Mercurial > hgweb > health
changeset 5317:7154827f915f
task #16230: Use grouped attribute for large datafiles. Implement it on Genetics and Uniprot
| author | Luis Falcon <falcon@gnuhealth.org> |
|---|---|
| date | Wed, 14 Sep 2022 10:17:12 +0100 |
| parents | 1c9d314c2820 |
| children | e70ca5cae10a |
| files | tryton/health_genetics/data/disease_genes.xml tryton/health_genetics_uniprot/data/gene_variants.xml tryton/health_genetics_uniprot/data/protein_diseases.xml tryton/health_genetics_uniprot/data/variant_phenotypes.xml |
| diffstat | 4 files changed, 4 insertions(+), 4 deletions(-) [+] |
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--- a/tryton/health_genetics/data/disease_genes.xml +++ b/tryton/health_genetics/data/disease_genes.xml @@ -1,6 +1,6 @@ <?xml version="1.0" encoding="utf-8" ?> <tryton> -<data noupdate="0" skiptest="1"> +<data skiptest="1" noupdate="1" grouped="1"> <record model="gnuhealth.disease.gene" id="A2BP1"> <field name="name">A2BP1</field> <field name="long_name">ataxin 2-binding protein 1</field>
--- a/tryton/health_genetics_uniprot/data/gene_variants.xml +++ b/tryton/health_genetics_uniprot/data/gene_variants.xml @@ -1,6 +1,6 @@ <?xml version="1.0" encoding="utf-8" ?> <tryton> -<data noupdate="0"> +<data skiptest="1" noupdate="1" grouped="1"> <record model="gnuhealth.gene.variant" id="VAR_012804"> <field name="name" ref="health_genetics.AAAS"></field> <field name="variant">VAR_012804</field>
--- a/tryton/health_genetics_uniprot/data/protein_diseases.xml +++ b/tryton/health_genetics_uniprot/data/protein_diseases.xml @@ -1,6 +1,6 @@ <?xml version="1.0" encoding="utf-8" ?> <tryton> -<data noupdate="0"> +<data skiptest="1" noupdate="1" grouped="1"> <record model="gnuhealth.protein.disease" id="DI-00001"> <field name="name">DI-00001</field> <field name="disease_name">HDS10 mitochondrial disease</field>
--- a/tryton/health_genetics_uniprot/data/variant_phenotypes.xml +++ b/tryton/health_genetics_uniprot/data/variant_phenotypes.xml @@ -1,6 +1,6 @@ <?xml version="1.0" encoding="utf-8" ?> <tryton> -<data noupdate="0"> +<data skiptest="1" noupdate="1" grouped="1"> <record model="gnuhealth.gene.variant.phenotype" id="VARPHEN1"> <field name="name">VARPHEN1</field> <field name="variant" ref="VAR_001767"></field>
