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PubMed:10767339 JSONTXT

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PubmedHPO

Id Subject Object Predicate Lexical cue
T1 132-150 HP_0001249 denotes mental retardation
T2 375-389 HP_0000053 denotes macroorchidism
T3 394-418 HP_0000708 denotes behavioral abnormalities
T4 1489-1496 HP_0000739 denotes anxiety
T5 1667-1685 HP_0000708 denotes abnormal behaviors

DisGeNET5_gene_disease

Id Subject Object Predicate Lexical cue
10767339-1#95#99#gene2332 187-191 gene2332 denotes FMR1
10767339-1#40#58#diseaseC0025362 132-150 diseaseC0025362 denotes mental retardation
10767339-1#40#58#diseaseC3714756 132-150 diseaseC3714756 denotes mental retardation
10767339-3#0#4#gene2332 294-298 gene2332 denotes Fmr1
10767339-3#81#95#diseaseC1263023 375-389 diseaseC1263023 denotes macroorchidism
10767339-3#100#124#diseaseC0233514 394-418 diseaseC0233514 denotes behavioral abnormalities
10767339-4#47#51#gene2332 467-471 gene2332 denotes FMR1
10767339-4#240#244#gene2332 660-664 gene2332 denotes Fmr1
10767339-4#121#139#diseaseC0016667 541-559 diseaseC0016667 denotes fragile X syndrome
95#99#gene233240#58#diseaseC0025362 10767339-1#95#99#gene2332 10767339-1#40#58#diseaseC0025362 associated_with FMR1,mental retardation
95#99#gene233240#58#diseaseC3714756 10767339-1#95#99#gene2332 10767339-1#40#58#diseaseC3714756 associated_with FMR1,mental retardation
0#4#gene233281#95#diseaseC1263023 10767339-3#0#4#gene2332 10767339-3#81#95#diseaseC1263023 associated_with Fmr1,macroorchidism
0#4#gene2332100#124#diseaseC0233514 10767339-3#0#4#gene2332 10767339-3#100#124#diseaseC0233514 associated_with Fmr1,behavioral abnormalities
47#51#gene2332121#139#diseaseC0016667 10767339-4#47#51#gene2332 10767339-4#121#139#diseaseC0016667 associated_with FMR1,fragile X syndrome
240#244#gene2332121#139#diseaseC0016667 10767339-4#240#244#gene2332 10767339-4#121#139#diseaseC0016667 associated_with Fmr1,fragile X syndrome

NCBIDiseaseCorpus

Id Subject Object Predicate Lexical cue
T1 20-35 SpecificDisease:OMIM:300624 denotes FMR1 deficiency
T2 92-110 SpecificDisease:D005600 denotes Fragile X syndrome
T3 132-150 DiseaseClass:D008607 denotes mental retardation
T4 375-389 SpecificDisease:D005600 denotes macroorchidism
T5 541-559 SpecificDisease:D005600 denotes fragile X syndrome
T6 1203-1212 Modifier:D005600 denotes fragile X
T7 1489-1496 Modifier:D001008 denotes anxiety
T8 1772-1790 SpecificDisease:D005600 denotes fragile X syndrome

DisGeNET

Id Subject Object Predicate Lexical cue
T0 187-191 gene:2332 denotes FMR1
T1 132-150 disease:C0025362 denotes mental retardation
T2 187-191 gene:2477 denotes FMR1
T3 132-150 disease:C0025362 denotes mental retardation
T4 187-191 gene:2477 denotes FMR1
T5 92-110 disease:C0016667 denotes Fragile X syndrome
T6 187-191 gene:2332 denotes FMR1
T7 92-110 disease:C0016667 denotes Fragile X syndrome
T8 294-298 gene:2332 denotes Fmr1
T9 375-389 disease:C1263023 denotes macroorchidism
T10 294-298 gene:2477 denotes Fmr1
T11 375-389 disease:C1263023 denotes macroorchidism
R1 T0 T1 associated_with FMR1,mental retardation
R2 T2 T3 associated_with FMR1,mental retardation
R3 T4 T5 associated_with FMR1,Fragile X syndrome
R4 T6 T7 associated_with FMR1,Fragile X syndrome
R5 T8 T9 associated_with Fmr1,macroorchidism
R6 T10 T11 associated_with Fmr1,macroorchidism

NCBI-Disease-Train

Id Subject Object Predicate Lexical cue database_id
T193 20-35 SpecificDisease denotes FMR1 deficiency OMIM:300624
T194 92-110 SpecificDisease denotes Fragile X syndrome D005600
T195 132-150 DiseaseClass denotes mental retardation D008607
T196 375-389 SpecificDisease denotes macroorchidism D005600
T197 541-559 SpecificDisease denotes fragile X syndrome D005600
T198 1203-1212 Modifier denotes fragile X D005600
T199 1489-1496 Modifier denotes anxiety D001008
T200 1772-1790 SpecificDisease denotes fragile X syndrome D005600

NCBI-Disease-Corpus-All

Id Subject Object Predicate Lexical cue database_id
T193 20-35 SpecificDisease denotes FMR1 deficiency OMIM:300624
T194 92-110 SpecificDisease denotes Fragile X syndrome D005600
T195 132-150 DiseaseClass denotes mental retardation D008607
T196 375-389 SpecificDisease denotes macroorchidism D005600
T197 541-559 SpecificDisease denotes fragile X syndrome D005600
T198 1203-1212 Modifier denotes fragile X D005600
T199 1489-1496 Modifier denotes anxiety D001008
T200 1772-1790 SpecificDisease denotes fragile X syndrome D005600

NCBI-Disease-Corpus-2stage-All

Id Subject Object Predicate Lexical cue
T1 92-110 SpecificDisease denotes Fragile X syndrome
T2 375-389 SpecificDisease denotes macroorchidism
T3 541-559 SpecificDisease denotes fragile X syndrome
T4 1039-1054 SpecificDisease denotes Macro-orchidism
T5 1203-1212 SpecificDisease denotes fragile X
T6 1772-1790 SpecificDisease denotes fragile X syndrome

NCBI-Disease-Corpus-rezarta-All

Id Subject Object Predicate Lexical cue
T1 92-110 SpecificDisease denotes Fragile X syndrome
T2 541-559 SpecificDisease denotes fragile X syndrome
T3 1203-1212 SpecificDisease denotes fragile X
T4 1772-1790 SpecificDisease denotes fragile X syndrome

NCBI-Disease-Corpus-4oGuideline-All

Id Subject Object Predicate Lexical cue
T1 92-110 SpecificDisease denotes Fragile X syndrome
T2 132-150 DiseaseClass denotes mental retardation
T3 375-389 SpecificDisease denotes macroorchidism
T4 541-559 SpecificDisease denotes fragile X syndrome
T5 1039-1054 SpecificDisease denotes Macro-orchidism
T6 1203-1212 Modifier denotes fragile X
T7 1772-1790 SpecificDisease denotes fragile X syndrome