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PubMed:7993996 JSONTXT 10 Projects

Annnotations TAB TSV DIC JSON TextAE Lectin_function IAV-Glycan

Id Subject Object Predicate Lexical cue
TextSentencer_T1 0-98 Sentence denotes Mutations in the vasopressin V2 receptor gene in two families with nephrogenic diabetes insipidus.
T1 0-98 Sentence denotes Mutations in the vasopressin V2 receptor gene in two families with nephrogenic diabetes insipidus.
TextSentencer_T2 99-308 Sentence denotes Congenital nephrogenic diabetes insipidus (CNDI) is a rare X-linked disorder in which the renal collecting duct is unresponsive to arginine vasopressin, and thus, the urine is consistently hypotonic to plasma.
T2 99-308 Sentence denotes Congenital nephrogenic diabetes insipidus (CNDI) is a rare X-linked disorder in which the renal collecting duct is unresponsive to arginine vasopressin, and thus, the urine is consistently hypotonic to plasma.
TextSentencer_T3 309-440 Sentence denotes As a result, affected individuals are unable to concentrate urine and suffer from episodes of severe dehydration and hypernatremia.
T3 309-440 Sentence denotes As a result, affected individuals are unable to concentrate urine and suffer from episodes of severe dehydration and hypernatremia.
TextSentencer_T4 441-554 Sentence denotes Recently, the association between arginine vasopressin V2 receptor gene mutations and CNDI has been demonstrated.
T4 441-554 Sentence denotes Recently, the association between arginine vasopressin V2 receptor gene mutations and CNDI has been demonstrated.
TextSentencer_T5 555-686 Sentence denotes In this report, two additional novel molecular defects of the arginine vasopressin V2 receptor gene in CNDI families are described.
T5 555-686 Sentence denotes In this report, two additional novel molecular defects of the arginine vasopressin V2 receptor gene in CNDI families are described.
TextSentencer_T6 687-801 Sentence denotes In one family, the affected individual demonstrated a G-->T transversion causing a nonsense mutation in codon 231.
T6 687-801 Sentence denotes In one family, the affected individual demonstrated a G-->T transversion causing a nonsense mutation in codon 231.
TextSentencer_T7 802-950 Sentence denotes This mutation results in a glutamic acid becoming a termination codon, causing premature termination and truncation of the encoded receptor protein.
T7 802-950 Sentence denotes This mutation results in a glutamic acid becoming a termination codon, causing premature termination and truncation of the encoded receptor protein.
TextSentencer_T8 951-1047 Sentence denotes This mutation causes a NciI site within the gene to be abolished and a BsaWI site to be created.
T8 951-1047 Sentence denotes This mutation causes a NciI site within the gene to be abolished and a BsaWI site to be created.
TextSentencer_T9 1048-1206 Sentence denotes In the second family, affected individuals showed a 28-basepair duplicating insertion in the very beginning of exon 2 down-stream of the splice acceptor site.
T9 1048-1206 Sentence denotes In the second family, affected individuals showed a 28-basepair duplicating insertion in the very beginning of exon 2 down-stream of the splice acceptor site.
TextSentencer_T10 1207-1389 Sentence denotes It was hypothesized that an insertion mutagenesis mechanism involves the formation of a stem-loop structure within the newly synthesized DNA strand, followed by a slipped mispairing.
T10 1207-1389 Sentence denotes It was hypothesized that an insertion mutagenesis mechanism involves the formation of a stem-loop structure within the newly synthesized DNA strand, followed by a slipped mispairing.
TextSentencer_T11 1390-1492 Sentence denotes This may be a general mechanism for the deletion or insertion of repeated sequences within the genome.
T11 1390-1492 Sentence denotes This may be a general mechanism for the deletion or insertion of repeated sequences within the genome.
TextSentencer_T12 1493-1667 Sentence denotes Recent data show that G-protein-coupled receptors are susceptible to many different mutations that often result in the loss of function, causing a similar clinical phenotype.
T12 1493-1667 Sentence denotes Recent data show that G-protein-coupled receptors are susceptible to many different mutations that often result in the loss of function, causing a similar clinical phenotype.