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PubMed:29959045 JSONTXT 2 Projects

Annnotations TAB TSV DIC JSON TextAE Lectin_function IAV-Glycan

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-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-2 T-14 T-22 CauseOf frameshift,diagnosed
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
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