| Id |
Subject |
Object |
Predicate |
Lexical cue |
| TextSentencer_T1 |
0-73 |
Sentence |
denotes |
A high incidence of BRCA1 mutations in 20 breast-ovarian cancer families. |
| T1 |
0-73 |
Sentence |
denotes |
A high incidence of BRCA1 mutations in 20 breast-ovarian cancer families. |
| TextSentencer_T2 |
74-244 |
Sentence |
denotes |
We have analyzed 20 breast-ovarian cancer families, the majority of which show positive evidence of linkage to chromosome 17q12 for germ-line mutations in the BRCA1 gene. |
| T2 |
74-244 |
Sentence |
denotes |
We have analyzed 20 breast-ovarian cancer families, the majority of which show positive evidence of linkage to chromosome 17q12 for germ-line mutations in the BRCA1 gene. |
| TextSentencer_T3 |
245-406 |
Sentence |
denotes |
BRCA1 mutations cosegregating with breast and ovarian cancer susceptibility were identified in 16 families, including 1 family with a case of male breast cancer. |
| T3 |
245-406 |
Sentence |
denotes |
BRCA1 mutations cosegregating with breast and ovarian cancer susceptibility were identified in 16 families, including 1 family with a case of male breast cancer. |
| TextSentencer_T4 |
407-465 |
Sentence |
denotes |
Nine of these mutations have not been reported previously. |
| T4 |
407-465 |
Sentence |
denotes |
Nine of these mutations have not been reported previously. |
| TextSentencer_T5 |
466-632 |
Sentence |
denotes |
The majority of mutations were found to generate a premature stop codon leading to the formation of a truncated BRCA1 protein of 2%-88% of the expected normal length. |
| T5 |
466-632 |
Sentence |
denotes |
The majority of mutations were found to generate a premature stop codon leading to the formation of a truncated BRCA1 protein of 2%-88% of the expected normal length. |
| TextSentencer_T6 |
633-678 |
Sentence |
denotes |
Two mutations altered the RING finger domain. |
| T6 |
633-678 |
Sentence |
denotes |
Two mutations altered the RING finger domain. |
| TextSentencer_T7 |
679-891 |
Sentence |
denotes |
Sequencing of genomic DNA led to the identification of a mutation in the coding region of BRCA1 in 12 families, and cDNA analysis revealed an abnormal or missing BRCA1 transcript in 4 of the 8 remaining families. |
| T7 |
679-891 |
Sentence |
denotes |
Sequencing of genomic DNA led to the identification of a mutation in the coding region of BRCA1 in 12 families, and cDNA analysis revealed an abnormal or missing BRCA1 transcript in 4 of the 8 remaining families. |
| TextSentencer_T8 |
892-979 |
Sentence |
denotes |
A total of eight mutations were associated with a reduced quantity of BRCA1 transcript. |
| T8 |
892-979 |
Sentence |
denotes |
A total of eight mutations were associated with a reduced quantity of BRCA1 transcript. |
| TextSentencer_T9 |
980-1094 |
Sentence |
denotes |
We were unable to detect BRCA1 mutations in 4 of the 20 families, but only 1 of these was clearly linked to BRCA1. |
| T9 |
980-1094 |
Sentence |
denotes |
We were unable to detect BRCA1 mutations in 4 of the 20 families, but only 1 of these was clearly linked to BRCA1. |
| TextSentencer_T10 |
1095-1251 |
Sentence |
denotes |
It is expected that the majority of clear examples of the breast-ovarian syndrome will be associated with germ-line mutations in the coding region of BRCA1. |
| T10 |
1095-1251 |
Sentence |
denotes |
It is expected that the majority of clear examples of the breast-ovarian syndrome will be associated with germ-line mutations in the coding region of BRCA1. |