PubMed:8266996
Annnotations
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 |