CHDGKB
CHDGKB (A knowledgebase of non-syndromic congenital heart disease genetic variations) is a manually curated database of genetic variations associated with non syndromic congenital heart disease. CHDGKB contains a comprehensive information of genetic variations for 370 subtypes of human congenital heart disease reported in PubMed from 1998, which would provide an exhaustive and summary of current status of non-syndromic CHD genetic research that can contribute to better interpret the human variants for illustrating NS-CHD causing variants.
Description
More detailed information about this field from each metasource.
CHDGKB (A knowledgebase of non-syndromic congenital heart disease genetic variations) is a manually curated database of genetic variations associated with non syndromic congenital heart disease. CHDGKB contains a comprehensive information of genetic variations for 370 subtypes of human congenital heart disease reported in PubMed from 1998, which would provide an exhaustive and summary of current status of non-syndromic CHD genetic research that can contribute to better interpret the human variants for illustrating NS-CHD causing variants.
metasource: bio.toolsversion: extracted_at: 2022-11-04T11:28:34.404865
Webpage:
http://www.sysbio.org.cn/CHDGKB/Webpage
More detailed information about this field from each metasource.
http://www.sysbio.org.cn/CHDGKB/
metasource: bio.toolsversion: extracted_at: 2022-11-04T11:28:34.404865
Publications:
Publications
More detailed information about this field from each metasource.
CHDGKB: a knowledgebase for systematic understanding of genetic variations associated with non-syndromic congenital heart disease
PMID: 32608479
metasource: bio.tools
version: extracted_at: 2022-11-04T11:28:34.404865
Publications
More detailed information about this field from each metasource.
CHDGKB: a knowledgebase for systematic understanding of genetic variations associated with non-syndromic congenital heart disease
PMID: 32608479
metasource: bio.tools
version: extracted_at: 2022-11-04T11:28:34.404865
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CHDGKB: a knowledgebase for systematic understanding of genetic variations associated with non-syndromic congenital heart disease
PubMed citations: 2.
2 articles citing: CHDGKB: a knowledgebase for systematic understanding of genetic variations associated with non-syndromic congenital heart disease
MIKB: A manually curated and comprehensive knowledge base for myocardial infarction. PMID:34900127
An update on the CHDGKB for the systematic understanding of risk factors associated with non-syndromic congenital heart disease. PMID:34765091
Tags:
Tags
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cardiology
metasource: bio.tools
version: extracted_at: 2022-11-04T11:28:34.404865
genetic variation
metasource: bio.tools
version: extracted_at: 2022-11-04T11:28:34.404865
genotype and phenotype
metasource: bio.tools
version: extracted_at: 2022-11-04T11:28:34.404865
pathology
metasource: bio.tools
version: extracted_at: 2022-11-04T11:28:34.404865
gene expression
metasource: bio.tools
version: extracted_at: 2022-11-04T11:28:34.404865
Tags
More detailed information about this field from each metasource.
cardiology
metasource: bio.toolsversion: extracted_at: 2022-11-04T11:28:34.404865
genetic variation
metasource: bio.toolsversion: extracted_at: 2022-11-04T11:28:34.404865
genotype and phenotype
metasource: bio.toolsversion: extracted_at: 2022-11-04T11:28:34.404865
pathology
metasource: bio.toolsversion: extracted_at: 2022-11-04T11:28:34.404865
gene expression
metasource: bio.toolsversion: extracted_at: 2022-11-04T11:28:34.404865
cardiology genetic variation genotype and phenotype pathology gene expression
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