| Id |
Subject |
Object |
Predicate |
Lexical cue |
| 10087990-0#0#20#gene7037 |
266-431 |
gene7037 |
denotes |
This suggests a possibility that these patients may have a mutation in other genes in the same pathway as HFE. We analyzed the cDNA sequences of transferrin receptor |
| 10087990-0#42#68#diseaseC0392514 |
815-988 |
diseaseC0392514 |
denotes |
his amino acid substitution was a rather common polymorphism in the general population (49%) and its frequency did not significantly differ in the hereditary hemochromatosis |
| 10087990-5#148#174#diseaseC0392514 |
962-988 |
diseaseC0392514 |
denotes |
hereditary hemochromatosis |
| 10087990-5#176#178#diseaseC0392514 |
990-992 |
diseaseC0392514 |
denotes |
HH |
| 10087990-5#207#210#gene3077 |
1021-1024 |
gene3077 |
denotes |
HFE |
| 0#20#gene703742#68#diseaseC0392514 |
10087990-0#0#20#gene7037 |
10087990-0#42#68#diseaseC0392514 |
associated_with |
This suggests a possibility that these patients may have a mutation in other genes in the same pathway as HFE. We analyzed the cDNA sequences of transferrin receptor,his amino acid substitution was a rather common polymorphism in the general population (49%) and its frequency did not significantly differ in the hereditary hemochromatosis |
| 207#210#gene3077148#174#diseaseC0392514 |
10087990-5#207#210#gene3077 |
10087990-5#148#174#diseaseC0392514 |
associated_with |
HFE,hereditary hemochromatosis |
| 207#210#gene3077176#178#diseaseC0392514 |
10087990-5#207#210#gene3077 |
10087990-5#176#178#diseaseC0392514 |
associated_with |
HFE,HH |
