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PubMed:1376553 JSONTXT 16 Projects

Annnotations TAB TSV DIC JSON TextAE Lectin_function IAV-Glycan

Id Subject Object Predicate Lexical cue
TextSentencer_T1 0-106 Sentence denotes New variant in exon 3 of the proteolipid protein (PLP) gene in a family with Pelizaeus-Merzbacher disease.
T1 0-106 Sentence denotes New variant in exon 3 of the proteolipid protein (PLP) gene in a family with Pelizaeus-Merzbacher disease.
TextSentencer_T2 107-276 Sentence denotes A C--greater than G transversion has been found in exon 3 of the PLP gene of affected males and their mother in a single sibship with Pelizaeus-merzbacher disease (PMD).
T2 107-276 Sentence denotes A C--greater than G transversion has been found in exon 3 of the PLP gene of affected males and their mother in a single sibship with Pelizaeus-merzbacher disease (PMD).
TextSentencer_T3 277-433 Sentence denotes The transversion should not result in an amino acid change in the protein but it does result in the loss of a HaeIII restriction endonuclease cleavage site.
T3 277-433 Sentence denotes The transversion should not result in an amino acid change in the protein but it does result in the loss of a HaeIII restriction endonuclease cleavage site.
TextSentencer_T4 434-483 Sentence denotes It is concordant with the disease in this family.
T4 434-483 Sentence denotes It is concordant with the disease in this family.
TextSentencer_T5 484-555 Sentence denotes One-hundred-ten unrelated X chromosomes are negative for this mutation.
T5 484-555 Sentence denotes One-hundred-ten unrelated X chromosomes are negative for this mutation.
TextSentencer_T6 556-630 Sentence denotes No other sequence defect was found in the PLP exons of the affected males.
T6 556-630 Sentence denotes No other sequence defect was found in the PLP exons of the affected males.
TextSentencer_T7 631-753 Sentence denotes The cause of disease in this family remains unknown, but the association between this rare mutation and PMD is intriguing.
T7 631-753 Sentence denotes The cause of disease in this family remains unknown, but the association between this rare mutation and PMD is intriguing.
TextSentencer_T8 754-831 Sentence denotes The mutation can serve as a marker for following segregation of the PLP gene.
T8 754-831 Sentence denotes The mutation can serve as a marker for following segregation of the PLP gene.