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PubMed:10023043 JSONTXT

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bionlp-st-gro-2013-development

Id Subject Object Predicate Lexical cue
T1 25-33 Promoter denotes promoter
T2 58-63 Eukaryote denotes human
T3 64-81 Gene denotes UHS keratin genes
T5 97-102 Eukaryote denotes human
T8 142-145 ProteinSubunit denotes XPB
T9 150-153 ProteinSubunit denotes XPD
T10 159-167 ProteinSubunit denotes subunits
T13 274-279 Eukaryote denotes human
T16 449-466 Gene denotes UHS keratin genes
T18 493-503 Tissue denotes follicular
T19 508-523 Tissue denotes epidermal cells
T20 589-594 Gene denotes genes
T21 621-629 Promoter denotes promoter
T22 795-800 Gene denotes genes
T29 945-950 TranscriptionFactor denotes TFIIH
T30 951-959 ProteinSubunit denotes subunits
T11 175-208 TranscriptionFactor denotes transcription/repair factor TFIIH
T12 280-292 Protein denotes UHS proteins
T31 728-738 TATAbox denotes TATA-boxes
T32 748-766 RegulatoryDNARegion denotes regulatory regions
E1 83-86 Disease denotes TTD
E2 111-118 Disease denotes disease
E3 129-138 Mutation denotes mutations
E5 370-390 NegativeRegulationOfTranscription denotes transcription defect
E6 480-489 GeneExpression denotes expressed
E7 832-842 RegulatoryProcess denotes regulation
E8 852-865 Transcription denotes transcription
E9 883-890 RegulatoryProcess denotes control
E10 900-910 GeneExpression denotes expression
E12 932-941 Mutation denotes mutations
E4 129-138 Mutation denotes mutations
R1 T3 T2 fromSpecies UHS keratin genes,human
R4 E6 T18 locatedIn expressed,follicular
R5 E6 T19 locatedIn expressed,epidermal cells
R6 T20 T21 hasPart genes,promoter
R7 T29 T30 hasPart TFIIH,subunits
R8 E2 T5 fromSpecies disease,human
R2 T11 T10 hasPart transcription/repair factor TFIIH,subunits
R3 T12 T13 fromSpecies UHS proteins,human
R5 T8 E3 hasPatient XPB,mutations
R6 T16 E6 hasPatient UHS keratin genes,expressed
R7 E8 E7 hasPatient transcription,regulation
R8 E10 E9 hasPatient expression,control
R9 E12 E10 hasAgent mutations,expression
R10 T22 E10 hasPatient genes,expression
R11 T30 E12 hasPatient subunits,mutations
R12 T9 E4 hasPatient XPD,mutations

PubmedHPO

Id Subject Object Predicate Lexical cue
T1 323-335 HP_0002299 denotes brittle hair

DisGeNET

Id Subject Object Predicate Lexical cue
T0 83-86 gene:2068 denotes TTD
T1 103-118 disease:C0019247 denotes genetic disease
T2 83-86 gene:404672 denotes TTD
T3 103-118 disease:C0019247 denotes genetic disease
T4 203-208 gene:2965 denotes TFIIH
T5 323-335 disease:C0263490 denotes brittle hair
T6 203-208 gene:730394 denotes TFIIH
T7 323-335 disease:C0263490 denotes brittle hair
T8 203-208 gene:2967 denotes TFIIH
T9 323-335 disease:C0263490 denotes brittle hair
T10 203-208 gene:2966 denotes TFIIH
T11 323-335 disease:C0263490 denotes brittle hair
T12 203-208 gene:2968 denotes TFIIH
T13 323-335 disease:C0263490 denotes brittle hair
T14 203-208 gene:2068 denotes TFIIH
T15 323-335 disease:C0263490 denotes brittle hair
T16 203-208 gene:2071 denotes TFIIH
T17 323-335 disease:C0263490 denotes brittle hair
T18 203-208 gene:404672 denotes TFIIH
T19 323-335 disease:C0263490 denotes brittle hair
T20 203-208 gene:728340 denotes TFIIH
T21 323-335 disease:C0263490 denotes brittle hair
R1 T0 T1 associated_with TTD,genetic disease
R2 T2 T3 associated_with TTD,genetic disease
R3 T4 T5 associated_with TFIIH,brittle hair
R4 T6 T7 associated_with TFIIH,brittle hair
R5 T8 T9 associated_with TFIIH,brittle hair
R6 T10 T11 associated_with TFIIH,brittle hair
R7 T12 T13 associated_with TFIIH,brittle hair
R8 T14 T15 associated_with TFIIH,brittle hair
R9 T16 T17 associated_with TFIIH,brittle hair
R10 T18 T19 associated_with TFIIH,brittle hair
R11 T20 T21 associated_with TFIIH,brittle hair

DisGeNET5_gene_disease

Id Subject Object Predicate Lexical cue
10023043-1#0#3#gene2068 83-86 gene2068 denotes TTD
10023043-1#120#125#gene2068 203-208 gene2068 denotes TFIIH
10023043-1#120#125#gene2071 203-208 gene2071 denotes TFIIH
10023043-1#59#62#gene2071 142-145 gene2071 denotes XPB
10023043-1#67#70#gene2068 150-153 gene2068 denotes XPD
10023043-1#240#252#diseaseC0263490 323-335 diseaseC0263490 denotes brittle hair
0#3#gene2068240#252#diseaseC0263490 10023043-1#0#3#gene2068 10023043-1#240#252#diseaseC0263490 associated_with TTD,brittle hair
120#125#gene2068240#252#diseaseC0263490 10023043-1#120#125#gene2068 10023043-1#240#252#diseaseC0263490 associated_with TFIIH,brittle hair
120#125#gene2071240#252#diseaseC0263490 10023043-1#120#125#gene2071 10023043-1#240#252#diseaseC0263490 associated_with TFIIH,brittle hair
59#62#gene2071240#252#diseaseC0263490 10023043-1#59#62#gene2071 10023043-1#240#252#diseaseC0263490 associated_with XPB,brittle hair
67#70#gene2068240#252#diseaseC0263490 10023043-1#67#70#gene2068 10023043-1#240#252#diseaseC0263490 associated_with XPD,brittle hair