From: <pr...@us...> - 2012-07-15 13:29:03
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Revision: 4400 http://obo.svn.sourceforge.net/obo/?rev=4400&view=rev Author: probins Date: 2012-07-15 13:28:57 +0000 (Sun, 15 Jul 2012) Log Message: ----------- Removing 159552, it is a gene entry without a Mendelian disease Removed Paths: ------------- phenotype-commons/annotations/OMIM/by-disease/annotated/OMIM-159552.tab Deleted: phenotype-commons/annotations/OMIM/by-disease/annotated/OMIM-159552.tab =================================================================== --- phenotype-commons/annotations/OMIM/by-disease/annotated/OMIM-159552.tab 2012-07-15 08:30:52 UTC (rev 4399) +++ phenotype-commons/annotations/OMIM/by-disease/annotated/OMIM-159552.tab 2012-07-15 13:28:57 UTC (rev 4400) @@ -1,3 +0,0 @@ -Disease ID Disease Name Gene ID Gene Name Genotype Gene Symbol(s) Phenotype ID Phenotype Name Age of Onset ID Age of Onset Name Evidence ID Evidence Name Frequency Sex ID Sex Name Negation ID Negation Name Description Pub Assigned by Date Created -OMIM:159552 MYELOID CELL LEUKEMIA 1 HP:0000006 Autosomal dominant inheritance IEA IEA OMIM:159552 HPO 17.02.2009 -OMIM:159552 MYELOID CELL LEUKEMIA 1 HP:0005519 Myeloid cell leukemia 1 IEA IEA OMIM:159552 HPO 17.02.2009 This was sent by the SourceForge.net collaborative development platform, the world's largest Open Source development site. |