An R object that contains associations between Disease Ontology terms and Human Entrez Genes. This data is first prepared based on http://sourceforge.net/p/diseaseontology/code/HEAD/tree/trunk/HumanDO.obo?format=raw and http://dga.nubic.northwestern.edu/ajax/Download.ajax.php, which results in annotations of Human Entrez Genes.
org.Hs.egDO <- dRDataLoader(RData = "org.Hs.egDO")
an object of class "GS", a list with following components:
set_info: a matrix of nSet X 4 containing gene set information, where nSet is the number of gene sets (i.e. DO terms), and the 4 columns are "setID" (i.e. "Term ID"), "name" (i.e. "Term Name"), "namespace" and "distance"
gs: a list of gene sets, each storing gene members thereof. Always, gene sets are identified by "setID" and gene members identified by "Entrez ID"
Schriml et al. (2012) Disease Ontology: a backbone for disease semantic integration. Nucleic Acids Res, 40:D940-946.
Peng et al. (2012) The Disease and Gene Annotations (DGA): an annotation resource for human disease. Nucleic Acids Res, 41:D553-560.
Sayers et al. (2011) Database resources of the National Center for Biotechnology Information. Nucleic Acids Res, 39:D38-51.
org.Hs.egDO <- dRDataLoader(RData='org.Hs.egDO')'org.Hs.egDO' (from https://github.com/hfang-bristol/RDataCentre/blob/master/dnet/1.0.7/org.Hs.egDO.RData?raw=true) has been loaded into the working environment (at 2018-01-19 12:38:14)names(org.Hs.egDO)[1] "gs" "set_info"