URL: https://www.hmtphenome.uniba.it
Proper Citation: HmtPhenome (RRID:SCR_017289)
Description: Collection of data about variants, genes, phenotypes and diseases involved in mitochondrial functionality. Users can search for variant position, gene, phenotype or disease and retrieve all related information through integrated network of biological entities.
Resource Type: software resource, data or information resource, software application, service resource, database, data processing software, network graph visualization software, data visualization software
Defining Citation: DOI:10.1101/660282
Keywords: mitochondria, variant, gene, function, phenotype, data
Expand Alluses |
|
uses |
|
uses |
|
uses |
|
uses |
|
has parent organization |
We found {{ ctrl2.mentions.total_count }} mentions in open access literature.
We have not found any literature mentions for this resource.
We are searching literature mentions for this resource.
Most recent articles:
{{ mention._source.dc.creators[0].familyName }} {{ mention._source.dc.creators[0].initials }}, et al. ({{ mention._source.dc.publicationYear }}) {{ mention._source.dc.title }} {{ mention._source.dc.publishers[0].name }}, {{ mention._source.dc.publishers[0].volume }}({{ mention._source.dc.publishers[0].issue }}), {{ mention._source.dc.publishers[0].pagination }}. (PMID:{{ mention._id.replace('PMID:', '') }})
Check
for all resource mentions.
A list of researchers who have used the resource and an author search tool
Find mentions based on location
{{ ctrl2.mentions.errors.location }}
A list of researchers who have used the resource and an author search tool. This is available for resources that have literature mentions.
No rating or validation information has been found for HmtPhenome.
No alerts have been found for HmtPhenome.
Source: SciCrunch Registry
