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PubMed:17543510 JSONTXT

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PubmedHPO

Id Subject Object Predicate Lexical cue
T1 193-217 HP_0008660 denotes Renal tubular dysgenesis
T2 245-256 HP_0000112 denotes nephropathy
T3 291-297 HP_0100519 denotes anuria
T4 309-324 HP_0001562 denotes oligohydramnios
T5 562-577 HP_0001562 denotes oligohydramnios
T6 616-641 HP_0001518 denotes small for gestational age
T7 747-753 HP_0100519 denotes anuria

PubCasesHPO

Id Subject Object Predicate Lexical cue
AB1 245-256 HP:0000112 denotes nephropathy
AB2 291-297 HP:0100519 denotes anuria
AB3 309-324 HP:0001562 denotes oligohydramnios
AB4 562-577 HP:0001562 denotes oligohydramnios
AB5 616-641 HP:0001518 denotes small for gestational age
AB6 747-753 HP:0100519 denotes anuria

UBERON-AE

Id Subject Object Predicate Lexical cue
PD-UBERON-AE_T1 448-464 http://purl.obolibrary.org/obo/UBERON_0004134 denotes proximal tubules
PD-UBERON-AE_T2 841-856 http://purl.obolibrary.org/obo/UBERON_0004134 denotes proximal tubule
PD-UBERON-AE_T3 1074-1080 http://purl.obolibrary.org/obo/UBERON_0002113 denotes kidney

PubCasesORDO

Id Subject Object Predicate Lexical cue
AB1 193-217 ORDO:3033 denotes Renal tubular dysgenesis
TI1 21-45 ORDO:3033 denotes renal tubular dysgenesis

sentences

Id Subject Object Predicate Lexical cue
TextSentencer_T1 0-89 Sentence denotes [Autosomal recessive renal tubular dysgenesis: morphologic and genetic study of 2 cases].
TextSentencer_T2 90-192 Sentence denotes Dysgénésie tubulaire rénale autosomique récessive: étude morphologique et génétique de 2 nouveaux cas.
TextSentencer_T3 193-371 Sentence denotes Renal tubular dysgenesis (RTD) is a rare and severe nephropathy characterized by persistent fetal anuria leading to oligohydramnios with the Potter sequence, and perinatal death.
TextSentencer_T4 372-465 Sentence denotes The diagnosis is based on the histological finding of absence or paucity of proximal tubules.
TextSentencer_T5 466-601 Sentence denotes A consanguineous family is described in which 2 siblings, born after pregnancies complicated by oligohydramnios were affected with RTD.
TextSentencer_T6 602-651 Sentence denotes Patients were small for gestational age at birth.
TextSentencer_T7 652-780 Sentence denotes The first patient died after a few hours, the second after a few days of life, with persistent anuria unresponsive to treatment.
TextSentencer_T8 781-916 Sentence denotes Histologically, there was marked reduction in the number of proximal tubule sections and no renin was detected by immunohistochemistry.
TextSentencer_T9 917-999 Sentence denotes An homozygous mutation of the gene encoding renin was identified in both patients.
TextSentencer_T10 1000-1246 Sentence denotes This study underlines the interest of the histological examination of the kidney for the diagnostic of RTD in anuric fetuses and newborns, and the possibility of mutation analysis of RAS genes for genetic counselling and early prenatal diagnosis.
T1 0-89 Sentence denotes [Autosomal recessive renal tubular dysgenesis: morphologic and genetic study of 2 cases].
T2 90-192 Sentence denotes Dysgénésie tubulaire rénale autosomique récessive: étude morphologique et génétique de 2 nouveaux cas.
T3 193-371 Sentence denotes Renal tubular dysgenesis (RTD) is a rare and severe nephropathy characterized by persistent fetal anuria leading to oligohydramnios with the Potter sequence, and perinatal death.
T4 372-465 Sentence denotes The diagnosis is based on the histological finding of absence or paucity of proximal tubules.
T5 466-601 Sentence denotes A consanguineous family is described in which 2 siblings, born after pregnancies complicated by oligohydramnios were affected with RTD.
T6 602-651 Sentence denotes Patients were small for gestational age at birth.
T7 652-780 Sentence denotes The first patient died after a few hours, the second after a few days of life, with persistent anuria unresponsive to treatment.
T8 781-916 Sentence denotes Histologically, there was marked reduction in the number of proximal tubule sections and no renin was detected by immunohistochemistry.
T9 917-999 Sentence denotes An homozygous mutation of the gene encoding renin was identified in both patients.
T10 1000-1246 Sentence denotes This study underlines the interest of the histological examination of the kidney for the diagnostic of RTD in anuric fetuses and newborns, and the possibility of mutation analysis of RAS genes for genetic counselling and early prenatal diagnosis.

performance-test

Id Subject Object Predicate Lexical cue
PD-UBERON-AE-B_T1 448-464 http://purl.obolibrary.org/obo/UBERON_0004134 denotes proximal tubules
PD-UBERON-AE-B_T2 841-856 http://purl.obolibrary.org/obo/UBERON_0004134 denotes proximal tubule
PD-UBERON-AE-B_T3 1074-1080 http://purl.obolibrary.org/obo/UBERON_0002113 denotes kidney

QFMC_MEDLINE

Id Subject Object Predicate Lexical cue
T1 90-139 DISO denotes Dysgénésie tubulaire rénale autosomique récessive
T1c 90-139 UMLS:C0266313 denotes Dysgénésie tubulaire rénale autosomique récessive
T2 111-117 ANAT denotes rénale
T2c 111-117 UMLS:C0022646 denotes rénale
T3 141-146 PROC denotes étude
T3c 141-146 UMLS:C2603343 denotes étude
#1 T1 T1c Normalization Dysgénésie tubulaire rénale autosomique récessive,Dysgénésie tubulaire rénale autosomique récessive
#2 T2 T2c Normalization rénale,rénale
#3 T3 T3c Normalization étude,étude