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Entity

Name
Alzheimer disease, familial, type 3
Namespace
MeSH
Namespace Version
20181007
Namespace URL
https://raw.githubusercontent.com/pharmacome/terminology/01c9daa61012b37dd0a1bc962521ba51a15b38f1/external/mesh-names.belns

Appears in Networks 1

In-Edges 1

p(HGNC:PSEN1) association path(MESH:"Alzheimer disease, familial, type 3") View Subject | View Object

It is well established that mutations in PS1 result in familial AD, and until recently it was thought that this was only due to alterations in APP processing. PubMed:24027553

Out-Edges 1

path(MESH:"Alzheimer disease, familial, type 3") association p(HGNC:PSEN1) View Subject | View Object

It is well established that mutations in PS1 result in familial AD, and until recently it was thought that this was only due to alterations in APP processing. PubMed:24027553

About

BEL Commons is developed and maintained in an academic capacity by Charles Tapley Hoyt and Daniel Domingo-Fernández at the Fraunhofer SCAI Department of Bioinformatics with support from the IMI project, AETIONOMY. It is built on top of PyBEL, an open source project. Please feel free to contact us here to give us feedback or report any issues. Also, see our Publishing Notes and Data Protection information.

If you find BEL Commons useful in your work, please consider citing: Hoyt, C. T., Domingo-Fernández, D., & Hofmann-Apitius, M. (2018). BEL Commons: an environment for exploration and analysis of networks encoded in Biological Expression Language. Database, 2018(3), 1–11.