Matches in Ubergraph for { <http://purl.obolibrary.org/obo/NCIT_C191426> ?p ?o ?g. }
Showing items 1 to 58 of
58
with 100 items per page.
- NCIT_C191426 IAO_0000115 "Human PMM2 wild-type allele is located in the vicinity of 16p13.2 and is approximately 74 kb in length. This allele, which encodes phosphomannomutase 2 protein, plays a role in the synthesis of nucleotide sugars. Mutation of the gene is associated with congenital disorder of glycosylation 1a." @default.
- NCIT_C191426 NCIT_NHC0 "C191426" @default.
- NCIT_C191426 NCIT_P100 "601785" @default.
- NCIT_C191426 NCIT_P102 "BC008310" @default.
- NCIT_C191426 NCIT_P106 "Gene or Genome" @default.
- NCIT_C191426 NCIT_P108 "PMM2 wt Allele" @default.
- NCIT_C191426 NCIT_P208 "CL1905056" @default.
- NCIT_C191426 NCIT_P321 "5373" @default.
- NCIT_C191426 NCIT_R130 NCIT_C18611 @default.
- NCIT_C191426 NCIT_R130 NCIT_C20633 @default.
- NCIT_C191426 NCIT_R130 NCIT_C38810 @default.
- NCIT_C191426 NCIT_R130 NCIT_C38840 @default.
- NCIT_C191426 NCIT_R130 NCIT_C39726 @default.
- NCIT_C191426 NCIT_R37 NCIT_C16643 @default.
- NCIT_C191426 NCIT_R37 NCIT_C17019 @default.
- NCIT_C191426 NCIT_R37 NCIT_C17710 @default.
- NCIT_C191426 NCIT_R37 NCIT_C17828 @default.
- NCIT_C191426 NCIT_R37 NCIT_C17933 @default.
- NCIT_C191426 NCIT_R37 NCIT_C19406 @default.
- NCIT_C191426 NCIT_R37 NCIT_C19536 @default.
- NCIT_C191426 NCIT_R37 NCIT_C19899 @default.
- NCIT_C191426 NCIT_R37 NCIT_C19903 @default.
- NCIT_C191426 NCIT_R37 NCIT_C21034 @default.
- NCIT_C191426 NCIT_R37 NCIT_C21198 @default.
- NCIT_C191426 NCIT_R37 NCIT_C28498 @default.
- NCIT_C191426 NCIT_R41 NCIT_C14182 @default.
- NCIT_C191426 NCIT_R41 NCIT_C14225 @default.
- NCIT_C191426 NCIT_R41 NCIT_C14234 @default.
- NCIT_C191426 NCIT_R41 NCIT_C14250 @default.
- NCIT_C191426 NCIT_R41 NCIT_C14262 @default.
- NCIT_C191426 NCIT_R41 NCIT_C14282 @default.
- NCIT_C191426 NCIT_R41 NCIT_C25796 @default.
- NCIT_C191426 NCIT_R41 NCIT_C79740 @default.
- NCIT_C191426 normalizedInformationContent "100" @default.
- NCIT_C191426 referenceCount "1" @default.
- NCIT_C191426 hasExactSynonym "CDG1" @default.
- NCIT_C191426 hasExactSynonym "CDG1a" @default.
- NCIT_C191426 hasExactSynonym "CDGS" @default.
- NCIT_C191426 hasExactSynonym "Congenital Disorder of Glycosylation, Type Ia Gene" @default.
- NCIT_C191426 hasExactSynonym "Mannose-6-Phosphate Isomerase Gene" @default.
- NCIT_C191426 hasExactSynonym "PMI" @default.
- NCIT_C191426 hasExactSynonym "PMI1" @default.
- NCIT_C191426 hasExactSynonym "PMM 2" @default.
- NCIT_C191426 hasExactSynonym "PMM2 wt Allele" @default.
- NCIT_C191426 hasExactSynonym "Phosphomannomutase 2 wt Allele" @default.
- NCIT_C191426 hasExactSynonym "Phosphomannose Isomerase 1 Gene" @default.
- NCIT_C191426 type Class @default.
- NCIT_C191426 isDefinedBy ncit.owl @default.
- NCIT_C191426 label "PMM2 wt Allele" @default.
- NCIT_C191426 subClassOf B2ef71495e3b7c7d04ebdbf9e8f95d59a @default.
- NCIT_C191426 subClassOf B5a676e7bfba688113c1a3c6238c74334 @default.
- NCIT_C191426 subClassOf B68cc3cccca3e43ab6b69bbc386a83dee @default.
- NCIT_C191426 subClassOf Ba8348ffaad63a97311505ed3147c79ee @default.
- NCIT_C191426 subClassOf NCIT_C16612 @default.
- NCIT_C191426 subClassOf NCIT_C191424 @default.
- NCIT_C191426 subClassOf NCIT_C191426 @default.
- NCIT_C191426 subClassOf NCIT_C21281 @default.
- NCIT_C191426 subClassOf NCIT_C25941 @default.