---|---|---|
T1 | 54-61 | http://rdf.glycoinfo.org/glycan/G54161DR | denotes | heparin |
T2 | 767-774 | http://rdf.glycoinfo.org/glycan/G54161DR | denotes | heparin |
T3 | 843-850 | http://rdf.glycoinfo.org/glycan/G54161DR | denotes | heparin |
T4 | 1182-1189 | http://rdf.glycoinfo.org/glycan/G54161DR | denotes | heparin |
T5 | 1276-1283 | http://rdf.glycoinfo.org/glycan/G54161DR | denotes | heparin |
T6 | 1288-1295 | http://rdf.glycoinfo.org/glycan/G54161DR | denotes | heparin |
T7 | 1349-1356 | http://rdf.glycoinfo.org/glycan/G54161DR | denotes | heparin |
GlycoBiology-Epitope
Id | Subject | Object | Predicate | Lexical cue |
---|---|---|---|---|
PD-GlycoEpitope-B_T1 | 744-759 | http://www.glycoepitope.jp/epitopes/EP0086 | denotes | heparan sulfate |
mondo_disease
Id | Subject | Object | Predicate | Lexical cue | mondo_id |
---|---|---|---|---|---|
T1 | 118-131 | Disease | denotes | toxoplasmosis | http://purl.obolibrary.org/obo/MONDO_0005989 |
T2 | 160-173 | Disease | denotes | infections in | http://purl.obolibrary.org/obo/MONDO_0005550 |
T3 | 1711-1720 | Disease | denotes | infection | http://purl.obolibrary.org/obo/MONDO_0005550 |
NCBITAXON
Id | Subject | Object | Predicate | Lexical cue | db_id |
---|---|---|---|---|---|
T1 | 0-17 | OrganismTaxon | denotes | Toxoplasma gondii | 5811 |
T2 | 74-91 | OrganismTaxon | denotes | Toxoplasma gondii | 5811 |
T3 | 263-280 | OrganismTaxon | denotes | Toxoplasma gondii | 5811 |
Anatomy-UBERON
Id | Subject | Object | Predicate | Lexical cue | uberon_id |
---|---|---|---|---|---|
T1 | 322-336 | Body_part | denotes | nucleated cell | http://purl.obolibrary.org/obo/CL_0002242 |
T2 | 1641-1651 | Body_part | denotes | organelles | http://purl.obolibrary.org/obo/GO_0043226 |
T3 | 1784-1791 | Body_part | denotes | vacuole | http://purl.obolibrary.org/obo/GO_0005773 |
CL-cell
Id | Subject | Object | Predicate | Lexical cue | cl_id |
---|---|---|---|---|---|
T1 | 322-336 | Cell | denotes | nucleated cell | http://purl.obolibrary.org/obo/CL:0002242 |