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Matches in Ubergraph for { <http://purl.obolibrary.org/obo/NCIT_C7930> ?p ?o ?g. }

• NCIT_C7930 IAO_0000115 "An angiocentric and angiodestructive lymphoproliferative disease involving extranodal sites, comprised of Epstein-Barr virus (EBV)-positive B-cells admixed with reactive T-cells. Incidence is higher among adult males; patients with a history of immunodeficiency are at increased risk. The most common site of involvement is the lung; other common sites include brain, kidney, liver, and skin. Morphologically, three grades are recognized: grade I, II, and III. Grade III lymphomatoid granulomatosis should be approached clinically as a subtype of diffuse large B-cell lymphoma." @default.
• NCIT_C7930 NCIT_A32 NCIT_C176985 @default.
• NCIT_C7930 NCIT_A32 NCIT_C177621 @default.
• NCIT_C7930 NCIT_NHC0 "C7930" @default.
• NCIT_C7930 NCIT_P106 "Neoplastic Process" @default.
• NCIT_C7930 NCIT_P108 "Lymphomatoid Granulomatosis" @default.
• NCIT_C7930 NCIT_P207 "C0024307" @default.
• NCIT_C7930 NCIT_P322 "CTEP" @default.
• NCIT_C7930 NCIT_P322 "GDC" @default.
• NCIT_C7930 NCIT_P325 "Destructive growth of lymph cells, usually involving the lungs, skin, kidneys, and central nervous system. Grades I and II are not considered cancerous, but grade III is considered a lymphoma." @default.
• NCIT_C7930 NCIT_P334 "9766/1" @default.
• NCIT_C7930 NCIT_P363 "Uncertain Malignant Potential" @default.
• NCIT_C7930 NCIT_P366 "Lymphomatoid_Granulomatosis" @default.
• NCIT_C7930 NCIT_P375 "9766/1" @default.
• NCIT_C7930 NCIT_P375 "Lymphomatoid granulomatosis" @default.
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