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PubMed:18773291 JSONTXT 24 Projects

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Id Subject Object Predicate Lexical cue
TextSentencer_T1 0-50 Sentence denotes Dystroglycan glycosylation and muscular dystrophy.
T1 0-50 Sentence denotes Dystroglycan glycosylation and muscular dystrophy.
TextSentencer_T2 51-205 Sentence denotes Dystroglycan is an integral member of the skeletal muscle dystrophin glycoprotein complex, which links dystrophin to proteins in the extracellular matrix.
T2 51-205 Sentence denotes Dystroglycan is an integral member of the skeletal muscle dystrophin glycoprotein complex, which links dystrophin to proteins in the extracellular matrix.
TextSentencer_T3 206-358 Sentence denotes Recently, a group of human muscular dystrophy disorders have been demonstrated to result from defective glycosylation of the alpha-dystroglycan subunit.
T3 206-358 Sentence denotes Recently, a group of human muscular dystrophy disorders have been demonstrated to result from defective glycosylation of the alpha-dystroglycan subunit.
TextSentencer_T4 359-520 Sentence denotes Genetic studies of these diseases have identified six genes that encode proteins required for the synthesis of essential carbohydrate structures on dystroglycan.
T4 359-520 Sentence denotes Genetic studies of these diseases have identified six genes that encode proteins required for the synthesis of essential carbohydrate structures on dystroglycan.
TextSentencer_T5 521-575 Sentence denotes Here we highlight their known or postulated functions.
T5 521-575 Sentence denotes Here we highlight their known or postulated functions.
TextSentencer_T6 576-734 Sentence denotes This glycosylation pathway appears to be highly specific (dystroglycan is the only substrate identified thus far) and to be highly conserved during evolution.
T6 576-734 Sentence denotes This glycosylation pathway appears to be highly specific (dystroglycan is the only substrate identified thus far) and to be highly conserved during evolution.