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PubMed:10484772 JSONTXT 17 Projects

Annnotations TAB TSV DIC JSON TextAE Lectin_function IAV-Glycan

Id Subject Object Predicate Lexical cue
TextSentencer_T1 0-151 Sentence denotes Coats' disease of the retina (unilateral retinal telangiectasis) caused by somatic mutation in the NDP gene: a role for norrin in retinal angiogenesis.
T1 0-151 Sentence denotes Coats' disease of the retina (unilateral retinal telangiectasis) caused by somatic mutation in the NDP gene: a role for norrin in retinal angiogenesis.
TextSentencer_T2 152-365 Sentence denotes Coats' disease is characterized by abnormal retinal vascular development (so-called 'retinal telangiectasis') which results in massive intraretinal and subretinal lipid accumulation (exudative retinal detachment).
T2 152-365 Sentence denotes Coats' disease is characterized by abnormal retinal vascular development (so-called 'retinal telangiectasis') which results in massive intraretinal and subretinal lipid accumulation (exudative retinal detachment).
TextSentencer_T3 366-463 Sentence denotes The classical form of Coats' disease is almost invariably isolated, unilateral and seen in males.
T3 366-463 Sentence denotes The classical form of Coats' disease is almost invariably isolated, unilateral and seen in males.
TextSentencer_T4 464-564 Sentence denotes A female with a unilateral variant of Coats' disease gave birth to a son affected by Norrie disease.
T4 464-564 Sentence denotes A female with a unilateral variant of Coats' disease gave birth to a son affected by Norrie disease.
TextSentencer_T5 565-639 Sentence denotes Both carried a missense mutation within the NDP gene on chromosome Xp11.2.
T5 565-639 Sentence denotes Both carried a missense mutation within the NDP gene on chromosome Xp11.2.
TextSentencer_T6 640-835 Sentence denotes Subsequently analysis of the retinas of nine enucleated eyes from males with Coats' disease demonstrated in one a somatic mutation in the NDP gene which was not present within non-retinal tissue.
T6 640-835 Sentence denotes Subsequently analysis of the retinas of nine enucleated eyes from males with Coats' disease demonstrated in one a somatic mutation in the NDP gene which was not present within non-retinal tissue.
TextSentencer_T7 836-1030 Sentence denotes We suggest that Coats' telangiectasis is secondary to somatic mutation in the NDP gene which results in a deficiency of norrin (the protein product of the NDP gene) within the developing retina.
T7 836-1030 Sentence denotes We suggest that Coats' telangiectasis is secondary to somatic mutation in the NDP gene which results in a deficiency of norrin (the protein product of the NDP gene) within the developing retina.
TextSentencer_T8 1031-1128 Sentence denotes This supports recent observations that the protein is critical for normal retinal vasculogenesis.
T8 1031-1128 Sentence denotes This supports recent observations that the protein is critical for normal retinal vasculogenesis.