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- B1c4f25a966236f3a6407cc6ee46deca5 hasDbXref "NCIT:C4835" @default.
- B1c4f25a966236f3a6407cc6ee46deca5 type Axiom @default.
- B1c4f25a966236f3a6407cc6ee46deca5 annotatedProperty IAO_0000115 @default.
- B1c4f25a966236f3a6407cc6ee46deca5 annotatedSource MONDO_0002625 @default.
- B1c4f25a966236f3a6407cc6ee46deca5 annotatedTarget "A small round cell bone tumor that lacks morphologic, immunohistochemical, and electron microscopic evidence of neuroectodermal differentiation. It represents one of the two ends of the spectrum called Ewing sarcoma/peripheral neuroectodermal tumor. It often affects the diaphysis or metaphyseal-diaphyseal portion of long bones. Clinical findings include pain and a mass in the involved area. fever, anemia, leukocytosis, and an increased sedimentation rate are often seen. X-ray examination reveals osteolytic lesions. The prognosis depends on the stage, anatomic location, and size of the tumor." @default.