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PubMed:1010253 JSONTXT

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sentences

Id Subject Object Predicate Lexical cue
TextSentencer_T1 0-61 Sentence denotes [The Holt-Oram syndrome: report of a case (author's transl)].
TextSentencer_T2 62-84 Sentence denotes Sindrome di Holt-Oram.
TextSentencer_T3 85-107 Sentence denotes Descrizione di un caso
TextSentencer_T4 108-327 Sentence denotes A case of the Holt-Oram syndrome is described, that is, the association of a skeletal anomaly of the superior limbs, with a constant involvment of the thumbs, and an ostium secundum defect with a prolonged P-R interval.
TextSentencer_T5 328-495 Sentence denotes The case presented has the peculiarity of being sporadic, while from the literature a familiarity is almost constant via an autosomic dominant hereditary transmission.
TextSentencer_T6 496-636 Sentence denotes The more common syndromes were an alteration of the superior limbs is associated with a congenital cardiopathy are schematically underlined.
TextSentencer_T7 637-723 Sentence denotes Finally, the embriological reasons of this not rare association are briefly discussed.
T1 0-61 Sentence denotes [The Holt-Oram syndrome: report of a case (author's transl)].
T2 62-84 Sentence denotes Sindrome di Holt-Oram.
T3 85-107 Sentence denotes Descrizione di un caso
T4 108-327 Sentence denotes A case of the Holt-Oram syndrome is described, that is, the association of a skeletal anomaly of the superior limbs, with a constant involvment of the thumbs, and an ostium secundum defect with a prolonged P-R interval.
T5 328-495 Sentence denotes The case presented has the peculiarity of being sporadic, while from the literature a familiarity is almost constant via an autosomic dominant hereditary transmission.
T6 496-636 Sentence denotes The more common syndromes were an alteration of the superior limbs is associated with a congenital cardiopathy are schematically underlined.
T7 637-723 Sentence denotes Finally, the embriological reasons of this not rare association are briefly discussed.

performance-test

Id Subject Object Predicate Lexical cue
PD-UBERON-AE-B_T1 218-223 http://purl.obolibrary.org/obo/UBERON_0002101 denotes limbs
PD-UBERON-AE-B_T2 557-562 http://purl.obolibrary.org/obo/UBERON_0002101 denotes limbs

PubCasesORDO

Id Subject Object Predicate Lexical cue
TI1 5-23 ORDO:392 denotes Holt-Oram syndrome
AB1 122-140 ORDO:392 denotes Holt-Oram syndrome

UBERON-AE

Id Subject Object Predicate Lexical cue
PD-UBERON-AE-B_T1 218-223 http://purl.obolibrary.org/obo/UBERON_0002101 denotes limbs
PD-UBERON-AE-B_T2 557-562 http://purl.obolibrary.org/obo/UBERON_0002101 denotes limbs

PubmedHPO

Id Subject Object Predicate Lexical cue
T1 185-201 HP_0000924 denotes skeletal anomaly
T2 241-265 HP_0001172 denotes involvment of the thumbs
T3 452-470 HP_0000006 denotes autosomic dominant