Matches in Ubergraph for { <http://purl.obolibrary.org/obo/NCIT_C74974> ?p ?o ?g. }
Showing items 1 to 65 of
65
with 100 items per page.
- NCIT_C74974 IAO_0000115 "Human ATP7A wild-type allele is located within Xq13.2-q13.3 and is approximately 139 kb in length. This allele, which encodes copper-transporting ATPase 1 protein, plays a role in the localization of copper ions. Mutations in the gene are associated with both Menkes disease and occipital horn syndrome." @default.
- NCIT_C74974 NCIT_NHC0 "C74974" @default.
- NCIT_C74974 NCIT_P100 "300011" @default.
- NCIT_C74974 NCIT_P102 "L06133" @default.
- NCIT_C74974 NCIT_P106 "Gene or Genome" @default.
- NCIT_C74974 NCIT_P107 "ATP7A wt Allele" @default.
- NCIT_C74974 NCIT_P108 "ATP7A wt Allele" @default.
- NCIT_C74974 NCIT_P207 "C2699122" @default.
- NCIT_C74974 NCIT_P321 "538" @default.
- NCIT_C74974 NCIT_P322 "CTRP" @default.
- NCIT_C74974 NCIT_P366 "ATP7A_wt_Allele" @default.
- NCIT_C74974 NCIT_R37 NCIT_C16702 @default.
- NCIT_C74974 NCIT_R37 NCIT_C17710 @default.
- NCIT_C74974 NCIT_R37 NCIT_C17828 @default.
- NCIT_C74974 NCIT_R37 NCIT_C18219 @default.
- NCIT_C74974 NCIT_R37 NCIT_C19403 @default.
- NCIT_C74974 NCIT_R37 NCIT_C19536 @default.
- NCIT_C74974 NCIT_R37 NCIT_C19899 @default.
- NCIT_C74974 NCIT_R37 NCIT_C19939 @default.
- NCIT_C74974 NCIT_R37 NCIT_C19950 @default.
- NCIT_C74974 NCIT_R37 NCIT_C19986 @default.
- NCIT_C74974 NCIT_R37 NCIT_C20139 @default.
- NCIT_C74974 NCIT_R37 NCIT_C20480 @default.
- NCIT_C74974 NCIT_R37 NCIT_C21079 @default.
- NCIT_C74974 NCIT_R37 NCIT_C21198 @default.
- NCIT_C74974 NCIT_R37 NCIT_C28498 @default.
- NCIT_C74974 NCIT_R37 NCIT_C40515 @default.
- NCIT_C74974 NCIT_R37 NCIT_C40792 @default.
- NCIT_C74974 NCIT_R41 NCIT_C14182 @default.
- NCIT_C74974 NCIT_R41 NCIT_C14225 @default.
- NCIT_C74974 NCIT_R41 NCIT_C14234 @default.
- NCIT_C74974 NCIT_R41 NCIT_C14250 @default.
- NCIT_C74974 NCIT_R41 NCIT_C14262 @default.
- NCIT_C74974 NCIT_R41 NCIT_C14282 @default.
- NCIT_C74974 NCIT_R41 NCIT_C25796 @default.
- NCIT_C74974 NCIT_R41 NCIT_C79740 @default.
- NCIT_C74974 normalizedInformationContent "100" @default.
- NCIT_C74974 referenceCount "1" @default.
- NCIT_C74974 hasExactSynonym "ATP7A wt Allele" @default.
- NCIT_C74974 hasExactSynonym "ATPase, Cu(2+)-Transporting, Alpha Polypeptide Gene" @default.
- NCIT_C74974 hasExactSynonym "ATPase, Cu++ Transporting, Alpha Polypeptide (Menkes Syndrome) Gene" @default.
- NCIT_C74974 hasExactSynonym "ATPase, Cu++ Transporting, Alpha Polypeptide wt Allele" @default.
- NCIT_C74974 hasExactSynonym "DSMAX" @default.
- NCIT_C74974 hasExactSynonym "FLJ17790" @default.
- NCIT_C74974 hasExactSynonym "MC1" @default.
- NCIT_C74974 hasExactSynonym "MK" @default.
- NCIT_C74974 hasExactSynonym "MNK" @default.
- NCIT_C74974 hasExactSynonym "Menkes Syndrome Gene" @default.
- NCIT_C74974 hasExactSynonym "RP3-465G10.1" @default.
- NCIT_C74974 hasExactSynonym "SMAX3" @default.
- NCIT_C74974 inSubset NCIT_C116977 @default.
- NCIT_C74974 inSubset NCIT_C142799 @default.
- NCIT_C74974 inSubset NCIT_C142800 @default.
- NCIT_C74974 type Class @default.
- NCIT_C74974 isDefinedBy ncit.owl @default.
- NCIT_C74974 label "ATP7A wt Allele" @default.
- NCIT_C74974 subClassOf B07513a889b954e4701eb93471508145b @default.
- NCIT_C74974 subClassOf B44c4acc3455eaa912f4c2dd6f36618ee @default.
- NCIT_C74974 subClassOf NCIT_C158414 @default.
- NCIT_C74974 subClassOf NCIT_C16612 @default.
- NCIT_C74974 subClassOf NCIT_C21281 @default.
- NCIT_C74974 subClassOf NCIT_C21295 @default.
- NCIT_C74974 subClassOf NCIT_C28533 @default.
- NCIT_C74974 subClassOf NCIT_C74973 @default.
- NCIT_C74974 subClassOf NCIT_C74974 @default.