PMC:5097349 / 1363-16093 JSONTXT 2 Projects

Annnotations TAB TSV DIC JSON TextAE

Id Subject Object Predicate Lexical cue hp_id
T4 68-98 Phenotype denotes central nervous system disease http://purl.obolibrary.org/obo/HP_0002011
T5 527-543 Phenotype denotes rosenthal fibers http://purl.obolibrary.org/obo/HP_0100320
T6 1022-1035 Phenotype denotes limb weakness http://purl.obolibrary.org/obo/HP_0003690
T7 1295-1301 Phenotype denotes ataxia http://purl.obolibrary.org/obo/HP_0001251
T8 1303-1313 Phenotype denotes dysarthria http://purl.obolibrary.org/obo/HP_0001260
T9 1315-1325 Phenotype denotes depression http://purl.obolibrary.org/obo/HP_0000716
T10 1413-1427 Phenotype denotes muscle atrophy http://purl.obolibrary.org/obo/HP_0003202
T11 2714-2724 Phenotype denotes dysarthria http://purl.obolibrary.org/obo/HP_0001260
T12 2745-2754 Phenotype denotes nystagmus http://purl.obolibrary.org/obo/HP_0000639
T13 2767-2775 Phenotype denotes Myokymia http://purl.obolibrary.org/obo/HP_0002411
T14 2857-2873 Phenotype denotes muscular atrophy http://purl.obolibrary.org/obo/HP_0003202
T15 3056-3079 Phenotype denotes positive Babinski signs http://purl.obolibrary.org/obo/HP_0003487
T16 3107-3113 Phenotype denotes Ataxia http://purl.obolibrary.org/obo/HP_0001251
T17 3194-3214 Phenotype denotes extrapyramidal signs http://purl.obolibrary.org/obo/HP_0002071
T18 3529-3538 Phenotype denotes hepatitis http://purl.obolibrary.org/obo/HP_0012115
T19 4621-4639 Phenotype denotes cerebellar atrophy http://purl.obolibrary.org/obo/HP_0001272
T20 4692-4739 Phenotype denotes abnormality in the periventricular white matter http://purl.obolibrary.org/obo/HP_0002518
T21 5434-5452 Phenotype denotes cerebellar atrophy http://purl.obolibrary.org/obo/HP_0001272
T22 7085-7091 Phenotype denotes ataxia http://purl.obolibrary.org/obo/HP_0001251
T23 7221-7238 Phenotype denotes Palatal myoclonus http://purl.obolibrary.org/obo/HP_0010530
T24 7420-7441 Phenotype denotes autonomic dysfunction http://purl.obolibrary.org/obo/HP_0012332
T25 7482-7505 Phenotype denotes orthostatic hypotension http://purl.obolibrary.org/obo/HP_0001278
T26 7897-7939 Phenotype denotes periventricular white matter abnormalities http://purl.obolibrary.org/obo/HP_0002518
T27 8459-8475 Phenotype denotes rosenthal fibers http://purl.obolibrary.org/obo/HP_0100320
T28 8987-9003 Phenotype denotes leukodystrophies http://purl.obolibrary.org/obo/HP_0002415
T29 9120-9136 Phenotype denotes leukodystrophies http://purl.obolibrary.org/obo/HP_0002415
T30 9296-9310 Phenotype denotes leukodystrophy http://purl.obolibrary.org/obo/HP_0002415
T31 9359-9375 Phenotype denotes cortical atrophy http://purl.obolibrary.org/obo/HP_0002120
T32 9411-9423 Phenotype denotes tetraparesis http://purl.obolibrary.org/obo/HP_0002273
T33 9435-9443 Phenotype denotes seizures http://purl.obolibrary.org/obo/HP_0001250
T34 9445-9463 Phenotype denotes cortical blindness http://purl.obolibrary.org/obo/HP_0100704
T35 9557-9565 Phenotype denotes migraine http://purl.obolibrary.org/obo/HP_0002076
T36 9571-9579 Phenotype denotes dementia http://purl.obolibrary.org/obo/HP_0000726
T37 9589-9626 Phenotype denotes enlargement of the lateral ventricles http://purl.obolibrary.org/obo/HP_0006956
T38 9647-9665 Phenotype denotes behavioral changes http://purl.obolibrary.org/obo/HP_0000708
T39 9667-9675 Phenotype denotes dementia http://purl.obolibrary.org/obo/HP_0000726
T40 9695-9703 Phenotype denotes epilepsy http://purl.obolibrary.org/obo/HP_0001250
T41 9801-9807 Phenotype denotes ataxia http://purl.obolibrary.org/obo/HP_0001251
T42 9862-9875 Phenotype denotes xanthomatosis http://purl.obolibrary.org/obo/HP_0000991
T43 9888-9902 Phenotype denotes polyneuropathy http://purl.obolibrary.org/obo/HP_0001271
T44 9911-9922 Phenotype denotes xanthomatas http://purl.obolibrary.org/obo/HP_0000991
T45 9987-10005 Phenotype denotes cerebellar atrophy http://purl.obolibrary.org/obo/HP_0001272
T46 10028-10039 Phenotype denotes memory loss http://purl.obolibrary.org/obo/HP_0002354
T47 10041-10049 Phenotype denotes dementia http://purl.obolibrary.org/obo/HP_0000726
T48 10051-10073 Phenotype denotes skeletal abnormalities http://purl.obolibrary.org/obo/HP_0000924
T49 10090-10106 Phenotype denotes cortical atrophy http://purl.obolibrary.org/obo/HP_0002120
T50 10127-10136 Phenotype denotes migraines http://purl.obolibrary.org/obo/HP_0002076
T51 10143-10150 Phenotype denotes strokes http://purl.obolibrary.org/obo/HP_0001297
T52 10255-10262 Phenotype denotes strokes http://purl.obolibrary.org/obo/HP_0001297
T53 10394-10400 Phenotype denotes ataxia http://purl.obolibrary.org/obo/HP_0001251
T54 10446-10473 Phenotype denotes diffuse leukoencephalopathy http://purl.obolibrary.org/obo/HP_0006994
T55 10612-10626 Phenotype denotes leukodystrophy http://purl.obolibrary.org/obo/HP_0002415
T56 10716-10735 Phenotype denotes leukoencephalopathy http://purl.obolibrary.org/obo/HP_0002352
T57 10740-10759 Phenotype denotes spastic paraparesis http://purl.obolibrary.org/obo/HP_0002313
T58 10790-10808 Phenotype denotes pseudobulbar palsy http://purl.obolibrary.org/obo/HP_0007024
T59 10870-10887 Phenotype denotes cognitive decline http://purl.obolibrary.org/obo/HP_0001268
T60 10950-10973 Phenotype denotes orthostatic hypotension http://purl.obolibrary.org/obo/HP_0001278
T61 11001-11018 Phenotype denotes cerebellar ataxia http://purl.obolibrary.org/obo/HP_0001251
T62 11024-11050 Phenotype denotes transient ischemic attacks http://purl.obolibrary.org/obo/HP_0002326
T63 11057-11081 Phenotype denotes peripheral demyelinating http://purl.obolibrary.org/obo/HP_0011096
T64 11082-11096 Phenotype denotes polyneuropathy http://purl.obolibrary.org/obo/HP_0001271
T65 11952-11976 Phenotype denotes white matter abnormality http://purl.obolibrary.org/obo/HP_0002500
T66 12778-12792 Phenotype denotes leukodystrophy http://purl.obolibrary.org/obo/HP_0002415
T67 13046-13062 Phenotype denotes rosenthal fibers http://purl.obolibrary.org/obo/HP_0100320
T68 13098-13103 Phenotype denotes shock http://purl.obolibrary.org/obo/HP_0031273