> top > projects > sonoma2 > docs > PubMed:30643024 > annotations
sonoma2  

PubMed:30643024 JSONTXT 27 Projects

Annnotations TAB TSV DIC JSON TextAE Lectin_function IAV-Glycan

Id Subject Object Predicate Lexical cue
T0 0-45 DISEASE denotes Neurodegenerative Charcot-Marie-Tooth disease
T1 149-154 DISEASE denotes aaRSs
T2 313-318 DISEASE denotes aaRSs
T3 342-352 REG denotes implicated
T4 418-424 REG denotes common
T5 425-440 GENE denotes aaRS-associated
T6 477-502 DISEASE denotes neurodegenerative disease
T7 503-533 DISEASE denotes Charcot-Marie-Tooth neuropathy
T8 535-538 DISEASE denotes CMT
T9 541-547 REG denotes caused
T10 573-582 VAR denotes mutations
T11 586-591 DISEASE denotes aaRSs
T12 627-632 GENE denotes GlyRS
T13 634-639 GENE denotes TyrRS
T14 641-646 GENE denotes AlaRS
T15 648-653 GENE denotes HisRS
T16 655-660 GENE denotes TrpRS
T17 666-671 GENE denotes MetRS
T18 674-679 DISEASE denotes aaRSs
T19 731-734 DISEASE denotes CMT
T20 781-786 DISEASE denotes aaRSs
T21 790-793 DISEASE denotes CMT
T22 847-855 NEGREG denotes impaired
T23 861-869 MPA denotes charging
T24 971-980 VAR denotes mutations
T25 984-989 DISEASE denotes aaRSs
T26 1005-1009 GENE denotes aaRS
T27 1014-1021 VAR denotes mutants
T28 1032-1036 NEGREG denotes loss
T29 1040-1068 MPA denotes tRNA aminoacylation function
T30 1121-1130 VAR denotes mutations
T31 1134-1139 GENE denotes GlyRS
T32 1140-1145 REG denotes cause
T33 1146-1149 DISEASE denotes CMT
T34 1164-1180 POSREG denotes gain-of-function
T35 1220-1235 DISEASE denotes aaRS-linked CMT
T36 1232-1235 DISEASE denotes CMT
T37 1465-1470 DISEASE denotes aaRSs
T38 1476-1486 DISEASE denotes neuropathy
T39 1530-1535 DISEASE denotes aaRSs
T40 1755-1770 DISEASE denotes aaRS-linked CMT
T41 1767-1770 DISEASE denotes CMT
T42 1856-1861 DISEASE denotes aaRSs
T43 1886-1901 DISEASE denotes aaRS-linked CMT
T44 1898-1901 DISEASE denotes CMT
R0 T7 T3 ThemeOf Charcot-Marie-Tooth neuropathy,implicated
R1 T7 T4 ThemeOf Charcot-Marie-Tooth neuropathy,common
R10 T19 T4 ThemeOf CMT,common
R11 T23 T22 ThemeOf charging,impaired
R12 T27 T28 CauseOf mutants,loss
R13 T29 T28 ThemeOf tRNA aminoacylation function,loss
R14 T30 T32 CauseOf mutations,cause
R15 T30 T34 CauseOf mutations,gain-of-function
R16 T33 T30 ThemeOf CMT,mutations
R17 T33 T32 ThemeOf CMT,cause
R18 T33 T34 ThemeOf CMT,gain-of-function
R19 T36 T34 ThemeOf CMT,gain-of-function
R2 T7 T9 ThemeOf Charcot-Marie-Tooth neuropathy,caused
R3 T8 T3 ThemeOf CMT,implicated
R4 T8 T4 ThemeOf CMT,common
R5 T8 T9 ThemeOf CMT,caused
R6 T8 T10 ThemeOf CMT,mutations
R7 T10 T9 CauseOf mutations,caused
R8 T19 T10 ThemeOf CMT,mutations
R9 T19 T3 ThemeOf CMT,implicated