Terminology Service < Semantic Lookup Platform

All terms in NCIT

Label	Id	Description
Gibi	NCIT_C68571	[A prefix used in binary numeral system for denoting a quantity of two raised to the power of 30, which is equal to 1 073 741 824.]
Tebi	NCIT_C68572	[A prefix used in binary numeral system for denoting a quantity of two raised to the power of 40, which is equal to 1 099 511 627 776.]
Pebi	NCIT_C68573	[A prefix used in binary numeral system for denoting a quantity of two raised to the power of 50, which is equal to 1 125 899 906 842 624.]
Exbi	NCIT_C68574	[A prefix used in binary numeral system for denoting a quantity of two raised to the power of 60, which is equal to 1 152 921 504 606 846 976.]
OLIG2 Gene	NCIT_C68575	[This gene is involved in transcriptional regulation and oligodendrocyte and motor neuron differentiation. This gene may play a role in the development of brain tumors.]
Acute Adult T-Cell Leukemia/Lymphoma	NCIT_C36265	[The most common variant of adult T-cell leukemia/lymphoma. It is characterized by systemic disease with a leukemic phase, generalized lymphadenopathy, and skin lesions. Hypercalcemia is commonly seen. -- 2004]
Blinding Schema Code	NCIT_C93520	[A coded value specifying the type of blinding that is used for the trial.]
OLIG2 wt Allele	NCIT_C68576	[Human OLIG2 wild-type allele is located in the vicinity of 21q22.11 and is approximately 3 kb in length. This allele, which encodes oligodendrocyte transcription factor 2 protein, is involved in neuronal progenitor cell fate determination. The wild-type allele is expressed in oligodendroglial tumors and is involved in a chromosomal translocation t(14;21)(q11.2;q22), which is associated with T-cell acute lymphoblastic leukemia.]
21q22.11	NCIT_C25021	[A chromosome band present on 21q]
Oligodendrocyte Transcription Factor 2	NCIT_C68577	[Oligodendrocyte transcription factor 2 (323 aa, ~32 kDa) is encoded by the human OLIG2 gene. This protein plays a role in the differentiation of oligodendrocytes and motor neurons.]
bHLH Domain	NCIT_C13450	[The bHLH domain is a bipartite DNA-binding domain containing a basic region upstream of an amphipathic helix-loop-helix region. The basic region interacts with DNA and the HLH motif mediates protein dimerization.]
Breed Code	NCIT_C93523	[A coded value specifying a group of animals presumably related by descent from common ancestors and visibly similar in most characteristics.]
Category Code	NCIT_C93524	[A coded value specifying a classification.]
Text	NCIT_C25704	[The words of something written.]
MBL2 Gene	NCIT_C68578	[This gene is involved in the complement immune response pathway.]
MBL2 wt Allele	NCIT_C68579	[Human MBL2 wild-type allele is located within 10q11.2-q21 and is approximately 6 kb in length. This allele, which encodes mannose-binding protein C, is involved in pathogen immune response initiation through activation of the complement pathway. Polymorphisms in the allele may increase the risk for colon cancer.]
Mannose-Binding Protein C	NCIT_C68581	[Mannose-binding protein C (248 aa, ~26 kDa) is encoded by the human MBL2 gene. This protein plays a role in the initiation of targeted host defense mechanisms against pathogens by activating the complement pathway.]
NEDD4 Gene	NCIT_C68582	[This gene may play a role in viral infection and tumor suppression.]
NEDD4 wt Allele	NCIT_C68583	[Human NEDD4 wild-type allele is located in the vicinity of 15q and is approximately 167 kb in length. This allele, which encodes E3 ubiquitin-protein ligase NEDD4 protein, may be involved in viral replication progression.]
15p	NCIT_C13540	[Proximal (short) arm of chromosome 15]