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LitCoin-sentences

Id Subject Object Predicate Lexical cue
T7 645-874 Sentence denotes Here we successfully constructed the desminopathy rat model, evaluated with conventional stains, containing hematoxylin and eosin (HE), Gomori Trichrome (MGT), (PAS), red oil (ORO), NADH-TR, SDH staining and immunohistochemistry.
T1 0-117 Sentence denotes Voltage-Dependent Anion Channel 1(VDAC1) Participates the Apoptosis of the Mitochondrial Dysfunction in Desminopathy.
T2 118-233 Sentence denotes Desminopathies caused by the mutation in the gene coding for desmin are genetically protein aggregation myopathies.
T3 234-335 Sentence denotes Mitochondrial dysfunction is one of pathological changes in the desminopathies at the earliest stage.
T4 336-424 Sentence denotes The molecular mechanisms of mitochondria dysfunction in desminopathies remain exclusive.
T5 425-545 Sentence denotes VDAC1 regulates mitochondrial uptake across the outer membrane and mitochondrial outer membrane permeabilization (MOMP).
T6 546-644 Sentence denotes Relationships between desminopathies and Voltage-dependent anion channel 1 (VDAC1) remain unclear.
T8 875-1066 Sentence denotes Immunofluorescence results showed that VDAC1 was accumulated in the desmin highly stained area of muscle fibers of desminopathy patients or desminopathy rat model compared to the normal ones.
T9 1067-1343 Sentence denotes Meanwhile apoptosis related proteins bax and ATF2 were involved in desminopathy patients and desminopathy rat model, but not bcl-2, bcl-xl or HK2.VDAC1 and desmin are closely relevant in the tissue splices of deminopathies patients and rats with desminopathy at protein lever.
T10 1344-1459 Sentence denotes Moreover, apoptotic proteins are also involved in the desminopathies, like bax, ATF2, but not bcl-2, bcl-xl or HK2.
T11 1460-1604 Sentence denotes This pathological analysis presents the correlation between VDAC1 and desmin, and apoptosis related proteins are correlated in the desminopathy.
T12 1605-1706 Sentence denotes Furthermore, we provide a rat model of desminopathy for the investigation of desmin related myopathy.

LitCoin-entities-OrganismTaxon-PD

Id Subject Object Predicate Lexical cue db_id
T1 695-698 OrganismTaxon denotes rat NCBItxid:10116|NCBItxid:10114
T3 1028-1031 OrganismTaxon denotes rat NCBItxid:10116|NCBItxid:10114
T5 1173-1176 OrganismTaxon denotes rat NCBItxid:10116|NCBItxid:10114
T7 1303-1307 OrganismTaxon denotes rats NCBItxid:10118|NCBItxid:10116|NCBItxid:10114
T10 1631-1634 OrganismTaxon denotes rat NCBItxid:10116|NCBItxid:10114

LitCoin-entities

Id Subject Object Predicate Lexical cue db_id
11837 0-33 GeneOrGeneProduct denotes Voltage-Dependent Anion Channel 1 NCBIGene:7416|NCBIGene:83529
11838 34-39 GeneOrGeneProduct denotes VDAC1 NCBIGene:7416|NCBIGene:83529
11839 75-100 DiseaseOrPhenotypicFeature denotes Mitochondrial Dysfunction MESH:D028361
11840 104-116 DiseaseOrPhenotypicFeature denotes Desminopathy MESH:C563319
11841 118-132 DiseaseOrPhenotypicFeature denotes Desminopathies MESH:C563319
11842 179-185 GeneOrGeneProduct denotes desmin NCBIGene:1674
11843 222-232 DiseaseOrPhenotypicFeature denotes myopathies MESH:D009135
11844 234-259 DiseaseOrPhenotypicFeature denotes Mitochondrial dysfunction MESH:D028361
11845 298-312 DiseaseOrPhenotypicFeature denotes desminopathies MESH:C563319
11846 364-388 DiseaseOrPhenotypicFeature denotes mitochondria dysfunction MESH:D028361
11847 392-406 DiseaseOrPhenotypicFeature denotes desminopathies MESH:C563319
11848 425-430 GeneOrGeneProduct denotes VDAC1 NCBIGene:7416
11849 568-582 DiseaseOrPhenotypicFeature denotes desminopathies MESH:C563319
11850 587-620 GeneOrGeneProduct denotes Voltage-dependent anion channel 1 NCBIGene:7416
11851 622-627 GeneOrGeneProduct denotes VDAC1 NCBIGene:7416
11852 682-694 DiseaseOrPhenotypicFeature denotes desminopathy MESH:C563319
11853 695-698 OrganismTaxon denotes rat NCBITaxon:10116
11854 914-919 GeneOrGeneProduct denotes VDAC1 NCBIGene:7416|NCBIGene:83529
11855 943-949 GeneOrGeneProduct denotes desmin NCBIGene:1674|NCBIGene:64362
11856 990-1002 DiseaseOrPhenotypicFeature denotes desminopathy MESH:C563319
11857 1003-1011 OrganismTaxon denotes patients NCBITaxon:9606
11858 1015-1027 DiseaseOrPhenotypicFeature denotes desminopathy MESH:C563319
11859 1028-1031 OrganismTaxon denotes rat NCBITaxon:10116
11860 1104-1107 GeneOrGeneProduct denotes bax NCBIGene:24887|NCBIGene:581
11861 1112-1116 GeneOrGeneProduct denotes ATF2 NCBIGene:1386|NCBIGene:81647
11862 1134-1146 DiseaseOrPhenotypicFeature denotes desminopathy MESH:C563319
11863 1147-1155 OrganismTaxon denotes patients NCBITaxon:9606
11864 1160-1172 DiseaseOrPhenotypicFeature denotes desminopathy MESH:C563319
11865 1173-1176 OrganismTaxon denotes rat NCBITaxon:10116
11866 1192-1197 GeneOrGeneProduct denotes bcl-2 NCBIGene:24224|NCBIGene:596
11867 1199-1205 GeneOrGeneProduct denotes bcl-xl NCBIGene:24888|NCBIGene:598
11868 1209-1212 GeneOrGeneProduct denotes HK2 NCBIGene:25059|NCBIGene:3099
11869 1213-1218 GeneOrGeneProduct denotes VDAC1 NCBIGene:7416|NCBIGene:83529
11870 1223-1229 GeneOrGeneProduct denotes desmin NCBIGene:1674|NCBIGene:64362
11871 1290-1298 OrganismTaxon denotes patients NCBITaxon:9606
11872 1303-1307 OrganismTaxon denotes rats NCBITaxon:10116
11873 1313-1325 DiseaseOrPhenotypicFeature denotes desminopathy MESH:C563319
11874 1398-1412 DiseaseOrPhenotypicFeature denotes desminopathies MESH:C563319
11875 1419-1422 GeneOrGeneProduct denotes bax NCBIGene:24887|NCBIGene:581
11876 1424-1428 GeneOrGeneProduct denotes ATF2 NCBIGene:1386|NCBIGene:81647
11877 1438-1443 GeneOrGeneProduct denotes bcl-2 NCBIGene:24224|NCBIGene:596
11878 1445-1451 GeneOrGeneProduct denotes bcl-xl NCBIGene:24888|NCBIGene:598
11879 1455-1458 GeneOrGeneProduct denotes HK2 NCBIGene:25059|NCBIGene:3099
11880 1520-1525 GeneOrGeneProduct denotes VDAC1 NCBIGene:7416|NCBIGene:83529
11881 1530-1536 GeneOrGeneProduct denotes desmin NCBIGene:1674|NCBIGene:64362
11882 1591-1603 DiseaseOrPhenotypicFeature denotes desminopathy MESH:C563319
11883 1631-1634 OrganismTaxon denotes rat NCBITaxon:10116
11884 1644-1656 DiseaseOrPhenotypicFeature denotes desminopathy MESH:C563319
11885 1682-1688 GeneOrGeneProduct denotes desmin NCBIGene:64362
11886 1697-1705 DiseaseOrPhenotypicFeature denotes myopathy MESH:D009135

LitCoin_Mondo

Id Subject Object Predicate Lexical cue mondo_id
T1 222-232 DiseaseOrPhenotypicFeature denotes myopathies 0005336
T2 1697-1705 DiseaseOrPhenotypicFeature denotes myopathy 0005336

LitCoin-GeneOrGeneProduct-v0

Id Subject Object Predicate Lexical cue
T1 0-31 GeneOrGeneProduct denotes Voltage-Dependent Anion Channel
T2 34-39 GeneOrGeneProduct denotes VDAC1
T3 58-67 GeneOrGeneProduct denotes Apoptosis
T4 75-88 GeneOrGeneProduct denotes Mitochondrial
T5 147-155 GeneOrGeneProduct denotes mutation
T6 179-185 GeneOrGeneProduct denotes desmin
T7 202-209 GeneOrGeneProduct denotes protein
T8 234-247 GeneOrGeneProduct denotes Mitochondrial
T9 364-376 GeneOrGeneProduct denotes mitochondria
T10 425-430 GeneOrGeneProduct denotes VDAC1
T11 431-440 GeneOrGeneProduct denotes regulates
T12 441-454 GeneOrGeneProduct denotes mitochondrial
T13 492-520 GeneOrGeneProduct denotes mitochondrial outer membrane
T14 587-620 GeneOrGeneProduct denotes Voltage-dependent anion channel 1
T15 622-627 GeneOrGeneProduct denotes VDAC1
T16 636-643 GeneOrGeneProduct denotes unclear
T17 812-815 GeneOrGeneProduct denotes red
T18 827-831 GeneOrGeneProduct denotes NADH
T19 914-919 GeneOrGeneProduct denotes VDAC1
T20 943-949 GeneOrGeneProduct denotes desmin
T21 950-956 GeneOrGeneProduct denotes highly
T22 965-969 GeneOrGeneProduct denotes area
T23 973-979 GeneOrGeneProduct denotes muscle
T24 980-986 GeneOrGeneProduct denotes fibers
T25 1077-1086 GeneOrGeneProduct denotes apoptosis
T26 1087-1103 GeneOrGeneProduct denotes related proteins
T27 1112-1116 GeneOrGeneProduct denotes ATF2
T28 1192-1197 GeneOrGeneProduct denotes bcl-2
T29 1199-1205 GeneOrGeneProduct denotes bcl-xl
T30 1209-1212 GeneOrGeneProduct denotes HK2
T31 1213-1218 GeneOrGeneProduct denotes VDAC1
T32 1223-1229 GeneOrGeneProduct denotes desmin
T33 1265-1272 GeneOrGeneProduct denotes splices
T34 1329-1336 GeneOrGeneProduct denotes protein
T35 1364-1372 GeneOrGeneProduct denotes proteins
T36 1414-1418 GeneOrGeneProduct denotes like
T37 1424-1428 GeneOrGeneProduct denotes ATF2
T38 1438-1443 GeneOrGeneProduct denotes bcl-2
T39 1445-1451 GeneOrGeneProduct denotes bcl-xl
T40 1455-1458 GeneOrGeneProduct denotes HK2
T41 1520-1525 GeneOrGeneProduct denotes VDAC1
T42 1530-1536 GeneOrGeneProduct denotes desmin
T43 1542-1551 GeneOrGeneProduct denotes apoptosis
T44 1552-1568 GeneOrGeneProduct denotes related proteins
T45 1629-1634 GeneOrGeneProduct denotes a rat
T46 1682-1688 GeneOrGeneProduct denotes desmin

LitCoin-GeneOrGeneProduct-v2

Id Subject Object Predicate Lexical cue
T1 0-31 GeneOrGeneProduct denotes Voltage-Dependent Anion Channel
T2 34-39 GeneOrGeneProduct denotes VDAC1
T3 58-67 GeneOrGeneProduct denotes Apoptosis
T4 75-88 GeneOrGeneProduct denotes Mitochondrial
T5 179-185 GeneOrGeneProduct denotes desmin
T6 202-209 GeneOrGeneProduct denotes protein
T7 234-247 GeneOrGeneProduct denotes Mitochondrial
T8 364-376 GeneOrGeneProduct denotes mitochondria
T9 425-430 GeneOrGeneProduct denotes VDAC1
T10 441-454 GeneOrGeneProduct denotes mitochondrial
T11 492-520 GeneOrGeneProduct denotes mitochondrial outer membrane
T12 587-620 GeneOrGeneProduct denotes Voltage-dependent anion channel 1
T13 622-627 GeneOrGeneProduct denotes VDAC1
T14 636-643 GeneOrGeneProduct denotes unclear
T15 827-831 GeneOrGeneProduct denotes NADH
T16 914-919 GeneOrGeneProduct denotes VDAC1
T17 943-949 GeneOrGeneProduct denotes desmin
T18 965-969 GeneOrGeneProduct denotes area
T19 973-979 GeneOrGeneProduct denotes muscle
T20 1077-1086 GeneOrGeneProduct denotes apoptosis
T21 1087-1103 GeneOrGeneProduct denotes related proteins
T22 1112-1116 GeneOrGeneProduct denotes ATF2
T23 1192-1197 GeneOrGeneProduct denotes bcl-2
T24 1199-1205 GeneOrGeneProduct denotes bcl-xl
T25 1209-1212 GeneOrGeneProduct denotes HK2
T26 1213-1218 GeneOrGeneProduct denotes VDAC1
T27 1223-1229 GeneOrGeneProduct denotes desmin
T28 1329-1336 GeneOrGeneProduct denotes protein
T29 1414-1418 GeneOrGeneProduct denotes like
T30 1424-1428 GeneOrGeneProduct denotes ATF2
T31 1438-1443 GeneOrGeneProduct denotes bcl-2
T32 1445-1451 GeneOrGeneProduct denotes bcl-xl
T33 1455-1458 GeneOrGeneProduct denotes HK2
T34 1520-1525 GeneOrGeneProduct denotes VDAC1
T35 1530-1536 GeneOrGeneProduct denotes desmin
T36 1542-1551 GeneOrGeneProduct denotes apoptosis
T37 1552-1568 GeneOrGeneProduct denotes related proteins
T38 1682-1688 GeneOrGeneProduct denotes desmin

LitCoin-Disease-MeSH

Id Subject Object Predicate Lexical cue originalLabel
T1 222-232 DiseaseOrPhenotypicFeature denotes myopathies D009135
T2 1682-1705 DiseaseOrPhenotypicFeature denotes desmin related myopathy C563319

LitCoin-GeneOrGeneProduct-v3

Id Subject Object Predicate Lexical cue
T1 0-31 GeneOrGeneProduct denotes Voltage-Dependent Anion Channel
T2 34-39 GeneOrGeneProduct denotes VDAC1
T3 179-185 GeneOrGeneProduct denotes desmin
T4 425-430 GeneOrGeneProduct denotes VDAC1
T5 492-520 GeneOrGeneProduct denotes mitochondrial outer membrane
T6 587-620 GeneOrGeneProduct denotes Voltage-dependent anion channel 1
T7 622-627 GeneOrGeneProduct denotes VDAC1
T8 827-831 GeneOrGeneProduct denotes NADH
T9 914-919 GeneOrGeneProduct denotes VDAC1
T10 943-949 GeneOrGeneProduct denotes desmin
T11 1077-1103 GeneOrGeneProduct denotes apoptosis related proteins
T12 1112-1116 GeneOrGeneProduct denotes ATF2
T13 1192-1197 GeneOrGeneProduct denotes bcl-2
T14 1199-1205 GeneOrGeneProduct denotes bcl-xl
T15 1213-1218 GeneOrGeneProduct denotes VDAC1
T16 1223-1229 GeneOrGeneProduct denotes desmin
T17 1424-1428 GeneOrGeneProduct denotes ATF2
T18 1438-1443 GeneOrGeneProduct denotes bcl-2
T19 1445-1451 GeneOrGeneProduct denotes bcl-xl
T20 1520-1525 GeneOrGeneProduct denotes VDAC1
T21 1530-1536 GeneOrGeneProduct denotes desmin
T22 1542-1568 GeneOrGeneProduct denotes apoptosis related proteins
T23 1682-1688 GeneOrGeneProduct denotes desmin

LitCoin_Mondo_095

Id Subject Object Predicate Lexical cue mondo_id
T1 104-116 DiseaseOrPhenotypicFeature denotes Desminopathy 0011076
T2 682-694 DiseaseOrPhenotypicFeature denotes desminopathy 0011076
T3 806-809 DiseaseOrPhenotypicFeature denotes PAS 0004277
T4 990-1002 DiseaseOrPhenotypicFeature denotes desminopathy 0011076
T5 1015-1027 DiseaseOrPhenotypicFeature denotes desminopathy 0011076
T6 1134-1146 DiseaseOrPhenotypicFeature denotes desminopathy 0011076
T7 1160-1172 DiseaseOrPhenotypicFeature denotes desminopathy 0011076
T8 1313-1325 DiseaseOrPhenotypicFeature denotes desminopathy 0011076
T9 1591-1603 DiseaseOrPhenotypicFeature denotes desminopathy 0011076
T10 1644-1656 DiseaseOrPhenotypicFeature denotes desminopathy 0011076
T11 1682-1705 DiseaseOrPhenotypicFeature denotes desmin related myopathy 0011076

LitCoin-MeSH-Disease-2

Id Subject Object Predicate Lexical cue ID:
T1 75-100 DiseaseOrPhenotypicFeature denotes Mitochondrial Dysfunction DISEASE
T2 104-116 DiseaseOrPhenotypicFeature denotes Desminopathy DISEASE
T3 118-132 DiseaseOrPhenotypicFeature denotes Desminopathies DISEASE
T4 222-232 DiseaseOrPhenotypicFeature denotes myopathies D009135
T5 234-259 DiseaseOrPhenotypicFeature denotes Mitochondrial dysfunction DISEASE
T6 298-312 DiseaseOrPhenotypicFeature denotes desminopathies DISEASE
T7 364-388 DiseaseOrPhenotypicFeature denotes mitochondria dysfunction DISEASE
T8 392-406 DiseaseOrPhenotypicFeature denotes desminopathies DISEASE
T9 568-582 DiseaseOrPhenotypicFeature denotes desminopathies DISEASE
T10 682-694 DiseaseOrPhenotypicFeature denotes desminopathy DISEASE
T11 990-1002 DiseaseOrPhenotypicFeature denotes desminopathy DISEASE
T12 1015-1027 DiseaseOrPhenotypicFeature denotes desminopathy DISEASE
T13 1134-1146 DiseaseOrPhenotypicFeature denotes desminopathy DISEASE
T14 1160-1172 DiseaseOrPhenotypicFeature denotes desminopathy DISEASE
T15 1313-1325 DiseaseOrPhenotypicFeature denotes desminopathy DISEASE
T16 1398-1412 DiseaseOrPhenotypicFeature denotes desminopathies DISEASE
T17 1591-1603 DiseaseOrPhenotypicFeature denotes desminopathy DISEASE
T18 1644-1656 DiseaseOrPhenotypicFeature denotes desminopathy DISEASE
T19 1682-1705 DiseaseOrPhenotypicFeature denotes desmin related myopathy C563319

LitCoin-MONDO_bioort2019

Id Subject Object Predicate Lexical cue #label
T1 75-100 DiseaseOrPhenotypicFeature denotes Mitochondrial Dysfunction DISEASE
T2 104-116 DiseaseOrPhenotypicFeature denotes Desminopathy DISEASE
T3 118-132 DiseaseOrPhenotypicFeature denotes Desminopathies DISEASE
T4 222-232 DiseaseOrPhenotypicFeature denotes myopathies D009135
T5 234-259 DiseaseOrPhenotypicFeature denotes Mitochondrial dysfunction DISEASE
T6 298-312 DiseaseOrPhenotypicFeature denotes desminopathies DISEASE
T7 364-388 DiseaseOrPhenotypicFeature denotes mitochondria dysfunction DISEASE
T8 392-406 DiseaseOrPhenotypicFeature denotes desminopathies DISEASE
T9 568-582 DiseaseOrPhenotypicFeature denotes desminopathies DISEASE
T10 682-694 DiseaseOrPhenotypicFeature denotes desminopathy DISEASE
T11 990-1002 DiseaseOrPhenotypicFeature denotes desminopathy DISEASE
T12 1015-1027 DiseaseOrPhenotypicFeature denotes desminopathy DISEASE
T13 1134-1146 DiseaseOrPhenotypicFeature denotes desminopathy DISEASE
T14 1160-1172 DiseaseOrPhenotypicFeature denotes desminopathy DISEASE
T15 1313-1325 DiseaseOrPhenotypicFeature denotes desminopathy DISEASE
T16 1398-1412 DiseaseOrPhenotypicFeature denotes desminopathies DISEASE
T17 1591-1603 DiseaseOrPhenotypicFeature denotes desminopathy DISEASE
T18 1644-1656 DiseaseOrPhenotypicFeature denotes desminopathy DISEASE
T19 1682-1705 DiseaseOrPhenotypicFeature denotes desmin related myopathy C563319

LitCoin-Chemical-MeSH-CHEBI

Id Subject Object Predicate Lexical cue ID:
T1 18-23 ChemicalEntity denotes Anion http://purl.obolibrary.org/obo/CHEBI_22563
T2 605-610 ChemicalEntity denotes anion D000838|http://purl.obolibrary.org/obo/CHEBI_22563
T4 753-764 ChemicalEntity denotes hematoxylin D006416|http://purl.obolibrary.org/obo/CHEBI_51686
T6 769-774 ChemicalEntity denotes eosin D004801
T7 806-809 ChemicalEntity denotes PAS http://purl.obolibrary.org/obo/CHEBI_27565
T8 827-831 ChemicalEntity denotes NADH http://purl.obolibrary.org/obo/CHEBI_57945|http://purl.obolibrary.org/obo/CHEBI_16908

LitCoin-NCBITaxon-2

Id Subject Object Predicate Lexical cue
T1 695-698 OrganismTaxon denotes rat
T2 1003-1011 OrganismTaxon denotes patients
T3 1028-1031 OrganismTaxon denotes rat
T4 1147-1155 OrganismTaxon denotes patients
T5 1173-1176 OrganismTaxon denotes rat
T6 1290-1298 OrganismTaxon denotes patients
T7 1303-1307 OrganismTaxon denotes rats
T8 1631-1634 OrganismTaxon denotes rat

LitCoin-training-merged

Id Subject Object Predicate Lexical cue #label ID:
T8 827-831 ChemicalEntity denotes NADH http://purl.obolibrary.org/obo/CHEBI_16908|http://purl.obolibrary.org/obo/CHEBI_57945
T7 806-809 ChemicalEntity denotes PAS http://purl.obolibrary.org/obo/CHEBI_27565
T6 769-774 ChemicalEntity denotes eosin D004801
T4 753-764 ChemicalEntity denotes hematoxylin http://purl.obolibrary.org/obo/CHEBI_51686|D006416
T2 605-610 ChemicalEntity denotes anion http://purl.obolibrary.org/obo/CHEBI_22563|D000838
T1 18-23 ChemicalEntity denotes Anion http://purl.obolibrary.org/obo/CHEBI_22563
T23 1682-1688 GeneOrGeneProduct denotes desmin
T22 1542-1568 GeneOrGeneProduct denotes apoptosis related proteins
T21 1530-1536 GeneOrGeneProduct denotes desmin
T20 1520-1525 GeneOrGeneProduct denotes VDAC1
T19 1445-1451 GeneOrGeneProduct denotes bcl-xl
T18 1438-1443 GeneOrGeneProduct denotes bcl-2
T17 1424-1428 GeneOrGeneProduct denotes ATF2
T16 1223-1229 GeneOrGeneProduct denotes desmin
T15 1213-1218 GeneOrGeneProduct denotes VDAC1
T14 1199-1205 GeneOrGeneProduct denotes bcl-xl
T13 1192-1197 GeneOrGeneProduct denotes bcl-2
T12 1112-1116 GeneOrGeneProduct denotes ATF2
T11 1077-1103 GeneOrGeneProduct denotes apoptosis related proteins
T10 943-949 GeneOrGeneProduct denotes desmin
T9 914-919 GeneOrGeneProduct denotes VDAC1
T80316 827-831 GeneOrGeneProduct denotes NADH
T49575 622-627 GeneOrGeneProduct denotes VDAC1
T16807 587-620 GeneOrGeneProduct denotes Voltage-dependent anion channel 1
T5 492-520 GeneOrGeneProduct denotes mitochondrial outer membrane
T93316 425-430 GeneOrGeneProduct denotes VDAC1
T3 179-185 GeneOrGeneProduct denotes desmin
T62371 34-39 GeneOrGeneProduct denotes VDAC1
T39875 0-31 GeneOrGeneProduct denotes Voltage-Dependent Anion Channel
T8740 1682-1705 DiseaseOrPhenotypicFeature denotes desmin related myopathy C563319
T43200 1644-1656 DiseaseOrPhenotypicFeature denotes desminopathy DISEASE
T16626 1591-1603 DiseaseOrPhenotypicFeature denotes desminopathy DISEASE
T22579 1398-1412 DiseaseOrPhenotypicFeature denotes desminopathies DISEASE
T29217 1313-1325 DiseaseOrPhenotypicFeature denotes desminopathy DISEASE
T22423 1160-1172 DiseaseOrPhenotypicFeature denotes desminopathy DISEASE
T97368 1134-1146 DiseaseOrPhenotypicFeature denotes desminopathy DISEASE
T97719 1015-1027 DiseaseOrPhenotypicFeature denotes desminopathy DISEASE
T63845 990-1002 DiseaseOrPhenotypicFeature denotes desminopathy DISEASE
T73672 682-694 DiseaseOrPhenotypicFeature denotes desminopathy DISEASE
T32772 568-582 DiseaseOrPhenotypicFeature denotes desminopathies DISEASE
T89467 392-406 DiseaseOrPhenotypicFeature denotes desminopathies DISEASE
T22028 364-388 DiseaseOrPhenotypicFeature denotes mitochondria dysfunction DISEASE
T81697 298-312 DiseaseOrPhenotypicFeature denotes desminopathies DISEASE
T37086 234-259 DiseaseOrPhenotypicFeature denotes Mitochondrial dysfunction DISEASE
T48284 222-232 DiseaseOrPhenotypicFeature denotes myopathies D009135
T43059 118-132 DiseaseOrPhenotypicFeature denotes Desminopathies DISEASE
T69632 104-116 DiseaseOrPhenotypicFeature denotes Desminopathy DISEASE
T45830 75-100 DiseaseOrPhenotypicFeature denotes Mitochondrial Dysfunction DISEASE
T44530 1631-1634 OrganismTaxon denotes rat
T90357 1303-1307 OrganismTaxon denotes rats
T10555 1290-1298 OrganismTaxon denotes patients
T98653 1173-1176 OrganismTaxon denotes rat
T69327 1147-1155 OrganismTaxon denotes patients
T22728 1028-1031 OrganismTaxon denotes rat
T6852 1003-1011 OrganismTaxon denotes patients
T32246 695-698 OrganismTaxon denotes rat