An R object that contains associations between HPCM terms and Human Entrez Genes. This data is first prepared based on http://purl.obolibrary.org/obo/hp.obo and http://compbio.charite.de/hudson/job/hpo.annotations.monthly/lastStableBuild/artifact/annotation/ALL_SOURCES_ALL_FREQUENCIES_genes_to_phenotype.txt.
org.Hs.egHPCM <- dRDataLoader(RData = "org.Hs.egHPCM")
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. HPCM 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"
Robinson et al. (2012) The Human Phenotype Ontology: a tool for annotating and analyzing human hereditary disease. Am J Hum Genet, 83:610-615.
org.Hs.egHPCM <- dRDataLoader(RData='org.Hs.egHPCM')'org.Hs.egHPCM' (from https://github.com/hfang-bristol/RDataCentre/blob/master/dnet/1.0.7/org.Hs.egHPCM.RData?raw=true) has been loaded into the working environment (at 2018-01-19 12:38:19)names(org.Hs.egHPCM)[1] "gs" "set_info"