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- NCIT_C190644 IAO_0000115 "Human SLC16A2 wild-type allele is located in the vicinity of Xq13.2 and is approximately 112 kb in length. This allele, which encodes monocarboxylate transporter 8 protein, plays a role in cell uptake of thyroid hormone. Mutations in the gene are associated with Allan-Herndon-Dudley syndrome." @default.
- NCIT_C190644 NCIT_NHC0 "C190644" @default.
- NCIT_C190644 NCIT_P100 "300095" @default.
- NCIT_C190644 NCIT_P102 "NM_006517" @default.
- NCIT_C190644 NCIT_P106 "Gene or Genome" @default.
- NCIT_C190644 NCIT_P108 "SLC16A2 wt Allele" @default.
- NCIT_C190644 NCIT_P208 "CL1799117" @default.
- NCIT_C190644 NCIT_P321 "6567" @default.
- NCIT_C190644 NCIT_R37 NCIT_C17710 @default.
- NCIT_C190644 NCIT_R37 NCIT_C17828 @default.
- NCIT_C190644 NCIT_R37 NCIT_C18219 @default.
- NCIT_C190644 NCIT_R37 NCIT_C19143 @default.
- NCIT_C190644 NCIT_R37 NCIT_C19950 @default.
- NCIT_C190644 NCIT_R37 NCIT_C19986 @default.
- NCIT_C190644 NCIT_R37 NCIT_C20139 @default.
- NCIT_C190644 NCIT_R37 NCIT_C20480 @default.
- NCIT_C190644 NCIT_R37 NCIT_C21079 @default.
- NCIT_C190644 NCIT_R37 NCIT_C21124 @default.
- NCIT_C190644 NCIT_R37 NCIT_C28498 @default.
- NCIT_C190644 NCIT_R37 NCIT_C40792 @default.
- NCIT_C190644 NCIT_R37 NCIT_C41495 @default.
- NCIT_C190644 NCIT_R40 NCIT_C12219 @default.
- NCIT_C190644 NCIT_R40 NCIT_C13282 @default.
- NCIT_C190644 NCIT_R40 NCIT_C13377 @default.
- NCIT_C190644 NCIT_R40 NCIT_C13432 @default.
- NCIT_C190644 NCIT_R40 NCIT_C13446 @default.
- NCIT_C190644 NCIT_R40 NCIT_C14135 @default.
- NCIT_C190644 NCIT_R40 NCIT_C32221 @default.
- NCIT_C190644 NCIT_R40 NCIT_C34070 @default.
- NCIT_C190644 NCIT_R40 NCIT_C75596 @default.
- NCIT_C190644 NCIT_R41 NCIT_C14182 @default.
- NCIT_C190644 NCIT_R41 NCIT_C14225 @default.
- NCIT_C190644 NCIT_R41 NCIT_C14234 @default.
- NCIT_C190644 NCIT_R41 NCIT_C14250 @default.
- NCIT_C190644 NCIT_R41 NCIT_C14262 @default.
- NCIT_C190644 NCIT_R41 NCIT_C14282 @default.
- NCIT_C190644 NCIT_R41 NCIT_C25796 @default.
- NCIT_C190644 NCIT_R41 NCIT_C79740 @default.
- NCIT_C190644 normalizedInformationContent "95.413332725061409" @default.
- NCIT_C190644 referenceCount "2" @default.
- NCIT_C190644 hasExactSynonym "AHDS" @default.
- NCIT_C190644 hasExactSynonym "Allan-Herndon-Dudley Syndrome Gene" @default.
- NCIT_C190644 hasExactSynonym "DXS128" @default.
- NCIT_C190644 hasExactSynonym "DXS128E" @default.
- NCIT_C190644 hasExactSynonym "MCT 7" @default.
- NCIT_C190644 hasExactSynonym "MCT 8" @default.
- NCIT_C190644 hasExactSynonym "MCT7" @default.
- NCIT_C190644 hasExactSynonym "MCT8" @default.
- NCIT_C190644 hasExactSynonym "MRX22" @default.
- NCIT_C190644 hasExactSynonym "Mental Retardation, X-Linked 22 Gene" @default.
- NCIT_C190644 hasExactSynonym "SLC16A2 wt Allele" @default.
- NCIT_C190644 hasExactSynonym "Solute Carrier Family 16 (Monocarboxylic Acid Transporter), Member 2 Gene" @default.
- NCIT_C190644 hasExactSynonym "Solute Carrier Family 16 (Monocarboxylic Acid Transporters), Member 2 (Putative Transporter) Gene" @default.
- NCIT_C190644 hasExactSynonym "Solute Carrier Family 16 (Monocarboxylic Acid Transporters), Member 2 Gene" @default.
- NCIT_C190644 hasExactSynonym "Solute Carrier Family 16 Member 2 wt Allele" @default.
- NCIT_C190644 hasExactSynonym "Solute Carrier Family 16, Member 2 (Monocarboxylic Acid Transporter 8) Gene" @default.
- NCIT_C190644 hasExactSynonym "Solute Carrier Family 16, Member 2 (Thyroid Hormone Transporter) Gene" @default.
- NCIT_C190644 hasExactSynonym "XPCT" @default.
- NCIT_C190644 type Class @default.
- NCIT_C190644 isDefinedBy ncit.owl @default.
- NCIT_C190644 label "SLC16A2 wt Allele" @default.
- NCIT_C190644 subClassOf Ba26dfaa53c3c8d39c8d1ca5d73f230da @default.
- NCIT_C190644 subClassOf Be0ad67889d804247cccc78c387ef771c @default.
- NCIT_C190644 subClassOf NCIT_C16612 @default.
- NCIT_C190644 subClassOf NCIT_C190643 @default.
- NCIT_C190644 subClassOf NCIT_C190644 @default.
- NCIT_C190644 subClassOf NCIT_C21295 @default.
- NCIT_C190644 subClassOf NCIT_C28533 @default.