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sonoma

Id Subject Object Predicate Lexical cue
T-0 3-41 DISEASE denotes MED13L-related intellectual disability
T-1 81-95 GENE denotes MED13L-related
T-2 123-136 REG denotes characterized
T-3 149-172 DISEASE denotes intellectual disability
T-4 174-176 DISEASE denotes ID
T-5 179-196 DISEASE denotes speech impairment
T-6 202-228 DISEASE denotes dysmorphic facial features
T-7 257-295 DISEASE denotes MED13L-related intellectual disability
T-8 434-453 VAR denotes genetic aberrations
T-9 474-476 DISEASE denotes ID
T-10 617-655 DISEASE denotes MED13L-related intellectual disability
T-11 761-767 GENE denotes MED13L
T-12 768-779 VAR denotes aberrations
T-13 806-820 VAR denotes microdeletions
T-14 826-836 VAR denotes frameshift
T-15 844-861 VAR denotes nonsense variants
T-16 871-887 VAR denotes missense variant
T-17 914-917 REG denotes had
T-18 918-941 DISEASE denotes intellectual disability
T-19 943-965 DISEASE denotes speech and motor delay
T-20 1017-1029 DISEASE denotes macroglossia
T-21 1038-1049 DISEASE denotes macrostomia
T-22 1073-1082 REG denotes diagnosed
T-23 1088-1094 DISEASE denotes autism
T-24 1108-1125 DISEASE denotes autistic features
T-25 1135-1166 DISEASE denotes complex congenital heart defect
T-26 1191-1204 DISEASE denotes foramen ovale
T-27 1288-1307 DISEASE denotes genetic aberrations
T-28 1356-1394 DISEASE denotes MED13L-related intellectual disability
T-29 1424-1432 DISEASE denotes syndrome
T-30 1498-1517 DISEASE denotes developmental delay
T-31 1519-1536 DISEASE denotes speech impairment
T-32 1538-1555 DISEASE denotes bulbous nasal tip
T-33 1561-1573 DISEASE denotes macroglossia
T-34 1575-1586 DISEASE denotes macrostomia
R-0 T-5 T-2 ThemeOf speech impairment,characterized
R-1 T-14 T-17 CauseOf frameshift,had
R-2 T-14 T-22 CauseOf frameshift,diagnosed
R-3 T-30 T-28 ThemeOf developmental delay,MED13L-related intellectual disability
R-4 T-32 T-28 ThemeOf bulbous nasal tip,MED13L-related intellectual disability
R-5 T-11 T-13 ThemeOf MED13L,microdeletions
R-6 T-11 T-14 ThemeOf MED13L,frameshift
R-7 T-11 T-12 ThemeOf MED13L,aberrations
R-8 T-11 T-15 ThemeOf MED13L,nonsense variants
R-9 T-34 T-28 ThemeOf macrostomia,MED13L-related intellectual disability
R-10 T-33 T-28 ThemeOf macroglossia,MED13L-related intellectual disability
R-11 T-4 T-2 ThemeOf ID,characterized
R-12 T-8 T-9 ThemeOf genetic aberrations,ID
R-13 T-8 T-10 ThemeOf genetic aberrations,MED13L-related intellectual disability
R-14 T-18 T-17 ThemeOf intellectual disability,had
R-15 T-21 T-17 ThemeOf macrostomia,had
R-16 T-19 T-17 ThemeOf speech and motor delay,had
R-17 T-12 T-17 CauseOf aberrations,had
R-18 T-13 T-22 CauseOf microdeletions,diagnosed
R-19 T-13 T-17 CauseOf microdeletions,had
R-20 T-15 T-22 CauseOf nonsense variants,diagnosed
R-21 T-15 T-17 CauseOf nonsense variants,had
R-22 T-16 T-22 CauseOf missense variant,diagnosed
R-23 T-16 T-17 CauseOf missense variant,had
R-24 T-3 T-2 ThemeOf intellectual disability,characterized
R-25 T-20 T-17 ThemeOf macroglossia,had
R-26 T-31 T-28 ThemeOf speech impairment,MED13L-related intellectual disability
R-27 T-1 T-2 ThemeOf MED13L-related,characterized

sonoma2

Id Subject Object Predicate Lexical cue
T0 3-41 DISEASE denotes MED13L-related intellectual disability
T1 3-17 GENE denotes MED13L-related
T2 80-94 GENE denotes MED13L-relate
T3 81-119 DISEASE denotes MED13L-related intellectual disability
T4 123-136 REG denotes characterized
T5 149-172 CPA denotes intellectual disability
T6 174-176 CPA denotes ID
T7 178-195 DISEASE denotes speech impairmen
T8 186-196 CPA denotes impairment
T9 201-218 DISEASE denotes dysmorphic facia
T10 202-212 DISEASE denotes dysmorphic
T11 213-228 CPA denotes facial features
T12 256-270 GENE denotes MED13L-relate
T13 257-295 DISEASE denotes MED13L-related intellectual disability
T14 432-451 DISEASE denotes r genetic aberratio
T15 442-453 VAR denotes aberrations
T16 474-476 CPA denotes ID
T17 615-629 GENE denotes f MED13L-relat
T18 617-655 DISEASE denotes MED13L-related intellectual disability
T19 758-764 GENE denotes vo MED
T20 761-767 GENE denotes MED13L
T21 768-779 VAR denotes aberrations
T22 806-820 VAR denotes microdeletions
T23 826-836 VAR denotes frameshift
T24 844-861 VAR denotes nonsense variants
T25 871-887 VAR denotes missense variant
T26 914-917 REG denotes had
T27 918-930 CPA denotes intellectual
T28 931-941 CPA denotes disability
T29 960-965 CPA denotes delay
T30 971-979 CPA denotes features
T31 987-992 CPA denotes mouth
T32 991-1001 DISEASE denotes h (open mo
T33 999-1015 CPA denotes mouth appearance
T34 1014-1026 DISEASE denotes e, macroglos
T35 1017-1029 DISEASE denotes macroglossia
T36 1035-1046 DISEASE denotes or macrosto
T37 1038-1049 DISEASE denotes macrostomia
T38 1073-1082 REG denotes diagnosed
T39 1085-1091 DISEASE denotes th aut
T40 1088-1094 DISEASE denotes autism
T41 1104-1107 REG denotes had
T42 1105-1113 DISEASE denotes ad autis
T43 1108-1125 CPA denotes autistic features
T44 1131-1134 REG denotes had
T45 1135-1166 DISEASE denotes complex congenital heart defect
T46 1140-1163 DISEASE denotes ex congenital heart def
T47 1176-1179 REG denotes had
T48 1191-1204 CPA denotes foramen ovale
T49 1285-1304 DISEASE denotes nd genetic aberrati
T50 1296-1307 VAR denotes aberrations
T51 1352-1366 GENE denotes of MED13L-rel
T52 1356-1394 DISEASE denotes MED13L-related intellectual disability
T53 1424-1432 CPA denotes syndrome
T54 1483-1494 REG denotes association
T55 1498-1511 CPA denotes developmental
T56 1512-1517 CPA denotes delay
T57 1515-1551 DISEASE denotes ay, speech impairment, bulbous nasal
T58 1519-1525 CPA denotes speech
T59 1526-1536 CPA denotes impairment
T60 1538-1555 CPA denotes bulbous nasal tip
T61 1557-1569 DISEASE denotes and macroglo
T62 1561-1573 DISEASE denotes macroglossia
T63 1571-1582 DISEASE denotes ia, macrost
T64 1575-1586 DISEASE denotes macrostomia
T65 1587-1597 DISEASE denotes or open m
T66 1596-1612 CPA denotes mouth appearance
R2 T5 T4 ThemeOf intellectual disability,characterized
R3 T6 T4 ThemeOf ID,characterized
R4 T8 T4 ThemeOf impairment,characterized
R5 T10 T4 ThemeOf dysmorphic,characterized
R6 T10 T11 ThemeOf dysmorphic,facial features
R7 T11 T4 ThemeOf facial features,characterized
R8 T16 T15 ThemeOf ID,aberrations
R9 T20 T21 ThemeOf MED13L,aberrations
R10 T20 T22 ThemeOf MED13L,microdeletions
R11 T20 T23 ThemeOf MED13L,frameshift
R12 T20 T24 ThemeOf MED13L,nonsense variants
R13 T20 T25 ThemeOf MED13L,missense variant
R0 T0 T4 ThemeOf MED13L-related intellectual disability,characterized
R1 T3 T4 ThemeOf MED13L-related intellectual disability,characterized
R14 T22 T21 ThemeOf microdeletions,aberrations
R15 T21 T26 CauseOf aberrations,had
R16 T22 T26 CauseOf microdeletions,had
R17 T23 T21 ThemeOf frameshift,aberrations
R18 T23 T26 CauseOf frameshift,had
R19 T24 T21 ThemeOf nonsense variants,aberrations
R20 T24 T26 CauseOf nonsense variants,had
R21 T25 T21 ThemeOf missense variant,aberrations
R22 T25 T26 CauseOf missense variant,had
R23 T27 T26 ThemeOf intellectual,had
R24 T27 T28 ThemeOf intellectual,disability
R25 T27 T30 ThemeOf intellectual,features
R26 T28 T26 ThemeOf disability,had
R27 T28 T30 ThemeOf disability,features
R28 T29 T26 ThemeOf delay,had
R29 T30 T26 ThemeOf features,had
R30 T31 T30 ThemeOf mouth,features
R31 T31 T26 ThemeOf mouth,had
R32 T33 T26 ThemeOf mouth appearance,had
R33 T33 T30 ThemeOf mouth appearance,features
R34 T33 T31 ThemeOf mouth appearance,mouth
R35 T35 T26 ThemeOf macroglossia,had
R36 T35 T30 ThemeOf macroglossia,features
R37 T37 T26 ThemeOf macrostomia,had
R38 T37 T30 ThemeOf macrostomia,features
R39 T40 T38 ThemeOf autism,diagnosed
R40 T40 T41 ThemeOf autism,had
R41 T40 T44 ThemeOf autism,had
R42 T40 T47 ThemeOf autism,had
R43 T43 T38 ThemeOf autistic features,diagnosed
R44 T43 T41 ThemeOf autistic features,had
R45 T43 T44 ThemeOf autistic features,had
R46 T45 T38 ThemeOf complex congenital heart defect,diagnosed
R47 T45 T41 ThemeOf complex congenital heart defect,had
R48 T45 T44 ThemeOf complex congenital heart defect,had
R49 T45 T47 ThemeOf complex congenital heart defect,had
R50 T48 T38 ThemeOf foramen ovale,diagnosed
R51 T48 T47 ThemeOf foramen ovale,had
R52 T52 T53 ThemeOf MED13L-related intellectual disability,syndrome
R53 T52 T54 ThemeOf MED13L-related intellectual disability,association
R54 T53 T54 ThemeOf syndrome,association
R55 T55 T54 ThemeOf developmental,association
R56 T56 T54 ThemeOf delay,association
R57 T58 T54 ThemeOf speech,association
R58 T59 T54 ThemeOf impairment,association
R59 T60 T54 ThemeOf bulbous nasal tip,association
R60 T62 T54 ThemeOf macroglossia,association
R61 T64 T54 ThemeOf macrostomia,association
R62 T66 T54 ThemeOf mouth appearance,association