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PubMed:8266996 JSONTXT

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sentences

Id Subject Object Predicate Lexical cue
TextSentencer_T1 0-148 Sentence denotes Difference in methylation patterns within the D15S9 region of chromosome 15q11-13 in first cousins with Angelman syndrome and Prader-Willi syndrome.
TextSentencer_T2 149-268 Sentence denotes Abnormalities of chromosome region 15q11-13 are associated with Angelman syndrome (AS) and Prader-Willi syndrome (PWS).
TextSentencer_T3 269-477 Sentence denotes Differences between the methylation patterns of the region of chromosome 15q11-13 which hybridizes to the highly conserved DNA, DN34, in normal individuals and in patients with AS and PWS have been described.
TextSentencer_T4 478-611 Sentence denotes We report on a family in which first cousins are affected by AS and PWS as a result of a familial paracentric inversion of 15q11-q13.
TextSentencer_T5 612-859 Sentence denotes The results of the studies on this family demonstrate the differences in the methylation patterns in the 2 conditions and the phenomenon of genomic imprinting, whereby genetic information is expressed differently dependent on the parent of origin.
T1 0-148 Sentence denotes Difference in methylation patterns within the D15S9 region of chromosome 15q11-13 in first cousins with Angelman syndrome and Prader-Willi syndrome.
T2 149-268 Sentence denotes Abnormalities of chromosome region 15q11-13 are associated with Angelman syndrome (AS) and Prader-Willi syndrome (PWS).
T3 269-477 Sentence denotes Differences between the methylation patterns of the region of chromosome 15q11-13 which hybridizes to the highly conserved DNA, DN34, in normal individuals and in patients with AS and PWS have been described.
T4 478-611 Sentence denotes We report on a family in which first cousins are affected by AS and PWS as a result of a familial paracentric inversion of 15q11-q13.
T5 612-859 Sentence denotes The results of the studies on this family demonstrate the differences in the methylation patterns in the 2 conditions and the phenomenon of genomic imprinting, whereby genetic information is expressed differently dependent on the parent of origin.

DisGeNET

Id Subject Object Predicate Lexical cue
T0 46-51 gene:7681 denotes D15S9
T1 104-121 disease:C0162635 denotes Angelman syndrome
T2 46-51 gene:7681 denotes D15S9
T3 126-147 disease:C0032897 denotes Prader-Willi syndrome
R1 T0 T1 associated_with D15S9,Angelman syndrome
R2 T2 T3 associated_with D15S9,Prader-Willi syndrome

PubCasesORDO

Id Subject Object Predicate Lexical cue
AB1 213-230 ORDO:72 denotes Angelman syndrome
AB2 240-261 ORDO:739 denotes Prader-Willi syndrome
TI1 104-121 ORDO:72 denotes Angelman syndrome
TI2 126-147 ORDO:739 denotes Prader-Willi syndrome

NCBIDiseaseCorpus

Id Subject Object Predicate Lexical cue
T1 104-121 SpecificDisease:D017204 denotes Angelman syndrome
T2 126-147 SpecificDisease:D011218 denotes Prader-Willi syndrome
T3 213-230 SpecificDisease:D017204 denotes Angelman syndrome
T4 232-234 SpecificDisease:D017204 denotes AS
T5 240-261 SpecificDisease:D011218 denotes Prader-Willi syndrome
T6 263-266 SpecificDisease:D011218 denotes PWS
T7 446-448 SpecificDisease:D017204 denotes AS
T8 453-456 SpecificDisease:D011218 denotes PWS
T9 539-541 SpecificDisease:D017204 denotes AS
T10 546-549 SpecificDisease:D011218 denotes PWS

NCBI-Disease-Train

Id Subject Object Predicate Lexical cue database_id
T4631 104-121 SpecificDisease denotes Angelman syndrome D017204
T4632 126-147 SpecificDisease denotes Prader-Willi syndrome D011218
T4633 213-230 SpecificDisease denotes Angelman syndrome D017204
T4634 232-234 SpecificDisease denotes AS D017204
T4635 240-261 SpecificDisease denotes Prader-Willi syndrome D011218
T4636 263-266 SpecificDisease denotes PWS D011218
T4637 446-448 SpecificDisease denotes AS D017204
T4638 453-456 SpecificDisease denotes PWS D011218
T4639 539-541 SpecificDisease denotes AS D017204
T4640 546-549 SpecificDisease denotes PWS D011218

NCBI-Disease-Corpus-All

Id Subject Object Predicate Lexical cue database_id
T4631 104-121 SpecificDisease denotes Angelman syndrome D017204
T4632 126-147 SpecificDisease denotes Prader-Willi syndrome D011218
T4633 213-230 SpecificDisease denotes Angelman syndrome D017204
T4634 232-234 SpecificDisease denotes AS D017204
T4635 240-261 SpecificDisease denotes Prader-Willi syndrome D011218
T4636 263-266 SpecificDisease denotes PWS D011218
T4637 446-448 SpecificDisease denotes AS D017204
T4638 453-456 SpecificDisease denotes PWS D011218
T4639 539-541 SpecificDisease denotes AS D017204
T4640 546-549 SpecificDisease denotes PWS D011218

NCBI-Disease-Corpus-2stage-All

Id Subject Object Predicate Lexical cue
T1 104-121 SpecificDisease denotes Angelman syndrome
T2 126-147 SpecificDisease denotes Prader-Willi syndrome
T3 213-230 SpecificDisease denotes Angelman syndrome
T4 232-234 SpecificDisease denotes AS
T5 240-261 SpecificDisease denotes Prader-Willi syndrome
T6 263-266 SpecificDisease denotes PWS
T7 446-448 SpecificDisease denotes AS
T8 453-456 SpecificDisease denotes PWS
T9 539-541 SpecificDisease denotes AS
T10 546-549 SpecificDisease denotes PWS

NCBI-Disease-Corpus-rezarta-All

Id Subject Object Predicate Lexical cue
T1 104-121 SpecificDisease denotes Angelman syndrome
T2 126-147 SpecificDisease denotes Prader-Willi syndrome
T3 213-230 SpecificDisease denotes Angelman syndrome
T4 232-234 SpecificDisease denotes AS
T5 240-261 SpecificDisease denotes Prader-Willi syndrome
T6 263-266 SpecificDisease denotes PWS
T7 446-448 SpecificDisease denotes AS
T8 453-456 SpecificDisease denotes PWS
T9 539-541 SpecificDisease denotes AS
T10 546-549 SpecificDisease denotes PWS

NCBI-Disease-Corpus-4oGuideline-All

Id Subject Object Predicate Lexical cue
T1 104-121 SpecificDisease denotes Angelman syndrome
T2 126-147 SpecificDisease denotes Prader-Willi syndrome
T3 213-235 SpecificDisease denotes Angelman syndrome (AS)
T4 240-267 SpecificDisease denotes Prader-Willi syndrome (PWS)
T5 446-448 SpecificDisease denotes AS
T6 453-456 SpecificDisease denotes PWS
T7 539-541 SpecificDisease denotes AS
T8 546-549 SpecificDisease denotes PWS

NCBI-Disease-Corpus-Simple-All

Id Subject Object Predicate Lexical cue
T1 104-121 SpecificDisease denotes Angelman syndrome
T2 126-147 SpecificDisease denotes Prader-Willi syndrome
T3 213-235 SpecificDisease denotes Angelman syndrome (AS)
T4 240-267 SpecificDisease denotes Prader-Willi syndrome (PWS)
T5 446-448 SpecificDisease denotes AS
T6 453-456 SpecificDisease denotes PWS
T7 539-541 SpecificDisease denotes AS
T8 546-549 SpecificDisease denotes PWS