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PubMed:7643352 JSONTXT 11 Projects

Annnotations TAB TSV DIC JSON TextAE Lectin_function IAV-Glycan

Id Subject Object Predicate Lexical cue
TextSentencer_T1 0-120 Sentence denotes A new X linked recessive deafness syndrome with blindness, dystonia, fractures, and mental deficiency is linked to Xq22.
T1 0-120 Sentence denotes A new X linked recessive deafness syndrome with blindness, dystonia, fractures, and mental deficiency is linked to Xq22.
TextSentencer_T2 121-198 Sentence denotes X linked recessive deafness accounts for only 1.7% of all childhood deafness.
T2 121-198 Sentence denotes X linked recessive deafness accounts for only 1.7% of all childhood deafness.
TextSentencer_T3 199-340 Sentence denotes Only a few of the at least 28 different X linked syndromes associated with hearing impairment have been characterised at the molecular level.
T3 199-340 Sentence denotes Only a few of the at least 28 different X linked syndromes associated with hearing impairment have been characterised at the molecular level.
TextSentencer_T4 341-497 Sentence denotes In 1960, a large Norwegian family was reported with early onset progressive sensorineural deafness, which was indexed in McKusick as DFN-1, McKusick 304700.
T4 341-497 Sentence denotes In 1960, a large Norwegian family was reported with early onset progressive sensorineural deafness, which was indexed in McKusick as DFN-1, McKusick 304700.
TextSentencer_T5 498-549 Sentence denotes No associated symptoms were described at that time.
T5 498-549 Sentence denotes No associated symptoms were described at that time.
TextSentencer_T6 550-592 Sentence denotes This family has been restudied clinically.
T6 550-592 Sentence denotes This family has been restudied clinically.
TextSentencer_T7 593-772 Sentence denotes Extensive neurological, neurophysiological, neuroradiological, and biochemical, as well as molecular techniques, have been applied to characterise the X linked recessive syndrome.
T7 593-772 Sentence denotes Extensive neurological, neurophysiological, neuroradiological, and biochemical, as well as molecular techniques, have been applied to characterise the X linked recessive syndrome.
TextSentencer_T8 773-978 Sentence denotes The family history and extensive characterisation of 16 affected males in five generations confirmed the X linked recessive inheritance and the postlingual progressive nature of the sensorineural deafness.
T8 773-978 Sentence denotes The family history and extensive characterisation of 16 affected males in five generations confirmed the X linked recessive inheritance and the postlingual progressive nature of the sensorineural deafness.
TextSentencer_T9 979-1070 Sentence denotes Some obligate carrier females showed signs of minor neuropathy and mild hearing impairment.
T9 979-1070 Sentence denotes Some obligate carrier females showed signs of minor neuropathy and mild hearing impairment.
TextSentencer_T10 1071-1294 Sentence denotes Restudy of the original DFN-1 family showed that the deafness is part of a progressive X linked recessive syndrome, which includes visual disability leading to cortical blindness, dystonia, fractures, and mental deficiency.
T10 1071-1294 Sentence denotes Restudy of the original DFN-1 family showed that the deafness is part of a progressive X linked recessive syndrome, which includes visual disability leading to cortical blindness, dystonia, fractures, and mental deficiency.
TextSentencer_T11 1295-1417 Sentence denotes Linkage analysis indicated that the gene was linked to locus DXS101 in Xq22 with a lod score of 5.37 (zero recombination).
T11 1295-1417 Sentence denotes Linkage analysis indicated that the gene was linked to locus DXS101 in Xq22 with a lod score of 5.37 (zero recombination).
TextSentencer_T12 1418-1567 Sentence denotes Based on lod-1 support interval of the multipoint analysis, the gene is located in a region spanning from 5 cM proximal to 3 cM distal to this locus.
T12 1418-1567 Sentence denotes Based on lod-1 support interval of the multipoint analysis, the gene is located in a region spanning from 5 cM proximal to 3 cM distal to this locus.
TextSentencer_T13 1568-1839 Sentence denotes As the proteolipid protein gene (PLP) is within this region and mutations have been shown to be associated with non-classical PMD (Pelizaeus-Merzbacher disease), such as complex X linked hereditary spastic paraplegia, PLP may represent a candidate gene for this disorder.
T13 1568-1839 Sentence denotes As the proteolipid protein gene (PLP) is within this region and mutations have been shown to be associated with non-classical PMD (Pelizaeus-Merzbacher disease), such as complex X linked hereditary spastic paraplegia, PLP may represent a candidate gene for this disorder.
TextSentencer_T14 1840-2062 Sentence denotes This family represents a new syndrome (Mohr-Tranebjaerg syndrome, MTS) and provides significant new information about a new X linked recessive sydromic type of deafness which was previously thought to be isolated deafness.
T14 1840-2062 Sentence denotes This family represents a new syndrome (Mohr-Tranebjaerg syndrome, MTS) and provides significant new information about a new X linked recessive sydromic type of deafness which was previously thought to be isolated deafness.