PubMed:26846579
Annnotations
Inflammaging
| Id | Subject | Object | Predicate | Lexical cue |
|---|---|---|---|---|
| T1 | 0-58 | Sentence | denotes | The role of inflammation in the pathology of preeclampsia. |
| T2 | 59-190 | Sentence | denotes | Preeclampsia (PE) affects 5-7% of all pregnancies in the United States and is the leading cause of maternal and prenatal morbidity. |
| T3 | 191-316 | Sentence | denotes | PE is associated with hypertension after week 20 of gestation, decreased renal function and small-for-gestational-age babies. |
| T4 | 317-393 | Sentence | denotes | Women with PE exhibit chronic inflammation and production of autoantibodies. |
| T5 | 394-642 | Sentence | denotes | It is hypothesized that during PE, placental ischaemia occurs as a result of shallow trophoblast invasion which is associated with an immune imbalance where pro-inflammatory CD4(+) T-cells are increased and T regulatory cells (Tregs) are decreased. |
| T6 | 643-769 | Sentence | denotes | This imbalance leads to chronic inflammation characterized by oxidative stress, pro-inflammatory cytokines and autoantibodies. |
| T7 | 770-940 | Sentence | denotes | Studies conducted in our laboratory have demonstrated the importance of this immune imbalance in causing hypertension in response to placental ischaemia in pregnant rats. |
| T8 | 941-1207 | Sentence | denotes | These studies confirm that increased CD4(+) T-cells and decreased Tregs during pregnancy leads to elevated inflammatory cytokines, endothelin (ET-1), reactive oxygen species (ROS) and agonistic autoantibodies to the angiotensin II (Ang II), type 1 receptor (AT1-AA). |
| T9 | 1208-1317 | Sentence | denotes | All of these factors taken together play an important role in increasing the blood pressure during pregnancy. |
| T10 | 1318-1506 | Sentence | denotes | Specifically, this review focuses on the decrease in Tregs, and their associated regulatory cytokine interleukin (IL)-10, which is seen in response to placental ischaemia during pregnancy. |
| T11 | 1507-1615 | Sentence | denotes | This study will also examine the effect of regulatory immune cell repopulation on the pathophysiology of PE. |
| T12 | 1616-1859 | Sentence | denotes | These studies show that restoring the balance of the immune system through increasing Tregs, either by adoptive transfer or by infusing IL-10, reduces the blood pressure and pathophysiology associated with placental ischaemia in pregnant rats. |
| T1 | 0-58 | Sentence | denotes | The role of inflammation in the pathology of preeclampsia. |
| T2 | 59-190 | Sentence | denotes | Preeclampsia (PE) affects 5-7% of all pregnancies in the United States and is the leading cause of maternal and prenatal morbidity. |
| T3 | 191-316 | Sentence | denotes | PE is associated with hypertension after week 20 of gestation, decreased renal function and small-for-gestational-age babies. |
| T4 | 317-393 | Sentence | denotes | Women with PE exhibit chronic inflammation and production of autoantibodies. |
| T5 | 394-642 | Sentence | denotes | It is hypothesized that during PE, placental ischaemia occurs as a result of shallow trophoblast invasion which is associated with an immune imbalance where pro-inflammatory CD4(+) T-cells are increased and T regulatory cells (Tregs) are decreased. |
| T6 | 643-769 | Sentence | denotes | This imbalance leads to chronic inflammation characterized by oxidative stress, pro-inflammatory cytokines and autoantibodies. |
| T7 | 770-940 | Sentence | denotes | Studies conducted in our laboratory have demonstrated the importance of this immune imbalance in causing hypertension in response to placental ischaemia in pregnant rats. |
| T8 | 941-1207 | Sentence | denotes | These studies confirm that increased CD4(+) T-cells and decreased Tregs during pregnancy leads to elevated inflammatory cytokines, endothelin (ET-1), reactive oxygen species (ROS) and agonistic autoantibodies to the angiotensin II (Ang II), type 1 receptor (AT1-AA). |
| T9 | 1208-1317 | Sentence | denotes | All of these factors taken together play an important role in increasing the blood pressure during pregnancy. |
| T10 | 1318-1506 | Sentence | denotes | Specifically, this review focuses on the decrease in Tregs, and their associated regulatory cytokine interleukin (IL)-10, which is seen in response to placental ischaemia during pregnancy. |
| T11 | 1507-1615 | Sentence | denotes | This study will also examine the effect of regulatory immune cell repopulation on the pathophysiology of PE. |
| T12 | 1616-1859 | Sentence | denotes | These studies show that restoring the balance of the immune system through increasing Tregs, either by adoptive transfer or by infusing IL-10, reduces the blood pressure and pathophysiology associated with placental ischaemia in pregnant rats. |
Preeclampsia
| Id | Subject | Object | Predicate | Lexical cue |
|---|---|---|---|---|
| PD-Preeclampsia-B_T1 | 45-57 | ORPHA:275555 | denotes | preeclampsia |
| PD-Preeclampsia-B_T2 | 59-71 | ORPHA:275555 | denotes | Preeclampsia |
Preeclampsia-compare
| Id | Subject | Object | Predicate | Lexical cue |
|---|---|---|---|---|
| PD-Preeclampsia-B_T1 | 45-57 | ORPHA:275555 | denotes | preeclampsia |
| PD-Preeclampsia-B_T2 | 59-71 | ORPHA:275555 | denotes | Preeclampsia |
sentences
| Id | Subject | Object | Predicate | Lexical cue |
|---|---|---|---|---|
| TextSentencer_T1 | 0-58 | Sentence | denotes | The role of inflammation in the pathology of preeclampsia. |
| TextSentencer_T2 | 59-190 | Sentence | denotes | Preeclampsia (PE) affects 5-7% of all pregnancies in the United States and is the leading cause of maternal and prenatal morbidity. |
| TextSentencer_T3 | 191-316 | Sentence | denotes | PE is associated with hypertension after week 20 of gestation, decreased renal function and small-for-gestational-age babies. |
| TextSentencer_T4 | 317-393 | Sentence | denotes | Women with PE exhibit chronic inflammation and production of autoantibodies. |
| TextSentencer_T5 | 394-642 | Sentence | denotes | It is hypothesized that during PE, placental ischaemia occurs as a result of shallow trophoblast invasion which is associated with an immune imbalance where pro-inflammatory CD4(+) T-cells are increased and T regulatory cells (Tregs) are decreased. |
| TextSentencer_T6 | 643-769 | Sentence | denotes | This imbalance leads to chronic inflammation characterized by oxidative stress, pro-inflammatory cytokines and autoantibodies. |
| TextSentencer_T7 | 770-940 | Sentence | denotes | Studies conducted in our laboratory have demonstrated the importance of this immune imbalance in causing hypertension in response to placental ischaemia in pregnant rats. |
| TextSentencer_T8 | 941-1207 | Sentence | denotes | These studies confirm that increased CD4(+) T-cells and decreased Tregs during pregnancy leads to elevated inflammatory cytokines, endothelin (ET-1), reactive oxygen species (ROS) and agonistic autoantibodies to the angiotensin II (Ang II), type 1 receptor (AT1-AA). |
| TextSentencer_T9 | 1208-1317 | Sentence | denotes | All of these factors taken together play an important role in increasing the blood pressure during pregnancy. |
| TextSentencer_T10 | 1318-1506 | Sentence | denotes | Specifically, this review focuses on the decrease in Tregs, and their associated regulatory cytokine interleukin (IL)-10, which is seen in response to placental ischaemia during pregnancy. |
| TextSentencer_T11 | 1507-1615 | Sentence | denotes | This study will also examine the effect of regulatory immune cell repopulation on the pathophysiology of PE. |
| TextSentencer_T12 | 1616-1859 | Sentence | denotes | These studies show that restoring the balance of the immune system through increasing Tregs, either by adoptive transfer or by infusing IL-10, reduces the blood pressure and pathophysiology associated with placental ischaemia in pregnant rats. |
| T1 | 0-58 | Sentence | denotes | The role of inflammation in the pathology of preeclampsia. |
| T2 | 59-190 | Sentence | denotes | Preeclampsia (PE) affects 5-7% of all pregnancies in the United States and is the leading cause of maternal and prenatal morbidity. |
| T3 | 191-316 | Sentence | denotes | PE is associated with hypertension after week 20 of gestation, decreased renal function and small-for-gestational-age babies. |
| T4 | 317-393 | Sentence | denotes | Women with PE exhibit chronic inflammation and production of autoantibodies. |
| T5 | 394-642 | Sentence | denotes | It is hypothesized that during PE, placental ischaemia occurs as a result of shallow trophoblast invasion which is associated with an immune imbalance where pro-inflammatory CD4(+) T-cells are increased and T regulatory cells (Tregs) are decreased. |
| T6 | 643-769 | Sentence | denotes | This imbalance leads to chronic inflammation characterized by oxidative stress, pro-inflammatory cytokines and autoantibodies. |
| T7 | 770-940 | Sentence | denotes | Studies conducted in our laboratory have demonstrated the importance of this immune imbalance in causing hypertension in response to placental ischaemia in pregnant rats. |
| T8 | 941-1207 | Sentence | denotes | These studies confirm that increased CD4(+) T-cells and decreased Tregs during pregnancy leads to elevated inflammatory cytokines, endothelin (ET-1), reactive oxygen species (ROS) and agonistic autoantibodies to the angiotensin II (Ang II), type 1 receptor (AT1-AA). |
| T9 | 1208-1317 | Sentence | denotes | All of these factors taken together play an important role in increasing the blood pressure during pregnancy. |
| T10 | 1318-1506 | Sentence | denotes | Specifically, this review focuses on the decrease in Tregs, and their associated regulatory cytokine interleukin (IL)-10, which is seen in response to placental ischaemia during pregnancy. |
| T11 | 1507-1615 | Sentence | denotes | This study will also examine the effect of regulatory immune cell repopulation on the pathophysiology of PE. |
| T12 | 1616-1859 | Sentence | denotes | These studies show that restoring the balance of the immune system through increasing Tregs, either by adoptive transfer or by infusing IL-10, reduces the blood pressure and pathophysiology associated with placental ischaemia in pregnant rats. |
UBERON-AE
| Id | Subject | Object | Predicate | Lexical cue |
|---|---|---|---|---|
| PD-UBERON-AE-B_T1 | 479-490 | http://purl.obolibrary.org/obo/UBERON_0000088 | denotes | trophoblast |
| PD-UBERON-AE-B_T2 | 1285-1290 | http://purl.obolibrary.org/obo/UBERON_0000178 | denotes | blood |
| PD-UBERON-AE-B_T3 | 1771-1776 | http://purl.obolibrary.org/obo/UBERON_0000178 | denotes | blood |
| PD-UBERON-AE-B_T4 | 1669-1682 | http://purl.obolibrary.org/obo/UBERON_0002405 | denotes | immune system |
performance-test
| Id | Subject | Object | Predicate | Lexical cue |
|---|---|---|---|---|
| PD-UBERON-AE-B_T1 | 1285-1290 | http://purl.obolibrary.org/obo/UBERON_0000178 | denotes | blood |
| PD-UBERON-AE-B_T2 | 1771-1776 | http://purl.obolibrary.org/obo/UBERON_0000178 | denotes | blood |
| PD-UBERON-AE-B_T3 | 429-438 | http://purl.obolibrary.org/obo/UBERON_0001987 | denotes | placental |
| PD-UBERON-AE-B_T4 | 903-912 | http://purl.obolibrary.org/obo/UBERON_0001987 | denotes | placental |
| PD-UBERON-AE-B_T5 | 1469-1478 | http://purl.obolibrary.org/obo/UBERON_0001987 | denotes | placental |
| PD-UBERON-AE-B_T6 | 1822-1831 | http://purl.obolibrary.org/obo/UBERON_0001987 | denotes | placental |
| PD-UBERON-AE-B_T7 | 479-490 | http://purl.obolibrary.org/obo/UBERON_0000088 | denotes | trophoblast |
| PD-UBERON-AE-B_T8 | 1669-1682 | http://purl.obolibrary.org/obo/UBERON_0002405 | denotes | immune system |