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[Obo-svn-commit] SF.net SVN: obo:[4117] phenotype-commons/annotations/OMIM/by-disease
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From: <pr...@us...> - 2011-12-31 11:41:49
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Revision: 4117
http://obo.svn.sourceforge.net/obo/?rev=4117&view=rev
Author: probins
Date: 2011-12-31 11:41:42 +0000 (Sat, 31 Dec 2011)
Log Message:
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Adding new annoptations to annotated folder
Modified Paths:
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phenotype-commons/annotations/OMIM/by-disease/MIM-606966.tab
Added Paths:
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phenotype-commons/annotations/OMIM/by-disease/annotated/MIM-136800.tab
phenotype-commons/annotations/OMIM/by-disease/annotated/MIM-211410.tab
phenotype-commons/annotations/OMIM/by-disease/annotated/MIM-211420.tab
phenotype-commons/annotations/OMIM/by-disease/annotated/MIM-278800.tab
phenotype-commons/annotations/OMIM/by-disease/annotated/MIM-606966.tab
Modified: phenotype-commons/annotations/OMIM/by-disease/MIM-606966.tab
===================================================================
--- phenotype-commons/annotations/OMIM/by-disease/MIM-606966.tab 2011-12-28 15:50:57 UTC (rev 4116)
+++ phenotype-commons/annotations/OMIM/by-disease/MIM-606966.tab 2011-12-31 11:41:42 UTC (rev 4117)
@@ -7,4 +7,5 @@
MIM:606966 NEPHRONOPHTHISIS 4 MIM:607215 NPHP4 HP:0001903 IEA 17.02.2009
MIM:606966 NEPHRONOPHTHISIS 4 MIM:607215 NPHP4 HP:0001959 GO:0042756 PATO:0000912 IEA 17.02.2009
MIM:606966 NEPHRONOPHTHISIS 4 MIM:607215 NPHP4 HP:0003774 IEA 17.02.2009
-MIM:606966 NEPHRONOPHTHISIS 4 MIM:607215 NPHP4 HP:0005578 IEA 17.02.2009
+MIM:606966 NEPHRONOPHTHISIS 4 MIM:607215 NPHP4 HP:0000108 IEA 31.12.2011
+MIM:606966 NEPHRONOPHTHISIS 4 MIM:607215 NPHP4 HP:0000092 IEA 31.12.2011
Added: phenotype-commons/annotations/OMIM/by-disease/annotated/MIM-136800.tab
===================================================================
--- phenotype-commons/annotations/OMIM/by-disease/annotated/MIM-136800.tab (rev 0)
+++ phenotype-commons/annotations/OMIM/by-disease/annotated/MIM-136800.tab 2011-12-31 11:41:42 UTC (rev 4117)
@@ -0,0 +1,5 @@
+Disease ID Disease Name Gene ID Gene Name Genotype Gene Symbol(s) Phenotype ID Phenotype Name Entity ID Entity Name Quality ID Quality Name Add'l Entity ID Add'l Entity Name Age of Onset ID Age of Onset Name Evidence Frequency Abnormal ID Abnormal Name Sex Negation ID Negation Name Description Orthologs Pub Date Created
+MIM:136800 CORNEAL DYSTROPHY, FUCHS ENDOTHELIAL, 1 MIM:120252 COLLAGEN, TYPE VIII, ALPHA-2 COL8A2 HP:0000006 Autosomal dominant inheritance IEA Feb 17, 2009
+MIM:136800 CORNEAL DYSTROPHY, FUCHS ENDOTHELIAL, 1 MIM:120252 COLLAGEN, TYPE VIII, ALPHA-2 COL8A2 HP:0001131 Corneal dystrophy FMA:58238 PATO:0001780 dystrophic ITM Feb 17, 2009
+MIM:136800 CORNEAL DYSTROPHY, FUCHS ENDOTHELIAL, 1 MIM:120252 COLLAGEN, TYPE VIII, ALPHA-2 COL8A2 HP:0003593 Early onset ITM Feb 17, 2009
+MIM:136800 CORNEAL DYSTROPHY, FUCHS ENDOTHELIAL, 1 MIM:120252 COLLAGEN, TYPE VIII, ALPHA-2 COL8A2 HP:0007705 Corneal degeneration TAS OMIM:136800 Feb 10, 2011
Added: phenotype-commons/annotations/OMIM/by-disease/annotated/MIM-211410.tab
===================================================================
--- phenotype-commons/annotations/OMIM/by-disease/annotated/MIM-211410.tab (rev 0)
+++ phenotype-commons/annotations/OMIM/by-disease/annotated/MIM-211410.tab 2011-12-31 11:41:42 UTC (rev 4117)
@@ -0,0 +1,3 @@
+Disease ID Disease Name Gene ID Gene Name Genotype Gene Symbol(s) Phenotype ID Phenotype Name Entity ID Entity Name Quality ID Quality Name Add'l Entity ID Add'l Entity Name Age of Onset ID Age of Onset Name Evidence Frequency Abnormal ID Abnormal Name Sex Negation ID Negation Name Description Orthologs Pub Date Created
+MIM:211410 BREAST CANCER, DUCTAL, 1 HP:0000007 Autosomal recessive inheritance IEA Feb 17, 2009
+MIM:211410 BREAST CANCER, DUCTAL, 1 HP:0006625 Breast cancer, frequently bilateral and multifocal IEA Feb 17, 2009
Added: phenotype-commons/annotations/OMIM/by-disease/annotated/MIM-211420.tab
===================================================================
--- phenotype-commons/annotations/OMIM/by-disease/annotated/MIM-211420.tab (rev 0)
+++ phenotype-commons/annotations/OMIM/by-disease/annotated/MIM-211420.tab 2011-12-31 11:41:42 UTC (rev 4117)
@@ -0,0 +1,3 @@
+Disease ID Disease Name Gene ID Gene Name Genotype Gene Symbol(s) Phenotype ID Phenotype Name Entity ID Entity Name Quality ID Quality Name Add'l Entity ID Add'l Entity Name Age of Onset ID Age of Onset Name Evidence Frequency Abnormal ID Abnormal Name Sex Negation ID Negation Name Description Orthologs Pub Date Created
+MIM:211420 BREAST CANCER, DUCTAL, 2 HP:0000007 Autosomal recessive inheritance IEA Feb 17, 2009
+MIM:211420 BREAST CANCER, DUCTAL, 2 HP:0006625 Breast cancer, frequently bilateral and multifocal IEA Feb 17, 2009
Added: phenotype-commons/annotations/OMIM/by-disease/annotated/MIM-278800.tab
===================================================================
--- phenotype-commons/annotations/OMIM/by-disease/annotated/MIM-278800.tab (rev 0)
+++ phenotype-commons/annotations/OMIM/by-disease/annotated/MIM-278800.tab 2011-12-31 11:41:42 UTC (rev 4117)
@@ -0,0 +1,27 @@
+Disease ID Disease Name Gene ID Gene Name Genotype Gene Symbol(s) Phenotype ID Phenotype Name Entity ID Entity Name Quality ID Quality Name Add'l Entity ID Add 'l Entity Name Mode of inheritance ID Mode of inheritance Name Age of Onset ID Age of Onset Name Evidence Frequency Abnormal ID Abnormal Name Description Orthologs Pub Date Created
+MIM:278800 DE SANCTIS-CACCHIONE SYNDROME MIM:609413 ERCC6 HP:0000007 IEA 17.02.2009
+MIM:278800 DE SANCTIS-CACCHIONE SYNDROME MIM:609413 ERCC6 HP:0000252 FMA:46565 PATO:0000587 IEA 17.02.2009
+MIM:278800 DE SANCTIS-CACCHIONE SYNDROME MIM:609413 ERCC6 HP:0000374 FMA:65132 HP:0000404 IEA 17.02.2009
+MIM:278800 DE SANCTIS-CACCHIONE SYNDROME MIM:609413 ERCC6 HP:0000491 IEA 17.02.2009
+MIM:278800 DE SANCTIS-CACCHIONE SYNDROME MIM:609413 ERCC6 HP:0000509 IEA 17.02.2009
+MIM:278800 DE SANCTIS-CACCHIONE SYNDROME MIM:609413 ERCC6 HP:0000613 IEA 17.02.2009
+MIM:278800 DE SANCTIS-CACCHIONE SYNDROME MIM:609413 ERCC6 HP:0000621 IEA 17.02.2009
+MIM:278800 DE SANCTIS-CACCHIONE SYNDROME MIM:609413 ERCC6 HP:0000656 FMA:54437 PATO:0001597 IEA 17.02.2009
+MIM:278800 DE SANCTIS-CACCHIONE SYNDROME MIM:609413 ERCC6 HP:0000992 FMA:54448 PATO:0000927 IEA 17.02.2009
+MIM:278800 DE SANCTIS-CACCHIONE SYNDROME MIM:609413 ERCC6 HP:0001009 IEA 17.02.2009
+MIM:278800 DE SANCTIS-CACCHIONE SYNDROME MIM:609413 ERCC6 HP:0001029 IEA 17.02.2009
+MIM:278800 DE SANCTIS-CACCHIONE SYNDROME MIM:609413 ERCC6 HP:0001251 GO:0050881 PATO:0000770 IEA 17.02.2009
+MIM:278800 DE SANCTIS-CACCHIONE SYNDROME MIM:609413 ERCC6 HP:0001257 IEA 17.02.2009
+MIM:278800 DE SANCTIS-CACCHIONE SYNDROME MIM:609413 ERCC6 HP:0001265 IEA 17.02.2009
+MIM:278800 DE SANCTIS-CACCHIONE SYNDROME MIM:609413 ERCC6 HP:0001266 IEA 17.02.2009
+MIM:278800 DE SANCTIS-CACCHIONE SYNDROME MIM:609413 ERCC6 HP:0001268 IEA 17.02.2009
+MIM:278800 DE SANCTIS-CACCHIONE SYNDROME MIM:609413 ERCC6 HP:0001284 IEA 17.02.2009
+MIM:278800 DE SANCTIS-CACCHIONE SYNDROME MIM:609413 ERCC6 HP:0001286 IEA 17.02.2009
+MIM:278800 DE SANCTIS-CACCHIONE SYNDROME MIM:609413 ERCC6 HP:0001480 ITM 17.02.2009
+MIM:278800 DE SANCTIS-CACCHIONE SYNDROME MIM:609413 ERCC6 HP:0001516 IEA 17.02.2009
+MIM:278800 DE SANCTIS-CACCHIONE SYNDROME MIM:609413 ERCC6 HP:0003079 IEA 17.02.2009
+MIM:278800 DE SANCTIS-CACCHIONE SYNDROME MIM:609413 ERCC6 HP:0003593 ITM 17.02.2009
+MIM:278800 DE SANCTIS-CACCHIONE SYNDROME MIM:609413 ERCC6 HP:0004334 FMA:7163 PATO:0001623 IEA 17.02.2009
+MIM:278800 DE SANCTIS-CACCHIONE SYNDROME MIM:609413 ERCC6 HP:0002542 IEA 28.12.2011
+MIM:278800 DE SANCTIS-CACCHIONE SYNDROME MIM:609413 ERCC6 HP:0001272 IEA 28.12.2011
+MIM:278800 DE SANCTIS-CACCHIONE SYNDROME MIM:609413 ERCC6 HP:0008639 FMA:18250 PATO:0000645 IEA 17.02.2009
Added: phenotype-commons/annotations/OMIM/by-disease/annotated/MIM-606966.tab
===================================================================
--- phenotype-commons/annotations/OMIM/by-disease/annotated/MIM-606966.tab (rev 0)
+++ phenotype-commons/annotations/OMIM/by-disease/annotated/MIM-606966.tab 2011-12-31 11:41:42 UTC (rev 4117)
@@ -0,0 +1,11 @@
+Disease ID Disease Name Gene ID Gene Name Genotype Gene Symbol(s) Phenotype ID Phenotype Name Entity ID Entity Name Quality ID Quality Name Add'l Entity ID Add 'l Entity Name Mode of inheritance ID Mode of inheritance Name Age of Onset ID Age of Onset Name Evidence Frequency Abnormal ID Abnormal Name Description Orthologs Pub Date Created
+MIM:606966 NEPHRONOPHTHISIS 4 MIM:607215 NPHP4 HP:0000007 IEA 17.02.2009
+MIM:606966 NEPHRONOPHTHISIS 4 MIM:607215 NPHP4 HP:0000090 IEA 17.02.2009
+MIM:606966 NEPHRONOPHTHISIS 4 MIM:607215 NPHP4 HP:0000103 GO:0060073 PATO:0000912 IEA 17.02.2009
+MIM:606966 NEPHRONOPHTHISIS 4 MIM:607215 NPHP4 HP:0000129 IEA 17.02.2009
+MIM:606966 NEPHRONOPHTHISIS 4 MIM:607215 NPHP4 HP:0001510 GO:0040007 PATO:0000911 IEA 17.02.2009
+MIM:606966 NEPHRONOPHTHISIS 4 MIM:607215 NPHP4 HP:0001903 IEA 17.02.2009
+MIM:606966 NEPHRONOPHTHISIS 4 MIM:607215 NPHP4 HP:0001959 GO:0042756 PATO:0000912 IEA 17.02.2009
+MIM:606966 NEPHRONOPHTHISIS 4 MIM:607215 NPHP4 HP:0003774 IEA 17.02.2009
+MIM:606966 NEPHRONOPHTHISIS 4 MIM:607215 NPHP4 HP:0000108 IEA 31.12.2011
+MIM:606966 NEPHRONOPHTHISIS 4 MIM:607215 NPHP4 HP:0000092 IEA 31.12.2011
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