Matches in Ubergraph for { <http://purl.obolibrary.org/obo/NCIT_C75478> ?p ?o ?g. }
Showing items 1 to 29 of
29
with 100 items per page.
- NCIT_C75478 IAO_0000115 "A genetic syndrome caused by terminal 22q13 microdeletions. It is characterized by developmental delay and delayed or absent speech." @default.
- NCIT_C75478 NCIT_NHC0 "C75478" @default.
- NCIT_C75478 NCIT_P106 "Disease or Syndrome" @default.
- NCIT_C75478 NCIT_P108 "22q Telomere Deletion Syndrome" @default.
- NCIT_C75478 NCIT_P207 "C2699200" @default.
- NCIT_C75478 NCIT_P366 "Chromosome_22q_Telomere_Deletion_Syndrome" @default.
- NCIT_C75478 NCIT_R174 NCIT_C12219 @default.
- NCIT_C75478 NCIT_R174 NCIT_C13202 @default.
- NCIT_C75478 NCIT_R174 NCIT_C13203 @default.
- NCIT_C75478 NCIT_R174 NCIT_C13218 @default.
- NCIT_C75478 NCIT_R174 NCIT_C13404 @default.
- NCIT_C75478 NCIT_R174 NCIT_C14134 @default.
- NCIT_C75478 NCIT_R174 NCIT_C21599 @default.
- NCIT_C75478 normalizedInformationContent "100" @default.
- NCIT_C75478 referenceCount "1" @default.
- NCIT_C75478 hasExactSynonym "22q Telomere Deletion Syndrome" @default.
- NCIT_C75478 type Class @default.
- NCIT_C75478 isDefinedBy ncit.owl @default.
- NCIT_C75478 label "22q Telomere Deletion Syndrome" @default.
- NCIT_C75478 subClassOf B0a9b1a1ca197d2c40257f5b30cf3550b @default.
- NCIT_C75478 subClassOf B9c07b36d2e9611ba602b56f78d1026a9 @default.
- NCIT_C75478 subClassOf NCIT_C28193 @default.
- NCIT_C75478 subClassOf NCIT_C2991 @default.
- NCIT_C75478 subClassOf NCIT_C4873 @default.
- NCIT_C75478 subClassOf NCIT_C53529 @default.
- NCIT_C75478 subClassOf NCIT_C53543 @default.
- NCIT_C75478 subClassOf NCIT_C53547 @default.
- NCIT_C75478 subClassOf NCIT_C7057 @default.
- NCIT_C75478 subClassOf NCIT_C75478 @default.