Knowledge graph · Trial
Frequency and Clinical Phenotype of BAP1 Hereditary Predisposition Syndrome
RECRUITING
- Identifier
- CI-TRIAL-00104946
- Entity page
- /trial/NCT04792463 ↗
- Edges
- 6
- Neighbours
- 6 cancers
- Drawn
- 6 of 6 neighbours (cap 60); table lists every fetched edge
Accepted: cancer:<slug>, gene:<symbol>, variant:<slug>, drug:<slug>, trial:<NCT id>, or a bare CI id. Find slugs with search.
Most connectedLung Non-Small Cell Carcinoma 3,149Malignant Colorectal Neoplasm 1,866ABL1 298EGFR 276Imatinib 450Dasatinib 321
Neighbourhood
Radial view
Focus at the centre; neighbours grouped by entity type. Click a node to re-centre the graph on it; ↗ opens the entity page. Hover a spoke for relationship, evidence level, cancer context and source.
Edges
Every edge, grouped by relationship
Source-native edges first (aggregated per neighbour, direction, evidence level and source), then derived registry links. Up to 15 per relationship (10 trials); “show all” raises one group to 200.
| Relationship | Neighbour | Direction | Evidence level | Cancer context | Support | Claim | Source | Expand |
|---|---|---|---|---|---|---|---|---|
| Frequency and Clinical Phenotype of BAP1 Hereditary Predisposition Syndrome condition of …CONDITION_OFderived6 of 6 | ||||||||
| ← condition of | Cholangiocarcinoma registry condition “Cholangiocarcinoma” mapped ONTOLOGY_EXACT | — | — | Cholangiocarcinoma | 1 | Observed | clinicaltrials | graph → |
| ← condition of | Cutaneous Melanoma registry condition “Cutaneous Melanoma” mapped ONTOLOGY_EXACT | — | — | |||||