| Id |
Subject |
Object |
Predicate |
Lexical cue |
| 17502119-0#0#3#gene472 |
600-614 |
gene472 |
denotes |
ATERIALS AND M |
| 17502119-0#43#58#diseaseC0376358 |
1687-1884 |
diseaseC0376358 |
denotes |
p=0.61), IIEF-15 score (p=0.78), IIEF-5 score (p=0.83), and EF score (p=0.80), respectively.
CONCLUSIONS: The ATM missense variant P1054R confers an about twofold increased risk for prostate cancer |
| 17502119-0#43#58#diseaseC0600139 |
1687-1884 |
diseaseC0600139 |
denotes |
p=0.61), IIEF-15 score (p=0.78), IIEF-5 score (p=0.83), and EF score (p=0.80), respectively.
CONCLUSIONS: The ATM missense variant P1054R confers an about twofold increased risk for prostate cancer |
| 0#3#gene47243#58#diseaseC0376358 |
17502119-0#0#3#gene472 |
17502119-0#43#58#diseaseC0376358 |
associated_with |
ATERIALS AND M,"p=0.61), IIEF-15 score (p=0.78), IIEF-5 score (p=0.83), and EF score (p=0.80), respectively.
CONCLUSIONS: The ATM missense variant P1054R confers an about twofold increased risk for prostate cancer" |
| 0#3#gene47243#58#diseaseC0600139 |
17502119-0#0#3#gene472 |
17502119-0#43#58#diseaseC0600139 |
associated_with |
ATERIALS AND M,"p=0.61), IIEF-15 score (p=0.78), IIEF-5 score (p=0.83), and EF score (p=0.80), respectively.
CONCLUSIONS: The ATM missense variant P1054R confers an about twofold increased risk for prostate cancer" |
