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NCBIDiseaseCorpus

Id Subject Object Predicate Lexical cue
T1 19-32 SpecificDisease:OMIM:610102 denotes C7 deficiency
T2 82-95 SpecificDisease:OMIM:610102 denotes C7 deficiency
T3 646-658 Modifier:OMIM:610102 denotes C7-deficient

ncbi-valid

Id Subject Object Predicate Lexical cue
T1 19-32 SpecificDisease denotes C7 deficiency
T2 82-95 SpecificDisease denotes C7 deficiency
T3 646-658 Modifier denotes C7-deficient

ncbi-valid-gpt-nr-ng

Id Subject Object Predicate Lexical cue
T1 19-32 SpecificDisease denotes C7 deficiency
T2 82-95 SpecificDisease denotes C7 deficiency
T3 646-658 SpecificDisease denotes C7-deficient

ncbi-valid-gpt-nr-g

Id Subject Object Predicate Lexical cue
T1 19-32 SpecificDisease denotes C7 deficiency
T2 82-95 SpecificDisease denotes C7 deficiency
T3 646-658 Modifier denotes C7-deficient

ncbi-valid-gpt-r-g

Id Subject Object Predicate Lexical cue
T1 19-32 SpecificDisease denotes C7 deficiency
T2 82-95 SpecificDisease denotes C7 deficiency
T3 646-658 Modifier denotes C7-deficient

ncbi-valid-gpt-r-ng

Id Subject Object Predicate Lexical cue
T1 19-32 SpecificDisease denotes C7 deficiency
T2 82-95 SpecificDisease denotes C7 deficiency
T3 646-658 SpecificDisease denotes C7-deficient

ncbi-valid-gemini-r-g

Id Subject Object Predicate Lexical cue
T1 19-32 SpecificDisease denotes C7 deficiency
T2 646-658 Modifier denotes C7-deficient

ncbi-valid-gemini-nr-ng

Id Subject Object Predicate Lexical cue
T1 19-32 SpecificDisease denotes C7 deficiency
T2 82-95 SpecificDisease denotes C7 deficiency

ncbi-valid-gemini-nr-g

Id Subject Object Predicate Lexical cue
T1 19-32 SpecificDisease denotes C7 deficiency
T2 82-95 SpecificDisease denotes C7 deficiency

ncbi-valid-deepseek-nr-ng

Id Subject Object Predicate Lexical cue
T1 19-32 SpecificDisease denotes C7 deficiency
T2 82-95 SpecificDisease denotes C7 deficiency
T3 646-658 SpecificDisease denotes C7-deficient

ncbi-valid-deepseek-nr-g

Id Subject Object Predicate Lexical cue
T1 19-32 SpecificDisease denotes C7 deficiency
T2 82-95 SpecificDisease denotes C7 deficiency
T3 646-658 Modifier denotes C7-deficient

ncbi-valid-deepseek-r-g

Id Subject Object Predicate Lexical cue
T1 19-32 SpecificDisease denotes C7 deficiency
T2 82-95 SpecificDisease denotes C7 deficiency
T3 646-658 Modifier denotes C7-deficient

ncbi-valid-deepseek-r-ng

Id Subject Object Predicate Lexical cue
T1 19-32 SpecificDisease denotes C7 deficiency
T2 82-95 SpecificDisease denotes C7 deficiency
T3 646-658 SpecificDisease denotes C7-deficient

ncbi-valid-gemini-r-ng

Id Subject Object Predicate Lexical cue
T1 19-32 SpecificDisease denotes C7 deficiency
T2 245-257 Modifier denotes heterozygous
T3 258-272 SpecificDisease denotes point mutation
T4 422-429 SpecificDisease denotes deleted
T5 540-553 SpecificDisease denotes splice defect
T6 577-585 SpecificDisease denotes deletion
T7 646-658 Modifier denotes C7-deficient
T8 698-708 Modifier denotes homozygous
T9 715-733 SpecificDisease denotes mis-sense mutation
T10 772-784 Modifier denotes heterozygous
T11 898-917 DiseaseClass denotes deficiency mutation

ncbi-valid-gemini-r-m

Id Subject Object Predicate Lexical cue
T1 19-32 SpecificDisease denotes C7 deficiency
T2 646-658 Modifier denotes C7-deficient

ncbi-valid-gpt-r-m

Id Subject Object Predicate Lexical cue
T1 19-32 SpecificDisease denotes C7 deficiency
T2 82-95 SpecificDisease denotes C7 deficiency
T3 646-658 Modifier denotes C7-deficient

ncbi-valid-deepseek-r-m

Id Subject Object Predicate Lexical cue
T1 19-32 SpecificDisease denotes C7 deficiency
T2 82-95 SpecificDisease denotes C7 deficiency
T3 646-658 Modifier denotes C7-deficient

NCBI-Disease-Develop

Id Subject Object Predicate Lexical cue database_id
T91 19-32 SpecificDisease denotes C7 deficiency OMIM:610102
T92 82-95 SpecificDisease denotes C7 deficiency OMIM:610102
T93 646-658 Modifier denotes C7-deficient OMIM:610102

NCBI-Disease-Corpus-All

Id Subject Object Predicate Lexical cue database_id
T91 19-32 SpecificDisease denotes C7 deficiency OMIM:610102
T92 82-95 SpecificDisease denotes C7 deficiency OMIM:610102
T93 646-658 Modifier denotes C7-deficient OMIM:610102

NCBI-Disease-Corpus-2stage-All

Id Subject Object Predicate Lexical cue
T1 19-32 SpecificDisease denotes C7 deficiency
T2 82-95 SpecificDisease denotes C7 deficiency
T3 463-465 Modifier denotes C6
T4 470-472 Modifier denotes C7
T5 646-658 Modifier denotes C7-deficient
T6 677-679 Modifier denotes C7
T7 809-811 Modifier denotes C6

NCBI-Disease-Corpus-rezarta-All

Id Subject Object Predicate Lexical cue
T1 19-32 SpecificDisease denotes C7 deficiency
T2 82-95 SpecificDisease denotes C7 deficiency
T3 463-465 SpecificDisease denotes C6
T4 470-484 Modifier denotes C7 gene region
T5 646-658 Modifier denotes C7-deficient
T6 677-689 SpecificDisease denotes C7 haplotype
T7 809-816 Modifier denotes C6 loci

NCBI-Disease-Corpus-4oGuideline-All

Id Subject Object Predicate Lexical cue
T1 19-32 SpecificDisease denotes C7 deficiency
T2 82-95 SpecificDisease denotes C7 deficiency
T3 646-658 SpecificDisease denotes C7-deficient

NCBI-Disease-Corpus-Simple-All

Id Subject Object Predicate Lexical cue
T1 19-32 SpecificDisease denotes C7 deficiency
T2 82-95 SpecificDisease denotes C7 deficiency
T3 646-658 SpecificDisease denotes C7-deficient
T4 898-908 SpecificDisease denotes deficiency