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PubMed:24227897 JSONTXT

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PubmedHPO

Id Subject Object Predicate Lexical cue
T1 112-124 HP_0000362 denotes Otosclerosis
T2 158-176 HP_0000365 denotes hearing impairment
T3 358-381 HP_0000405 denotes Conductive hearing loss
T4 369-381 HP_0000365 denotes hearing loss
T5 552-587 HP_0008625 denotes profound sensorineural hearing loss
T6 552-582 HP_0008625 denotes profound sensorineural hearing
T7 561-587 HP_0000407 denotes sensorineural hearing loss
T8 575-587 HP_0000365 denotes hearing loss
T9 606-618 HP_0000362 denotes otosclerosis
T10 804-816 HP_0000362 denotes otosclerosis
T11 1013-1025 HP_0000362 denotes otosclerosis
T12 1180-1192 HP_0000362 denotes otosclerosis
T13 1374-1386 HP_0000362 denotes otosclerosis

DisGeNET

Id Subject Object Predicate Lexical cue
T0 32-36 gene:5649 denotes RELN
T1 65-77 disease:C0029899 denotes otosclerosis
T2 811-880 gene:5649 denotes rosis. The strongest association has been demonstrated for the reelin
T3 1013-1025 disease:C0029899 denotes otosclerosis
T4 1170-1176 gene:5649 denotes reelin
T5 1180-1192 disease:C0029899 denotes otosclerosis
R1 T0 T1 associated_with RELN,otosclerosis
R2 T2 T3 associated_with rosis. The strongest association has been demonstrated for the reelin,otosclerosis
R3 T4 T5 associated_with reelin,otosclerosis