Matches in Ubergraph for { <http://purl.obolibrary.org/obo/NCIT_C157579> ?p ?o ?g. }
Showing items 1 to 32 of
32
with 100 items per page.
- NCIT_C157579 IAO_0000115 "A change in the nucleotide sequence of the MAGT1 gene." @default.
- NCIT_C157579 NCIT_NHC0 "C157579" @default.
- NCIT_C157579 NCIT_P106 "Cell or Molecular Dysfunction" @default.
- NCIT_C157579 NCIT_P107 "MAGT1 Gene Mutation" @default.
- NCIT_C157579 NCIT_P108 "MAGT1 Gene Mutation" @default.
- NCIT_C157579 NCIT_P208 "CL937280" @default.
- NCIT_C157579 NCIT_P322 "CTRP" @default.
- NCIT_C157579 NCIT_R177 NCIT_C157561 @default.
- NCIT_C157579 NCIT_R177 NCIT_C16612 @default.
- NCIT_C157579 NCIT_R177 NCIT_C21295 @default.
- NCIT_C157579 NCIT_R177 NCIT_C28533 @default.
- NCIT_C157579 normalizedInformationContent "100" @default.
- NCIT_C157579 referenceCount "1" @default.
- NCIT_C157579 hasExactSynonym "IAP Gene Mutation" @default.
- NCIT_C157579 hasExactSynonym "MAGT1 Gene Mutation" @default.
- NCIT_C157579 hasExactSynonym "MagT1 Mutation" @default.
- NCIT_C157579 hasExactSynonym "Magnesium Transporter 1 Gene Mutation" @default.
- NCIT_C157579 hasExactSynonym "OST3B Gene Mutation" @default.
- NCIT_C157579 hasExactSynonym "XMEN Gene Mutation" @default.
- NCIT_C157579 inSubset NCIT_C116977 @default.
- NCIT_C157579 inSubset NCIT_C142799 @default.
- NCIT_C157579 inSubset NCIT_C142800 @default.
- NCIT_C157579 type Class @default.
- NCIT_C157579 isDefinedBy ncit.owl @default.
- NCIT_C157579 label "MAGT1 Gene Mutation" @default.
- NCIT_C157579 subClassOf B143e7c9216b01f1dde20ac6657f6c734 @default.
- NCIT_C157579 subClassOf B18f9c8b62e92c26a623e7dc5e1e5c45a @default.
- NCIT_C157579 subClassOf NCIT_C157579 @default.
- NCIT_C157579 subClassOf NCIT_C36391 @default.
- NCIT_C157579 subClassOf NCIT_C3910 @default.
- NCIT_C157579 subClassOf NCIT_C97926 @default.
- NCIT_C157579 subClassOf NCIT_C97927 @default.