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PubMed:8663148 JSONTXT 31 Projects

Annnotations TAB TSV DIC JSON TextAE Lectin_function IAV-Glycan

Id Subject Object Predicate Lexical cue
T1 12-24 protein_family_or_group denotes XPB helicase
T2 35-62 protein_family_or_group denotes repair/transcription factor
T3 63-68 protein_molecule denotes TFIIH
T4 115-125 other_name denotes DNA repair
T5 130-143 other_name denotes transcription
T6 145-148 protein_subunit denotes XPB
T7 175-195 protein_family_or_group denotes transcription factor
T8 196-201 protein_molecule denotes TFIIH
T9 347-350 protein_subunit denotes XPB
T10 407-428 other_name denotes xeroderma pigmentosum
T11 430-432 other_name denotes XP
T12 438-457 other_name denotes Cockayne's syndrome
T13 459-461 other_name denotes CS
T14 481-486 protein_molecule denotes TFIIH
T15 513-520 multi_cell denotes patient
T16 522-528 multi_cell denotes XP11BE
T17 547-566 other_name denotes frameshift mutation
T18 568-576 protein_molecule denotes TFIIHmut
T19 591-597 multi_cell denotes mother
T20 606-613 multi_cell denotes patient
T21 615-622 protein_molecule denotes TFIIHwt
T22 641-665 other_name denotes biochemical consequences
T23 721-734 other_name denotes stoichiometry
T24 738-745 protein_molecule denotes TFIIHwt
T25 747-755 protein_molecule denotes TFIIHmut
T26 782-785 protein_subunit denotes XPB
T27 832-852 protein_molecule denotes DNA-dependent ATPase
T28 911-914 protein_subunit denotes XPB
T29 928-931 protein_subunit denotes XPB
T30 950-967 other_name denotes severe NER defect
T31 1020-1048 other_name denotes basal transcription activity
T32 1192-1202 other_name denotes NER defect
T33 1262-1290 other_name denotes naturally occurring mutation
T34 1296-1301 protein_family_or_group denotes basal
T35 1302-1322 protein_family_or_group denotes transcription factor
T36 1366-1369 other_name denotes XP/
T37 1369-1371 other_name denotes CS
T38 1425-1456 other_name denotes transcription/repair deficiency