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Resource Name
HmtPhenome
RRID:SCR_017289 RRID Copied      
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HmtPhenome (RRID:SCR_017289)
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Resource Information

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: network graph visualization software, software application, data processing software, data visualization software, database, software resource, data or information resource, service resource

Defining Citation: DOI:10.1101/660282

Keywords: mitochondria, variant, gene, function, phenotype, data

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This resource

uses

Human Phenotype Ontology

uses

Ensembl

uses

OMIM

uses

Orphanet

uses

DisGeNET

has parent organization

University of Bari; Bari; Italy

Usage and Citation Metrics

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Data and Source Information