Matches in Ubergraph for { <http://purl.obolibrary.org/obo/NCIT_C101757> ?p ?o ?g. }
Showing items 1 to 93 of
93
with 100 items per page.
- NCIT_C101757 IAO_0000115 "Human TTN wild-type allele is located in the vicinity of 2q31 and is approximately 305 kb in length. This allele, which encodes titin protein, is involved in both muscle filament structure and protein phosphorylation. Mutation of the gene is associated with hereditary myopathy with early respiratory failure, familial hypertrophic cardiomyopathy type 9, cardiomyopathy dilated type 1G, tardive tibial muscular dystrophy, limb-girdle muscular dystrophy type 2J and early-onset myopathy with fatal cardiomyopathy." @default.
- NCIT_C101757 NCIT_NHC0 "C101757" @default.
- NCIT_C101757 NCIT_P100 "188840" @default.
- NCIT_C101757 NCIT_P102 "X90568" @default.
- NCIT_C101757 NCIT_P106 "Gene or Genome" @default.
- NCIT_C101757 NCIT_P108 "TTN wt Allele" @default.
- NCIT_C101757 NCIT_P207 "C3538714" @default.
- NCIT_C101757 NCIT_P321 "7273" @default.
- NCIT_C101757 NCIT_R130 NCIT_C20633 @default.
- NCIT_C101757 NCIT_R130 NCIT_C39701 @default.
- NCIT_C101757 NCIT_R130 NCIT_C91470 @default.
- NCIT_C101757 NCIT_R130 NCIT_C91484 @default.
- NCIT_C101757 NCIT_R37 NCIT_C16983 @default.
- NCIT_C101757 NCIT_R37 NCIT_C17019 @default.
- NCIT_C101757 NCIT_R37 NCIT_C17133 @default.
- NCIT_C101757 NCIT_R37 NCIT_C17710 @default.
- NCIT_C101757 NCIT_R37 NCIT_C17828 @default.
- NCIT_C101757 NCIT_R37 NCIT_C18100 @default.
- NCIT_C101757 NCIT_R37 NCIT_C18496 @default.
- NCIT_C101757 NCIT_R37 NCIT_C18839 @default.
- NCIT_C101757 NCIT_R37 NCIT_C19395 @default.
- NCIT_C101757 NCIT_R37 NCIT_C19406 @default.
- NCIT_C101757 NCIT_R37 NCIT_C19536 @default.
- NCIT_C101757 NCIT_R37 NCIT_C19899 @default.
- NCIT_C101757 NCIT_R37 NCIT_C19903 @default.
- NCIT_C101757 NCIT_R37 NCIT_C19988 @default.
- NCIT_C101757 NCIT_R37 NCIT_C20480 @default.
- NCIT_C101757 NCIT_R37 NCIT_C20679 @default.
- NCIT_C101757 NCIT_R37 NCIT_C20748 @default.
- NCIT_C101757 NCIT_R37 NCIT_C21045 @default.
- NCIT_C101757 NCIT_R37 NCIT_C21124 @default.
- NCIT_C101757 NCIT_R37 NCIT_C21128 @default.
- NCIT_C101757 NCIT_R37 NCIT_C21147 @default.
- NCIT_C101757 NCIT_R37 NCIT_C21198 @default.
- NCIT_C101757 NCIT_R37 NCIT_C28498 @default.
- NCIT_C101757 NCIT_R37 NCIT_C30085 @default.
- NCIT_C101757 NCIT_R37 NCIT_C40795 @default.
- NCIT_C101757 NCIT_R37 NCIT_C40800 @default.
- NCIT_C101757 NCIT_R37 NCIT_C40854 @default.
- NCIT_C101757 NCIT_R37 NCIT_C41480 @default.
- NCIT_C101757 NCIT_R37 NCIT_C41517 @default.
- NCIT_C101757 NCIT_R40 NCIT_C12219 @default.
- NCIT_C101757 NCIT_R40 NCIT_C13282 @default.
- NCIT_C101757 NCIT_R40 NCIT_C13377 @default.
- NCIT_C101757 NCIT_R40 NCIT_C13432 @default.
- NCIT_C101757 NCIT_R40 NCIT_C13446 @default.
- NCIT_C101757 NCIT_R40 NCIT_C14135 @default.
- NCIT_C101757 NCIT_R40 NCIT_C32221 @default.
- NCIT_C101757 NCIT_R40 NCIT_C34070 @default.
- NCIT_C101757 NCIT_R40 NCIT_C54239 @default.
- NCIT_C101757 NCIT_R41 NCIT_C14182 @default.
- NCIT_C101757 NCIT_R41 NCIT_C14225 @default.
- NCIT_C101757 NCIT_R41 NCIT_C14234 @default.
- NCIT_C101757 NCIT_R41 NCIT_C14250 @default.
- NCIT_C101757 NCIT_R41 NCIT_C14262 @default.
- NCIT_C101757 NCIT_R41 NCIT_C14282 @default.
- NCIT_C101757 NCIT_R41 NCIT_C25796 @default.
- NCIT_C101757 NCIT_R41 NCIT_C79740 @default.
- NCIT_C101757 normalizedInformationContent "100" @default.
- NCIT_C101757 referenceCount "1" @default.
- NCIT_C101757 hasExactSynonym "CMD1G" @default.
- NCIT_C101757 hasExactSynonym "CMH9" @default.
- NCIT_C101757 hasExactSynonym "CMPD4" @default.
- NCIT_C101757 hasExactSynonym "Cardiomyopathy, Dilated 1G (Autosomal Dominant) Gene" @default.
- NCIT_C101757 hasExactSynonym "DKFZp451N061" @default.
- NCIT_C101757 hasExactSynonym "EOMFC" @default.
- NCIT_C101757 hasExactSynonym "FLJ26020" @default.
- NCIT_C101757 hasExactSynonym "FLJ26409" @default.
- NCIT_C101757 hasExactSynonym "FLJ32040" @default.
- NCIT_C101757 hasExactSynonym "FLJ34413" @default.
- NCIT_C101757 hasExactSynonym "FLJ39564" @default.
- NCIT_C101757 hasExactSynonym "FLJ43066" @default.
- NCIT_C101757 hasExactSynonym "HMERF" @default.
- NCIT_C101757 hasExactSynonym "LGMD2J" @default.
- NCIT_C101757 hasExactSynonym "MYLK5" @default.
- NCIT_C101757 hasExactSynonym "TMD" @default.
- NCIT_C101757 hasExactSynonym "TTN wt Allele" @default.
- NCIT_C101757 hasExactSynonym "Titin wt Allele" @default.
- NCIT_C101757 type Class @default.
- NCIT_C101757 isDefinedBy ncit.owl @default.
- NCIT_C101757 label "TTN wt Allele" @default.
- NCIT_C101757 subClassOf NCIT_C101756 @default.
- NCIT_C101757 subClassOf NCIT_C101757 @default.
- NCIT_C101757 subClassOf NCIT_C16612 @default.
- NCIT_C101757 subClassOf NCIT_C20744 @default.
- NCIT_C101757 subClassOf NCIT_C20745 @default.
- NCIT_C101757 subClassOf NCIT_C21281 @default.
- NCIT_C101757 subClassOf NCIT_C25870 @default.
- NCIT_C101757 subClassOf NCIT_C25871 @default.
- NCIT_C101757 subClassOf NCIT_C25872 @default.
- NCIT_C101757 subClassOf NCIT_C25873 @default.
- NCIT_C101757 equivalentClass B9c9ca6e7c5e44cecfabbfcede14a0122 @default.
- NCIT_C101757 equivalentClass Bb1cc2e3a02d99efe6168f0cdfa1fb50a @default.