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PubMed:6964893 JSONTXT

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DisGeNET

Id Subject Object Predicate Lexical cue
T0 1275-1278 gene:55143 denotes BOR
T1 1293-1308 disease:C0235831 denotes renal dysplasia
T2 1275-1278 gene:55143 denotes BOR
T3 1293-1308 disease:C3536714 denotes renal dysplasia
T4 1275-1278 gene:2138 denotes BOR
T5 1293-1308 disease:C0235831 denotes renal dysplasia
T6 1275-1278 gene:2138 denotes BOR
T7 1293-1308 disease:C3536714 denotes renal dysplasia
R1 T0 T1 associated_with BOR,renal dysplasia
R2 T2 T3 associated_with BOR,renal dysplasia
R3 T4 T5 associated_with BOR,renal dysplasia
R4 T6 T7 associated_with BOR,renal dysplasia

BioLarkPubmedHPO

Id Subject Object Predicate Lexical cue
HP:0004467 104-111 HP:0004467 denotes earpits
HP:0000404 112-120 HP:0000404 denotes deafness
HP:0004467 496-503 HP:0004467 denotes earpits
HP:0000404 504-512 HP:0000404 denotes deafness
HP:0000006 528-546 HP:0000006 denotes autosomal dominant
HP:0000407 595-642 HP:0000407 denotes sensorineural, conductive or mixed hearing loss
HP:0000405 610-642 HP:0000405 denotes conductive or mixed hearing loss
HP:0000410 624-642 HP:0000410 denotes mixed hearing loss
HP:0004467 644-661 HP:0004467 denotes preauricular pits
HP:0000356 674-716 HP:0000356 denotes defects of the outer, middle and inner ear
HP:0000370 674-716 HP:0000370 denotes defects of the outer, middle and inner ear
HP:0000359 674-716 HP:0000359 denotes defects of the outer, middle and inner ear
HP:0007925 718-740 HP:0007925 denotes lacrimal duct stenosis
HP:0009795 742-760 HP:0009795 denotes branchial fistulas
HP:0009796 742-769 HP:0009796 denotes branchial fistulas or cysts
HP:0000077 804-819 HP:0000077 denotes renal anomalies
HP:0004467 950-954 HP:0004467 denotes Pits
HP:0009794 956-972 HP:0009794 denotes branchial clefts
HP:0000365 977-989 HP:0000365 denotes hearing loss
HP:0000792 1033-1051 HP:0000792 denotes renal malformation
HP:0000365 1505-1517 HP:0000365 denotes hearing loss
T1 104-111 HP:0004467 denotes earpits
T2 112-120 HP:0000404 denotes deafness
T3 496-503 HP:0004467 denotes earpits
T4 504-512 HP:0000404 denotes deafness
T5 528-546 HP:0000006 denotes autosomal dominant
T6 595-642 HP:0000407 denotes sensorineural, conductive or mixed hearing loss
T7 610-642 HP:0000405 denotes conductive or mixed hearing loss
T8 624-642 HP:0000410 denotes mixed hearing loss
T9 644-661 HP:0004467 denotes preauricular pits
T10 674-716 HP:0000356 denotes defects of the outer, middle and inner ear
T11 674-716 HP:0000370 denotes defects of the outer, middle and inner ear
T12 674-716 HP:0000359 denotes defects of the outer, middle and inner ear
T13 718-740 HP:0007925 denotes lacrimal duct stenosis
T14 742-760 HP:0009795 denotes branchial fistulas
T15 742-769 HP:0009796 denotes branchial fistulas or cysts
T16 804-819 HP:0000077 denotes renal anomalies
T17 950-954 HP:0004467 denotes Pits
T18 956-972 HP:0009794 denotes branchial clefts
T19 977-989 HP:0000365 denotes hearing loss
T20 1033-1051 HP:0000792 denotes renal malformation
T21 1505-1517 HP:0000365 denotes hearing loss
T1 104-111 HP:0004467 denotes earpits
T2 112-120 HP:0000404 denotes deafness
T3 496-503 HP:0004467 denotes earpits
T4 504-512 HP:0000404 denotes deafness
T5 528-546 HP:0000006 denotes autosomal dominant
T6 595-642 HP:0000407 denotes sensorineural, conductive or mixed hearing loss
T7 610-642 HP:0000405 denotes conductive or mixed hearing loss
T8 624-642 HP:0000410 denotes mixed hearing loss
T9 644-661 HP:0004467 denotes preauricular pits
T10 674-716 HP:0000356 denotes defects of the outer, middle and inner ear
T11 674-716 HP:0000370 denotes defects of the outer, middle and inner ear
T12 674-716 HP:0000359 denotes defects of the outer, middle and inner ear
T13 718-740 HP:0007925 denotes lacrimal duct stenosis
T14 742-760 HP:0009795 denotes branchial fistulas
T15 742-769 HP:0009796 denotes branchial fistulas or cysts
T16 804-819 HP:0000077 denotes renal anomalies
T17 950-954 HP:0004467 denotes Pits
T18 956-972 HP:0009794 denotes branchial clefts
T19 977-989 HP:0000365 denotes hearing loss
T20 1033-1051 HP:0000792 denotes renal malformation
T21 1505-1517 HP:0000365 denotes hearing loss
T1 104-111 HP:0004467 denotes earpits
T2 112-120 HP:0000404 denotes deafness
T3 496-503 HP:0004467 denotes earpits
T4 504-512 HP:0000404 denotes deafness
T5 528-546 HP:0000006 denotes autosomal dominant
T6 595-642 HP:0000407 denotes sensorineural, conductive or mixed hearing loss
T7 610-642 HP:0000405 denotes conductive or mixed hearing loss
T8 624-642 HP:0000410 denotes mixed hearing loss
T9 644-661 HP:0004467 denotes preauricular pits
T10 674-716 HP:0000356 denotes defects of the outer, middle and inner ear
T11 674-716 HP:0000370 denotes defects of the outer, middle and inner ear
T12 674-716 HP:0000359 denotes defects of the outer, middle and inner ear
T13 718-740 HP:0007925 denotes lacrimal duct stenosis
T14 742-760 HP:0009795 denotes branchial fistulas
T15 742-769 HP:0009796 denotes branchial fistulas or cysts
T16 804-819 HP:0000077 denotes renal anomalies
T17 950-954 HP:0004467 denotes Pits
T18 956-972 HP:0009794 denotes branchial clefts
T19 977-989 HP:0000365 denotes hearing loss
T20 1033-1051 HP:0000792 denotes renal malformation
T21 1505-1517 HP:0000365 denotes hearing loss