PubMed:26153105
Annnotations
CL-cell
Id | Subject | Object | Predicate | Lexical cue | cl_id |
---|---|---|---|---|---|
T1 | 35-52 | Cell | denotes | neural stem cells | http://purl.obolibrary.org/obo/CL:0000047 |
T2 | 138-154 | Cell | denotes | Neural stem cell | http://purl.obolibrary.org/obo/CL:0000047 |
T3 | 145-154 | Cell | denotes | stem cell | http://purl.obolibrary.org/obo/CL:0000034 |
T4 | 156-159 | Cell | denotes | NSC | http://purl.obolibrary.org/obo/CL:0000047 |
T5 | 813-818 | Cell | denotes | HCELL | http://purl.obolibrary.org/obo/CL:0002674 |
T6 | 820-838 | Cell | denotes | hematopoietic cell | http://purl.obolibrary.org/obo/CL:0000988 |
T7 | 903-914 | Cell | denotes | neural cell | http://purl.obolibrary.org/obo/CL:0002319 |
T8 | 1135-1138 | Cell | denotes | NSC | http://purl.obolibrary.org/obo/CL:0000047 |
T9 | 1359-1368 | Cell | denotes | stem cell | http://purl.obolibrary.org/obo/CL:0000034 |
T10 | 1406-1409 | Cell | denotes | NSC | http://purl.obolibrary.org/obo/CL:0000047 |
T11 | 1447-1457 | Cell | denotes | stem cells | http://purl.obolibrary.org/obo/CL:0000034 |
T12 | 1520-1536 | Cell | denotes | progenitor cells | http://purl.obolibrary.org/obo/CL:0011026 |
T13 | 1655-1664 | Cell | denotes | stem cell | http://purl.obolibrary.org/obo/CL:0000034 |
T14 | 1769-1784 | Cell | denotes | progenitor cell | http://purl.obolibrary.org/obo/CL:0011026 |
T15 | 1870-1873 | Cell | denotes | NSC | http://purl.obolibrary.org/obo/CL:0000047 |
Inflammaging
Id | Subject | Object | Predicate | Lexical cue |
---|---|---|---|---|
T1 | 0-137 | Sentence | denotes | Cell surface glycan engineering of neural stem cells augments neurotropism and improves recovery in a murine model of multiple sclerosis. |
T2 | 138-283 | Sentence | denotes | Neural stem cell (NSC)-based therapies offer potential for neural repair in central nervous system (CNS) inflammatory and degenerative disorders. |
T3 | 284-474 | Sentence | denotes | Typically, these conditions present with multifocal CNS lesions making it impractical to inject NSCs locally, thus mandating optimization of vascular delivery of the cells to involved sites. |
T4 | 475-623 | Sentence | denotes | Here, we analyzed NSCs for expression of molecular effectors of cell migration and found that these cells are natively devoid of E-selectin ligands. |
T5 | 624-944 | Sentence | denotes | Using glycosyltransferase-programmed stereosubstitution (GPS), we glycan engineered the cell surface of NSCs ("GPS-NSCs") with resultant enforced expression of the potent E-selectin ligand HCELL (hematopoietic cell E-/L-selectin ligand) and of an E-selectin-binding glycoform of neural cell adhesion molecule ("NCAM-E"). |
T6 | 945-1112 | Sentence | denotes | Following intravenous (i.v.) injection, short-term homing studies demonstrated that, compared with buffer-treated (control) NSCs, GPS-NSCs showed greater neurotropism. |
T7 | 1113-1381 | Sentence | denotes | Administration of GPS-NSC significantly attenuated the clinical course of experimental autoimmune encephalomyelitis (EAE), with markedly decreased inflammation and improved oligodendroglial and axonal integrity, but without evidence of long-term stem cell engraftment. |
T8 | 1382-1573 | Sentence | denotes | Notably, this effect of NSC is not a universal property of adult stem cells, as administration of GPS-engineered mouse hematopoietic stem/progenitor cells did not improve EAE clinical course. |
T9 | 1574-1899 | Sentence | denotes | These findings highlight the utility of cell surface glycan engineering to boost stem cell delivery in neuroinflammatory conditions and indicate that, despite the use of a neural tissue-specific progenitor cell population, neural repair in EAE results from endogenous repair and not from direct, NSC-derived cell replacement. |
T1 | 0-137 | Sentence | denotes | Cell surface glycan engineering of neural stem cells augments neurotropism and improves recovery in a murine model of multiple sclerosis. |
T2 | 138-283 | Sentence | denotes | Neural stem cell (NSC)-based therapies offer potential for neural repair in central nervous system (CNS) inflammatory and degenerative disorders. |
T3 | 284-474 | Sentence | denotes | Typically, these conditions present with multifocal CNS lesions making it impractical to inject NSCs locally, thus mandating optimization of vascular delivery of the cells to involved sites. |
T4 | 475-623 | Sentence | denotes | Here, we analyzed NSCs for expression of molecular effectors of cell migration and found that these cells are natively devoid of E-selectin ligands. |
T5 | 624-944 | Sentence | denotes | Using glycosyltransferase-programmed stereosubstitution (GPS), we glycan engineered the cell surface of NSCs ("GPS-NSCs") with resultant enforced expression of the potent E-selectin ligand HCELL (hematopoietic cell E-/L-selectin ligand) and of an E-selectin-binding glycoform of neural cell adhesion molecule ("NCAM-E"). |
T6 | 945-1112 | Sentence | denotes | Following intravenous (i.v.) injection, short-term homing studies demonstrated that, compared with buffer-treated (control) NSCs, GPS-NSCs showed greater neurotropism. |
T7 | 1113-1381 | Sentence | denotes | Administration of GPS-NSC significantly attenuated the clinical course of experimental autoimmune encephalomyelitis (EAE), with markedly decreased inflammation and improved oligodendroglial and axonal integrity, but without evidence of long-term stem cell engraftment. |
T8 | 1382-1573 | Sentence | denotes | Notably, this effect of NSC is not a universal property of adult stem cells, as administration of GPS-engineered mouse hematopoietic stem/progenitor cells did not improve EAE clinical course. |
T9 | 1574-1899 | Sentence | denotes | These findings highlight the utility of cell surface glycan engineering to boost stem cell delivery in neuroinflammatory conditions and indicate that, despite the use of a neural tissue-specific progenitor cell population, neural repair in EAE results from endogenous repair and not from direct, NSC-derived cell replacement. |
PubMed_ArguminSci
Id | Subject | Object | Predicate | Lexical cue |
---|---|---|---|---|
T1 | 138-283 | DRI_Background | denotes | Neural stem cell (NSC)-based therapies offer potential for neural repair in central nervous system (CNS) inflammatory and degenerative disorders. |
T2 | 284-474 | DRI_Challenge | denotes | Typically, these conditions present with multifocal CNS lesions making it impractical to inject NSCs locally, thus mandating optimization of vascular delivery of the cells to involved sites. |
T3 | 475-623 | DRI_Outcome | denotes | Here, we analyzed NSCs for expression of molecular effectors of cell migration and found that these cells are natively devoid of E-selectin ligands. |
T4 | 624-629 | DRI_Approach | denotes | Using |
T5 | 680-870 | DRI_Approach | denotes | (GPS), we glycan engineered the cell surface of NSCs ("GPS-NSCs") with resultant enforced expression of the potent E-selectin ligand HCELL (hematopoietic cell E-/L-selectin ligand) and of an |
T6 | 900-944 | DRI_Approach | denotes | of neural cell adhesion molecule ("NCAM-E"). |
T7 | 974-1112 | DRI_Background | denotes | injection, short-term homing studies demonstrated that, compared with buffer-treated (control) NSCs, GPS-NSCs showed greater neurotropism. |
T8 | 1113-1381 | DRI_Background | denotes | Administration of GPS-NSC significantly attenuated the clinical course of experimental autoimmune encephalomyelitis (EAE), with markedly decreased inflammation and improved oligodendroglial and axonal integrity, but without evidence of long-term stem cell engraftment. |
T9 | 1382-1573 | DRI_Background | denotes | Notably, this effect of NSC is not a universal property of adult stem cells, as administration of GPS-engineered mouse hematopoietic stem/progenitor cells did not improve EAE clinical course. |
T10 | 1574-1899 | DRI_Background | denotes | These findings highlight the utility of cell surface glycan engineering to boost stem cell delivery in neuroinflammatory conditions and indicate that, despite the use of a neural tissue-specific progenitor cell population, neural repair in EAE results from endogenous repair and not from direct, NSC-derived cell replacement. |
Glycosmos6-MAT
Id | Subject | Object | Predicate | Lexical cue |
---|---|---|---|---|
T1 | 42-52 | http://purl.obolibrary.org/obo/MAT_0000185 | denotes | stem cells |
T2 | 42-46 | http://purl.obolibrary.org/obo/MAT_0000239 | denotes | stem |
T3 | 145-154 | http://purl.obolibrary.org/obo/MAT_0000185 | denotes | stem cell |
T4 | 145-149 | http://purl.obolibrary.org/obo/MAT_0000239 | denotes | stem |
T5 | 214-236 | http://purl.obolibrary.org/obo/MAT_0000457 | denotes | central nervous system |
T6 | 222-236 | http://purl.obolibrary.org/obo/MAT_0000026 | denotes | nervous system |
T7 | 238-241 | http://purl.obolibrary.org/obo/MAT_0000457 | denotes | CNS |
T8 | 336-339 | http://purl.obolibrary.org/obo/MAT_0000457 | denotes | CNS |
T9 | 1359-1368 | http://purl.obolibrary.org/obo/MAT_0000185 | denotes | stem cell |
T10 | 1359-1363 | http://purl.obolibrary.org/obo/MAT_0000239 | denotes | stem |
T11 | 1447-1457 | http://purl.obolibrary.org/obo/MAT_0000185 | denotes | stem cells |
T12 | 1447-1451 | http://purl.obolibrary.org/obo/MAT_0000239 | denotes | stem |
T13 | 1515-1519 | http://purl.obolibrary.org/obo/MAT_0000239 | denotes | stem |
T14 | 1655-1664 | http://purl.obolibrary.org/obo/MAT_0000185 | denotes | stem cell |
T15 | 1655-1659 | http://purl.obolibrary.org/obo/MAT_0000239 | denotes | stem |
sentences
Id | Subject | Object | Predicate | Lexical cue |
---|---|---|---|---|
TextSentencer_T1 | 0-137 | Sentence | denotes | Cell surface glycan engineering of neural stem cells augments neurotropism and improves recovery in a murine model of multiple sclerosis. |
TextSentencer_T2 | 138-283 | Sentence | denotes | Neural stem cell (NSC)-based therapies offer potential for neural repair in central nervous system (CNS) inflammatory and degenerative disorders. |
TextSentencer_T3 | 284-474 | Sentence | denotes | Typically, these conditions present with multifocal CNS lesions making it impractical to inject NSCs locally, thus mandating optimization of vascular delivery of the cells to involved sites. |
TextSentencer_T4 | 475-623 | Sentence | denotes | Here, we analyzed NSCs for expression of molecular effectors of cell migration and found that these cells are natively devoid of E-selectin ligands. |
TextSentencer_T5 | 624-944 | Sentence | denotes | Using glycosyltransferase-programmed stereosubstitution (GPS), we glycan engineered the cell surface of NSCs ("GPS-NSCs") with resultant enforced expression of the potent E-selectin ligand HCELL (hematopoietic cell E-/L-selectin ligand) and of an E-selectin-binding glycoform of neural cell adhesion molecule ("NCAM-E"). |
TextSentencer_T6 | 945-1112 | Sentence | denotes | Following intravenous (i.v.) injection, short-term homing studies demonstrated that, compared with buffer-treated (control) NSCs, GPS-NSCs showed greater neurotropism. |
TextSentencer_T7 | 1113-1381 | Sentence | denotes | Administration of GPS-NSC significantly attenuated the clinical course of experimental autoimmune encephalomyelitis (EAE), with markedly decreased inflammation and improved oligodendroglial and axonal integrity, but without evidence of long-term stem cell engraftment. |
TextSentencer_T8 | 1382-1573 | Sentence | denotes | Notably, this effect of NSC is not a universal property of adult stem cells, as administration of GPS-engineered mouse hematopoietic stem/progenitor cells did not improve EAE clinical course. |
TextSentencer_T9 | 1574-1899 | Sentence | denotes | These findings highlight the utility of cell surface glycan engineering to boost stem cell delivery in neuroinflammatory conditions and indicate that, despite the use of a neural tissue-specific progenitor cell population, neural repair in EAE results from endogenous repair and not from direct, NSC-derived cell replacement. |
T1 | 0-137 | Sentence | denotes | Cell surface glycan engineering of neural stem cells augments neurotropism and improves recovery in a murine model of multiple sclerosis. |
T2 | 138-283 | Sentence | denotes | Neural stem cell (NSC)-based therapies offer potential for neural repair in central nervous system (CNS) inflammatory and degenerative disorders. |
T3 | 284-474 | Sentence | denotes | Typically, these conditions present with multifocal CNS lesions making it impractical to inject NSCs locally, thus mandating optimization of vascular delivery of the cells to involved sites. |
T4 | 475-623 | Sentence | denotes | Here, we analyzed NSCs for expression of molecular effectors of cell migration and found that these cells are natively devoid of E-selectin ligands. |
T5 | 624-944 | Sentence | denotes | Using glycosyltransferase-programmed stereosubstitution (GPS), we glycan engineered the cell surface of NSCs ("GPS-NSCs") with resultant enforced expression of the potent E-selectin ligand HCELL (hematopoietic cell E-/L-selectin ligand) and of an E-selectin-binding glycoform of neural cell adhesion molecule ("NCAM-E"). |
T6 | 945-1112 | Sentence | denotes | Following intravenous (i.v.) injection, short-term homing studies demonstrated that, compared with buffer-treated (control) NSCs, GPS-NSCs showed greater neurotropism. |
T7 | 1113-1381 | Sentence | denotes | Administration of GPS-NSC significantly attenuated the clinical course of experimental autoimmune encephalomyelitis (EAE), with markedly decreased inflammation and improved oligodendroglial and axonal integrity, but without evidence of long-term stem cell engraftment. |
T8 | 1382-1573 | Sentence | denotes | Notably, this effect of NSC is not a universal property of adult stem cells, as administration of GPS-engineered mouse hematopoietic stem/progenitor cells did not improve EAE clinical course. |
T9 | 1574-1899 | Sentence | denotes | These findings highlight the utility of cell surface glycan engineering to boost stem cell delivery in neuroinflammatory conditions and indicate that, despite the use of a neural tissue-specific progenitor cell population, neural repair in EAE results from endogenous repair and not from direct, NSC-derived cell replacement. |
T1 | 0-137 | Sentence | denotes | Cell surface glycan engineering of neural stem cells augments neurotropism and improves recovery in a murine model of multiple sclerosis. |
T2 | 138-283 | Sentence | denotes | Neural stem cell (NSC)-based therapies offer potential for neural repair in central nervous system (CNS) inflammatory and degenerative disorders. |
T3 | 284-474 | Sentence | denotes | Typically, these conditions present with multifocal CNS lesions making it impractical to inject NSCs locally, thus mandating optimization of vascular delivery of the cells to involved sites. |
T4 | 475-623 | Sentence | denotes | Here, we analyzed NSCs for expression of molecular effectors of cell migration and found that these cells are natively devoid of E-selectin ligands. |
T5 | 624-944 | Sentence | denotes | Using glycosyltransferase-programmed stereosubstitution (GPS), we glycan engineered the cell surface of NSCs ("GPS-NSCs") with resultant enforced expression of the potent E-selectin ligand HCELL (hematopoietic cell E-/L-selectin ligand) and of an E-selectin-binding glycoform of neural cell adhesion molecule ("NCAM-E"). |
T6 | 945-1112 | Sentence | denotes | Following intravenous (i.v.) injection, short-term homing studies demonstrated that, compared with buffer-treated (control) NSCs, GPS-NSCs showed greater neurotropism. |
T7 | 1113-1381 | Sentence | denotes | Administration of GPS-NSC significantly attenuated the clinical course of experimental autoimmune encephalomyelitis (EAE), with markedly decreased inflammation and improved oligodendroglial and axonal integrity, but without evidence of long-term stem cell engraftment. |
T8 | 1382-1573 | Sentence | denotes | Notably, this effect of NSC is not a universal property of adult stem cells, as administration of GPS-engineered mouse hematopoietic stem/progenitor cells did not improve EAE clinical course. |
T9 | 1574-1899 | Sentence | denotes | These findings highlight the utility of cell surface glycan engineering to boost stem cell delivery in neuroinflammatory conditions and indicate that, despite the use of a neural tissue-specific progenitor cell population, neural repair in EAE results from endogenous repair and not from direct, NSC-derived cell replacement. |
ICD10
Id | Subject | Object | Predicate | Lexical cue |
---|---|---|---|---|
T1 | 118-136 | http://purl.bioontology.org/ontology/ICD10/G35 | denotes | multiple sclerosis |
T2 | 214-236 | http://purl.bioontology.org/ontology/ICD10/B69.0 | denotes | central nervous system |
T3 | 214-236 | http://purl.bioontology.org/ontology/ICD10/G96.9 | denotes | central nervous system |
T4 | 222-229 | http://purl.bioontology.org/ontology/ICD10/R45.0 | denotes | nervous |
T5 | 434-442 | http://purl.bioontology.org/ontology/ICD10/O80-O84.9 | denotes | delivery |
T6 | 1665-1673 | http://purl.bioontology.org/ontology/ICD10/O80-O84.9 | denotes | delivery |
GlycoBiology-FMA
Id | Subject | Object | Predicate | Lexical cue |
---|---|---|---|---|
_T1 | 0-12 | FMAID:212684 | denotes | Cell surface |
_T2 | 0-12 | FMAID:200942 | denotes | Cell surface |
_T3 | 5-12 | FMAID:146300 | denotes | surface |
_T4 | 5-12 | FMAID:50594 | denotes | surface |
_T5 | 35-52 | FMAID:171175 | denotes | neural stem cells |
_T6 | 35-52 | FMAID:86684 | denotes | neural stem cells |
_T7 | 35-52 | FMAID:201610 | denotes | neural stem cells |
_T8 | 35-52 | FMAID:70333 | denotes | neural stem cells |
_T9 | 42-52 | FMAID:167693 | denotes | stem cells |
_T10 | 42-52 | FMAID:63368 | denotes | stem cells |
_T11 | 47-52 | FMAID:169002 | denotes | cells |
_T12 | 47-52 | FMAID:68646 | denotes | cells |
_T13 | 138-154 | FMAID:171175 | denotes | Neural stem cell |
_T14 | 138-154 | FMAID:201610 | denotes | Neural stem cell |
_T15 | 138-154 | FMAID:70333 | denotes | Neural stem cell |
_T16 | 138-154 | FMAID:86684 | denotes | Neural stem cell |
_T17 | 145-154 | FMAID:167693 | denotes | stem cell |
_T18 | 145-154 | FMAID:63368 | denotes | stem cell |
_T19 | 214-221 | FMAID:30328 | denotes | central |
_T20 | 214-221 | FMAID:242678 | denotes | central |
_T21 | 214-221 | FMAID:174816 | denotes | central |
_T22 | 214-236 | FMAID:165583 | denotes | central nervous system |
_T23 | 214-236 | FMAID:180408 | denotes | central nervous system |
_T24 | 214-236 | FMAID:180409 | denotes | central nervous system |
_T25 | 214-236 | FMAID:272591 | denotes | central nervous system |
_T26 | 222-236 | FMAID:7157 | denotes | nervous system |
_T27 | 222-236 | FMAID:93586 | denotes | nervous system |
_T28 | 238-241 | FMAID:265384 | denotes | CNS |
_T29 | 336-339 | FMAID:265384 | denotes | CNS |
_T30 | 450-455 | FMAID:169002 | denotes | cells |
_T31 | 450-455 | FMAID:68646 | denotes | cells |
_T32 | 575-580 | FMAID:169002 | denotes | cells |
_T33 | 575-580 | FMAID:68646 | denotes | cells |
_T34 | 604-614 | FMAID:62932 | denotes | E-selectin |
_T35 | 604-614 | FMAID:167267 | denotes | E-selectin |
_T36 | 604-614 | FMAID:167265 | denotes | E-selectin |
_T37 | 604-614 | FMAID:62931 | denotes | E-selectin |
_T38 | 604-614 | FMAID:167268 | denotes | E-selectin |
_T39 | 604-614 | FMAID:62933 | denotes | E-selectin |
_T40 | 606-614 | FMAID:61795 | denotes | selectin |
_T41 | 606-614 | FMAID:165243 | denotes | selectin |
_T42 | 712-724 | FMAID:212684 | denotes | cell surface |
_T43 | 712-724 | FMAID:200942 | denotes | cell surface |
_T44 | 717-724 | FMAID:50594 | denotes | surface |
_T45 | 717-724 | FMAID:146300 | denotes | surface |
_T46 | 795-805 | FMAID:167265 | denotes | E-selectin |
_T47 | 795-805 | FMAID:62933 | denotes | E-selectin |
_T48 | 795-805 | FMAID:62932 | denotes | E-selectin |
_T49 | 795-805 | FMAID:167268 | denotes | E-selectin |
_T50 | 795-805 | FMAID:62931 | denotes | E-selectin |
_T51 | 795-805 | FMAID:167267 | denotes | E-selectin |
_T52 | 797-805 | FMAID:165243 | denotes | selectin |
_T53 | 797-805 | FMAID:61795 | denotes | selectin |
_T54 | 820-838 | FMAID:83598 | denotes | hematopoietic cell |
_T55 | 820-838 | FMAID:197894 | denotes | hematopoietic cell |
_T56 | 820-838 | FMAID:197893 | denotes | hematopoietic cell |
_T57 | 820-838 | FMAID:201460 | denotes | hematopoietic cell |
_T58 | 839-852 | FMAID:62932 | denotes | E-/L-selectin |
_T59 | 839-852 | FMAID:167267 | denotes | E-/L-selectin |
_T60 | 842-852 | FMAID:62931 | denotes | L-selectin |
_T61 | 842-852 | FMAID:167265 | denotes | L-selectin |
_T62 | 842-852 | FMAID:167268 | denotes | L-selectin |
_T63 | 842-852 | FMAID:62933 | denotes | L-selectin |
_T64 | 844-852 | FMAID:165243 | denotes | selectin |
_T65 | 844-852 | FMAID:61795 | denotes | selectin |
_T66 | 871-881 | FMAID:62932 | denotes | E-selectin |
_T67 | 871-881 | FMAID:62931 | denotes | E-selectin |
_T68 | 871-881 | FMAID:167265 | denotes | E-selectin |
_T69 | 871-881 | FMAID:167267 | denotes | E-selectin |
_T70 | 871-881 | FMAID:167268 | denotes | E-selectin |
_T71 | 871-881 | FMAID:62933 | denotes | E-selectin |
_T72 | 873-881 | FMAID:61795 | denotes | selectin |
_T73 | 873-881 | FMAID:165243 | denotes | selectin |
_T74 | 903-932 | FMAID:165776 | denotes | neural cell adhesion molecule |
_T75 | 903-932 | FMAID:67856 | denotes | neural cell adhesion molecule |
_T76 | 910-932 | FMAID:67214 | denotes | cell adhesion molecule |
_T77 | 910-932 | FMAID:167237 | denotes | cell adhesion molecule |
_T78 | 910-932 | FMAID:165233 | denotes | cell adhesion molecule |
_T79 | 910-932 | FMAID:167238 | denotes | cell adhesion molecule |
_T80 | 910-932 | FMAID:62914 | denotes | cell adhesion molecule |
_T81 | 910-932 | FMAID:62915 | denotes | cell adhesion molecule |
_T82 | 1286-1302 | FMAID:197925 | denotes | oligodendroglial |
_T83 | 1286-1302 | FMAID:150813 | denotes | oligodendroglial |
_T84 | 1286-1302 | FMAID:83665 | denotes | oligodendroglial |
_T85 | 1307-1313 | FMAID:67308 | denotes | axonal |
_T86 | 1307-1313 | FMAID:165274 | denotes | axonal |
_T87 | 1359-1368 | FMAID:167693 | denotes | stem cell |
_T88 | 1359-1368 | FMAID:63368 | denotes | stem cell |
_T89 | 1447-1457 | FMAID:167693 | denotes | stem cells |
_T90 | 1447-1457 | FMAID:63368 | denotes | stem cells |
_T91 | 1452-1457 | FMAID:68646 | denotes | cells |
_T92 | 1452-1457 | FMAID:169002 | denotes | cells |
_T93 | 1501-1519 | FMAID:9667 | denotes | hematopoietic stem |
_T94 | 1501-1519 | FMAID:201460 | denotes | hematopoietic stem |
_T95 | 1501-1519 | FMAID:97578 | denotes | hematopoietic stem |
_T96 | 1531-1536 | FMAID:68646 | denotes | cells |
_T97 | 1531-1536 | FMAID:169002 | denotes | cells |
_T98 | 1614-1626 | FMAID:200942 | denotes | cell surface |
_T99 | 1614-1626 | FMAID:212684 | denotes | cell surface |
_T100 | 1619-1626 | FMAID:146300 | denotes | surface |
_T101 | 1619-1626 | FMAID:50594 | denotes | surface |
_T102 | 1655-1664 | FMAID:167693 | denotes | stem cell |
_T103 | 1655-1664 | FMAID:63368 | denotes | stem cell |
_T104 | 1746-1759 | FMAID:256076 | denotes | neural tissue |
_T105 | 1753-1759 | FMAID:256050 | denotes | tissue |
uniprot-human
Id | Subject | Object | Predicate | Lexical cue |
---|---|---|---|---|
T1 | 604-614 | http://www.uniprot.org/uniprot/P16581 | denotes | E-selectin |
T2 | 795-805 | http://www.uniprot.org/uniprot/P16581 | denotes | E-selectin |
T3 | 871-881 | http://www.uniprot.org/uniprot/P16581 | denotes | E-selectin |
T4 | 604-622 | http://www.uniprot.org/uniprot/Q92896 | denotes | E-selectin ligands |
T5 | 795-812 | http://www.uniprot.org/uniprot/Q92896 | denotes | E-selectin ligand |
T6 | 844-872 | http://www.uniprot.org/uniprot/Q92896 | denotes | selectin ligand) and of an E |
T7 | 842-852 | http://www.uniprot.org/uniprot/P14151 | denotes | L-selectin |
T8 | 842-859 | http://www.uniprot.org/uniprot/Q8NCG5 | denotes | L-selectin ligand |
T9 | 910-932 | http://www.uniprot.org/uniprot/P16422 | denotes | cell adhesion molecule |
T10 | 910-932 | http://www.uniprot.org/uniprot/P43121 | denotes | cell adhesion molecule |
T11 | 910-932 | http://www.uniprot.org/uniprot/Q14CZ8 | denotes | cell adhesion molecule |
T12 | 910-932 | http://www.uniprot.org/uniprot/Q8N126 | denotes | cell adhesion molecule |
T13 | 910-932 | http://www.uniprot.org/uniprot/Q8NFZ8 | denotes | cell adhesion molecule |
T14 | 910-932 | http://www.uniprot.org/uniprot/P50895 | denotes | cell adhesion molecule |
T15 | 910-932 | http://www.uniprot.org/uniprot/Q8N3J6 | denotes | cell adhesion molecule |
T16 | 910-932 | http://www.uniprot.org/uniprot/Q8N2F4 | denotes | cell adhesion molecule |
T17 | 910-932 | http://www.uniprot.org/uniprot/Q92823 | denotes | cell adhesion molecule |
T18 | 935-939 | http://www.uniprot.org/uniprot/Q59FL7 | denotes | NCAM |
uniprot-mouse
Id | Subject | Object | Predicate | Lexical cue |
---|---|---|---|---|
T1 | 604-614 | http://www.uniprot.org/uniprot/Q00690 | denotes | E-selectin |
T2 | 795-805 | http://www.uniprot.org/uniprot/Q00690 | denotes | E-selectin |
T3 | 871-881 | http://www.uniprot.org/uniprot/Q00690 | denotes | E-selectin |
T4 | 842-852 | http://www.uniprot.org/uniprot/P18337 | denotes | L-selectin |
GlycoBiology-NCBITAXON
Id | Subject | Object | Predicate | Lexical cue |
---|---|---|---|---|
T1 | 47-52 | http://purl.bioontology.org/ontology/STY/T025 | denotes | cells |
T2 | 450-455 | http://purl.bioontology.org/ontology/STY/T025 | denotes | cells |
T3 | 575-580 | http://purl.bioontology.org/ontology/STY/T025 | denotes | cells |
T4 | 991-995 | http://purl.bioontology.org/ontology/NCBITAXON/62951 | denotes | term |
T5 | 1354-1358 | http://purl.bioontology.org/ontology/NCBITAXON/62951 | denotes | term |
T6 | 1452-1457 | http://purl.bioontology.org/ontology/STY/T025 | denotes | cells |
T7 | 1531-1536 | http://purl.bioontology.org/ontology/STY/T025 | denotes | cells |
T8 | 1580-1588 | http://purl.bioontology.org/ontology/STY/T033 | denotes | findings |
T9 | 1753-1759 | http://purl.bioontology.org/ontology/STY/T024 | denotes | tissue |
GO-BP
Id | Subject | Object | Predicate | Lexical cue |
---|---|---|---|---|
T1 | 385-392 | http://purl.obolibrary.org/obo/GO_0051179 | denotes | locally |
T2 | 539-553 | http://purl.obolibrary.org/obo/GO_0016477 | denotes | cell migration |
T3 | 910-923 | http://purl.obolibrary.org/obo/GO_0007155 | denotes | cell adhesion |
T4 | 910-932 | http://purl.obolibrary.org/obo/GO_0060352 | denotes | cell adhesion molecule |
T5 | 910-932 | http://purl.obolibrary.org/obo/GO_0007155 | denotes | cell adhesion molecule |
T6 | 1260-1272 | http://purl.obolibrary.org/obo/GO_0006954 | denotes | inflammation |
GO-MF
Id | Subject | Object | Predicate | Lexical cue |
---|---|---|---|---|
T1 | 606-614 | http://purl.obolibrary.org/obo/GO_0030246 | denotes | selectin |
T2 | 797-805 | http://purl.obolibrary.org/obo/GO_0030246 | denotes | selectin |
T3 | 844-852 | http://purl.obolibrary.org/obo/GO_0030246 | denotes | selectin |
T4 | 873-881 | http://purl.obolibrary.org/obo/GO_0030246 | denotes | selectin |
T5 | 615-622 | http://purl.obolibrary.org/obo/GO_0005488 | denotes | ligands |
T6 | 806-812 | http://purl.obolibrary.org/obo/GO_0005488 | denotes | ligand |
T7 | 853-859 | http://purl.obolibrary.org/obo/GO_0005488 | denotes | ligand |
T8 | 882-889 | http://purl.obolibrary.org/obo/GO_0070026 | denotes | binding |
T9 | 882-889 | http://purl.obolibrary.org/obo/GO_0003680 | denotes | binding |
T10 | 882-889 | http://purl.obolibrary.org/obo/GO_0017091 | denotes | binding |
T11 | 882-889 | http://purl.obolibrary.org/obo/GO_0005488 | denotes | binding |
GO-CC
Id | Subject | Object | Predicate | Lexical cue |
---|---|---|---|---|
T1 | 0-4 | http://purl.obolibrary.org/obo/GO_0005623 | denotes | Cell |
T2 | 47-52 | http://purl.obolibrary.org/obo/GO_0005623 | denotes | cells |
T3 | 450-455 | http://purl.obolibrary.org/obo/GO_0005623 | denotes | cells |
T4 | 575-580 | http://purl.obolibrary.org/obo/GO_0005623 | denotes | cells |
T5 | 1452-1457 | http://purl.obolibrary.org/obo/GO_0005623 | denotes | cells |
T6 | 150-154 | http://purl.obolibrary.org/obo/GO_0005623 | denotes | cell |
T7 | 539-543 | http://purl.obolibrary.org/obo/GO_0005623 | denotes | cell |
T8 | 712-716 | http://purl.obolibrary.org/obo/GO_0005623 | denotes | cell |
T9 | 834-838 | http://purl.obolibrary.org/obo/GO_0005623 | denotes | cell |
T10 | 910-914 | http://purl.obolibrary.org/obo/GO_0005623 | denotes | cell |
T11 | 1364-1368 | http://purl.obolibrary.org/obo/GO_0005623 | denotes | cell |
T12 | 1614-1618 | http://purl.obolibrary.org/obo/GO_0005623 | denotes | cell |
T13 | 1660-1664 | http://purl.obolibrary.org/obo/GO_0005623 | denotes | cell |
T14 | 1780-1784 | http://purl.obolibrary.org/obo/GO_0005623 | denotes | cell |
T15 | 1882-1886 | http://purl.obolibrary.org/obo/GO_0005623 | denotes | cell |
T16 | 0-12 | http://purl.obolibrary.org/obo/GO_0009986 | denotes | Cell surface |
T17 | 712-724 | http://purl.obolibrary.org/obo/GO_0009986 | denotes | cell surface |
T18 | 1614-1626 | http://purl.obolibrary.org/obo/GO_0009986 | denotes | cell surface |
UBERON-AE
Id | Subject | Object | Predicate | Lexical cue |
---|---|---|---|---|
T1 | 214-221 | http://purl.obolibrary.org/obo/UBERON_0012131 | denotes | central |
T2 | 214-236 | http://purl.obolibrary.org/obo/UBERON_0001017 | denotes | central nervous system |
T3 | 222-236 | http://purl.obolibrary.org/obo/UBERON_0001016 | denotes | nervous system |
T4 | 1746-1759 | http://purl.obolibrary.org/obo/UBERON_0003714 | denotes | neural tissue |
T5 | 1753-1759 | http://purl.obolibrary.org/obo/UBERON_0000479 | denotes | tissue |
GlycoBiology-MAT
Id | Subject | Object | Predicate | Lexical cue |
---|---|---|---|---|
T1 | 42-46 | http://purl.obolibrary.org/obo/MAT_0000239 | denotes | stem |
T2 | 42-52 | http://purl.obolibrary.org/obo/MAT_0000185 | denotes | stem cells |
T3 | 145-149 | http://purl.obolibrary.org/obo/MAT_0000239 | denotes | stem |
T4 | 145-154 | http://purl.obolibrary.org/obo/MAT_0000185 | denotes | stem cell |
T5 | 214-236 | http://purl.obolibrary.org/obo/MAT_0000457 | denotes | central nervous system |
T6 | 222-236 | http://purl.obolibrary.org/obo/MAT_0000026 | denotes | nervous system |
T7 | 1359-1363 | http://purl.obolibrary.org/obo/MAT_0000239 | denotes | stem |
T8 | 1359-1368 | http://purl.obolibrary.org/obo/MAT_0000185 | denotes | stem cell |
T9 | 1447-1451 | http://purl.obolibrary.org/obo/MAT_0000239 | denotes | stem |
T10 | 1447-1457 | http://purl.obolibrary.org/obo/MAT_0000185 | denotes | stem cells |
T11 | 1515-1519 | http://purl.obolibrary.org/obo/MAT_0000239 | denotes | stem |
T12 | 1655-1659 | http://purl.obolibrary.org/obo/MAT_0000239 | denotes | stem |
T13 | 1655-1664 | http://purl.obolibrary.org/obo/MAT_0000185 | denotes | stem cell |
Lectin
Id | Subject | Object | Predicate | Lexical cue |
---|---|---|---|---|
Lectin_T1 | 606-614 | https://acgg.asia/db/lfdb/LfDB0013 | denotes | selectin |
Lectin_T2 | 797-805 | https://acgg.asia/db/lfdb/LfDB0013 | denotes | selectin |
Lectin_T3 | 844-852 | https://acgg.asia/db/lfdb/LfDB0013 | denotes | selectin |
Lectin_T4 | 873-881 | https://acgg.asia/db/lfdb/LfDB0013 | denotes | selectin |
Lectin_T5 | 604-614 | https://acgg.asia/db/lfdb/LfDB0043 | denotes | E-selectin |
Lectin_T6 | 795-805 | https://acgg.asia/db/lfdb/LfDB0043 | denotes | E-selectin |
Lectin_T7 | 844-852 | https://acgg.asia/db/lfdb/LfDB0043 | denotes | selectin |
Lectin_T8 | 871-881 | https://acgg.asia/db/lfdb/LfDB0043 | denotes | E-selectin |
Lectin_T9 | 606-614 | https://acgg.asia/db/lfdb/LfDB0142 | denotes | selectin |
Lectin_T10 | 797-805 | https://acgg.asia/db/lfdb/LfDB0142 | denotes | selectin |
Lectin_T11 | 842-852 | https://acgg.asia/db/lfdb/LfDB0142 | denotes | L-selectin |
Lectin_T12 | 873-881 | https://acgg.asia/db/lfdb/LfDB0142 | denotes | selectin |
performance-test
Id | Subject | Object | Predicate | Lexical cue |
---|---|---|---|---|
PD-UBERON-AE-B_T1 | 1753-1759 | http://purl.obolibrary.org/obo/UBERON_0000479 | denotes | tissue |
PD-UBERON-AE-B_T2 | 214-221 | http://purl.obolibrary.org/obo/UBERON_0012131 | denotes | central |
PD-UBERON-AE-B_T3 | 214-236 | http://purl.obolibrary.org/obo/UBERON_0001017 | denotes | central nervous system |
PD-UBERON-AE-B_T4 | 222-236 | http://purl.obolibrary.org/obo/UBERON_0001016 | denotes | nervous system |
PD-UBERON-AE-B_T5 | 1501-1519 | http://purl.obolibrary.org/obo/UBERON_0002390 | denotes | hematopoietic stem |
PD-UBERON-AE-B_T6 | 1746-1759 | http://purl.obolibrary.org/obo/UBERON_0003714 | denotes | neural tissue |
mondo_disease
Id | Subject | Object | Predicate | Lexical cue | mondo_id |
---|---|---|---|---|---|
T1 | 118-136 | Disease | denotes | multiple sclerosis | http://purl.obolibrary.org/obo/MONDO_0005301 |
T2 | 156-159 | Disease | denotes | NSC | http://purl.obolibrary.org/obo/MONDO_0018816 |
T3 | 260-282 | Disease | denotes | degenerative disorders | http://purl.obolibrary.org/obo/MONDO_0024236 |
T4 | 681-684 | Disease | denotes | GPS | http://purl.obolibrary.org/obo/MONDO_0007686 |
T5 | 735-738 | Disease | denotes | GPS | http://purl.obolibrary.org/obo/MONDO_0007686 |
T6 | 1075-1078 | Disease | denotes | GPS | http://purl.obolibrary.org/obo/MONDO_0007686 |
T7 | 1131-1134 | Disease | denotes | GPS | http://purl.obolibrary.org/obo/MONDO_0007686 |
T8 | 1135-1138 | Disease | denotes | NSC | http://purl.obolibrary.org/obo/MONDO_0018816 |
T9 | 1187-1228 | Disease | denotes | experimental autoimmune encephalomyelitis | http://purl.obolibrary.org/obo/MONDO_0005134 |
T10 | 1230-1233 | Disease | denotes | EAE | http://purl.obolibrary.org/obo/MONDO_0005134 |
T11 | 1260-1272 | Disease | denotes | inflammation | http://purl.obolibrary.org/obo/MONDO_0021166 |
T12 | 1406-1409 | Disease | denotes | NSC | http://purl.obolibrary.org/obo/MONDO_0018816 |
T13 | 1480-1483 | Disease | denotes | GPS | http://purl.obolibrary.org/obo/MONDO_0007686 |
T14 | 1553-1556 | Disease | denotes | EAE | http://purl.obolibrary.org/obo/MONDO_0005134 |
T15 | 1814-1817 | Disease | denotes | EAE | http://purl.obolibrary.org/obo/MONDO_0005134 |
T16 | 1870-1873 | Disease | denotes | NSC | http://purl.obolibrary.org/obo/MONDO_0018816 |
NCBITAXON
Id | Subject | Object | Predicate | Lexical cue | db_id |
---|---|---|---|---|---|
T1 | 1495-1500 | OrganismTaxon | denotes | mouse | 10088|10090 |
Anatomy-MAT
Id | Subject | Object | Predicate | Lexical cue | mat_id |
---|---|---|---|---|---|
T1 | 42-52 | Body_part | denotes | stem cells | http://purl.obolibrary.org/obo/MAT_0000185 |
T2 | 145-154 | Body_part | denotes | stem cell | http://purl.obolibrary.org/obo/MAT_0000185 |
T3 | 214-236 | Body_part | denotes | central nervous system | http://purl.obolibrary.org/obo/MAT_0000457 |
T4 | 238-241 | Body_part | denotes | CNS | http://purl.obolibrary.org/obo/MAT_0000457 |
T5 | 336-339 | Body_part | denotes | CNS | http://purl.obolibrary.org/obo/MAT_0000457 |
T6 | 1359-1368 | Body_part | denotes | stem cell | http://purl.obolibrary.org/obo/MAT_0000185 |
T7 | 1447-1457 | Body_part | denotes | stem cells | http://purl.obolibrary.org/obo/MAT_0000185 |
T8 | 1515-1519 | Body_part | denotes | stem | http://purl.obolibrary.org/obo/MAT_0000239 |
T9 | 1655-1664 | Body_part | denotes | stem cell | http://purl.obolibrary.org/obo/MAT_0000185 |
Anatomy-UBERON
Id | Subject | Object | Predicate | Lexical cue | uberon_id |
---|---|---|---|---|---|
T1 | 42-52 | Body_part | denotes | stem cells | http://purl.obolibrary.org/obo/CL_0000034 |
T2 | 145-154 | Body_part | denotes | stem cell | http://purl.obolibrary.org/obo/CL_0000034 |
T3 | 214-236 | Body_part | denotes | central nervous system | http://purl.obolibrary.org/obo/UBERON_0001017 |
T4 | 238-241 | Body_part | denotes | CNS | http://purl.obolibrary.org/obo/UBERON_0001017 |
T5 | 336-339 | Body_part | denotes | CNS | http://purl.obolibrary.org/obo/UBERON_0001017 |
T6 | 820-838 | Body_part | denotes | hematopoietic cell | http://purl.obolibrary.org/obo/CL_0000988 |
T7 | 903-914 | Body_part | denotes | neural cell | http://purl.obolibrary.org/obo/CL_0002319 |
T8 | 1359-1368 | Body_part | denotes | stem cell | http://purl.obolibrary.org/obo/CL_0000034 |
T9 | 1447-1457 | Body_part | denotes | stem cells | http://purl.obolibrary.org/obo/CL_0000034 |
T10 | 1520-1536 | Body_part | denotes | progenitor cells | http://purl.obolibrary.org/obo/CL_0011026 |
T11 | 1655-1664 | Body_part | denotes | stem cell | http://purl.obolibrary.org/obo/CL_0000034 |
T12 | 1746-1759 | Body_part | denotes | neural tissue | http://purl.obolibrary.org/obo/UBERON_0003714 |
T13 | 1769-1784 | Body_part | denotes | progenitor cell | http://purl.obolibrary.org/obo/CL_0011026 |