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sentences

Id Subject Object Predicate Lexical cue
TextSentencer_T1 0-119 Sentence denotes Common sequence motifs at the rearrangement sites of a constitutional X/autosome translocation and associated deletion.
TextSentencer_T2 120-239 Sentence denotes Reciprocal chromosome translocations are common de novo rearrangements that occur randomly throughout the human genome.
TextSentencer_T3 240-470 Sentence denotes To learn about causative mechanisms, we have cloned and sequenced the breakpoints of a cytologically balanced constitutional reciprocal translocation, t(X;4)(p21.2;q31.22), present in a girl with Duchenne muscular dystrophy (DMD).
TextSentencer_T4 471-655 Sentence denotes Physical mapping of the derivative chromosomes, after their separation in somatic cell hybrids, reveals that the translocation disrupts the DMD gene in Xp21 within the 18-kb intron 16.
TextSentencer_T5 656-913 Sentence denotes Restriction mapping and sequencing of clones that span both translocation breakpoints as well as the corresponding normal regions indicate the loss of approximately 5 kb in the formation of the derivative X chromosome, with 4-6 bp deleted from chromosome 4.
TextSentencer_T6 914-1090 Sentence denotes RFLP and Southern analyses indicate that the de novo translocation is a paternal origin and that the father's X chromosome contains the DNA that is deleted in the derivative X.
TextSentencer_T7 1091-1229 Sentence denotes Most likely, deletion and translation arose simultaneously from a complex rearrangement event that involves three chromosomal breakpoints.
TextSentencer_T8 1230-1297 Sentence denotes Short regions of sequence homology were present at the three sites.
TextSentencer_T9 1298-1454 Sentence denotes A 5-bp sequence, GGAAT, found exactly at the translocation breakpoints on both normal chromosomes X and 4, has been preserved only on the der(4) chromosome.
TextSentencer_T10 1455-1688 Sentence denotes It is likely that the X-derived sequence GGAATCA has been lost in the formation of the der(X) chromosome, as it matches an inverted GAATCA sequence present on the opposite strand exactly at the other end of the deleted 5-kb fragment.
TextSentencer_T11 1689-1883 Sentence denotes These findings suggest a possible mechanism which may have juxtaposed the three sites and mediated sequence-specific breakage and recombination between nonhomologous chromosomes in male meiosis.
T1 0-119 Sentence denotes Common sequence motifs at the rearrangement sites of a constitutional X/autosome translocation and associated deletion.
T2 120-239 Sentence denotes Reciprocal chromosome translocations are common de novo rearrangements that occur randomly throughout the human genome.
T3 240-470 Sentence denotes To learn about causative mechanisms, we have cloned and sequenced the breakpoints of a cytologically balanced constitutional reciprocal translocation, t(X;4)(p21.2;q31.22), present in a girl with Duchenne muscular dystrophy (DMD).
T4 471-655 Sentence denotes Physical mapping of the derivative chromosomes, after their separation in somatic cell hybrids, reveals that the translocation disrupts the DMD gene in Xp21 within the 18-kb intron 16.
T5 656-913 Sentence denotes Restriction mapping and sequencing of clones that span both translocation breakpoints as well as the corresponding normal regions indicate the loss of approximately 5 kb in the formation of the derivative X chromosome, with 4-6 bp deleted from chromosome 4.
T6 914-1090 Sentence denotes RFLP and Southern analyses indicate that the de novo translocation is a paternal origin and that the father's X chromosome contains the DNA that is deleted in the derivative X.
T7 1091-1229 Sentence denotes Most likely, deletion and translation arose simultaneously from a complex rearrangement event that involves three chromosomal breakpoints.
T8 1230-1297 Sentence denotes Short regions of sequence homology were present at the three sites.
T9 1298-1454 Sentence denotes A 5-bp sequence, GGAAT, found exactly at the translocation breakpoints on both normal chromosomes X and 4, has been preserved only on the der(4) chromosome.
T10 1455-1688 Sentence denotes It is likely that the X-derived sequence GGAATCA has been lost in the formation of the der(X) chromosome, as it matches an inverted GAATCA sequence present on the opposite strand exactly at the other end of the deleted 5-kb fragment.
T11 1689-1883 Sentence denotes These findings suggest a possible mechanism which may have juxtaposed the three sites and mediated sequence-specific breakage and recombination between nonhomologous chromosomes in male meiosis.

PubCasesHPO

Id Subject Object Predicate Lexical cue
AB1 445-463 HP:0003560 denotes muscular dystrophy

PubCasesORDO

Id Subject Object Predicate Lexical cue
AB1 436-463 ORDO:98896 denotes Duchenne muscular dystrophy
AB2 465-468 ORDO:98896 denotes DMD
AB3 611-614 ORDO:98896 denotes DMD

NCBIDiseaseCorpus

Id Subject Object Predicate Lexical cue
T1 436-463 SpecificDisease:D020388 denotes Duchenne muscular dystrophy
T2 465-468 SpecificDisease:D020388 denotes DMD
T3 611-614 Modifier:D020388 denotes DMD

NCBI-Disease-Train

Id Subject Object Predicate Lexical cue database_id
T2041 436-463 SpecificDisease denotes Duchenne muscular dystrophy D020388
T2042 465-468 SpecificDisease denotes DMD D020388
T2043 611-614 Modifier denotes DMD D020388

NCBI-Disease-Corpus-All

Id Subject Object Predicate Lexical cue database_id
T2041 436-463 SpecificDisease denotes Duchenne muscular dystrophy D020388
T2042 465-468 SpecificDisease denotes DMD D020388
T2043 611-614 Modifier denotes DMD D020388

NCBI-Disease-Corpus-2stage-All

Id Subject Object Predicate Lexical cue
T1 436-463 SpecificDisease denotes Duchenne muscular dystrophy
T2 465-468 SpecificDisease denotes DMD
T3 611-614 Modifier denotes DMD

NCBI-Disease-Corpus-rezarta-All

Id Subject Object Predicate Lexical cue
T1 436-463 SpecificDisease denotes Duchenne muscular dystrophy
T2 465-468 SpecificDisease denotes DMD
T3 611-614 Modifier denotes DMD

NCBI-Disease-Corpus-4oGuideline-All

Id Subject Object Predicate Lexical cue
T1 436-463 SpecificDisease denotes Duchenne muscular dystrophy
T2 465-468 SpecificDisease denotes DMD
T3 611-614 Modifier denotes DMD

NCBI-Disease-Corpus-Simple-All

Id Subject Object Predicate Lexical cue
T1 436-463 SpecificDisease denotes Duchenne muscular dystrophy
T2 465-468 SpecificDisease denotes DMD
T3 611-619 SpecificDisease denotes DMD gene