MouseFinder: Candidate disease genes from mouse phenotype data. - Wikidata - awgldk - TriplyDB

MouseFinder: Candidate disease genes from mouse phenotype data.

MouseFinder: Candidate disease genes from mouse phenotype data.

http://www.wikidata.org/entity/Q34158189

about

Robust and sensitive analysis of mouse knockout phenotypes Unification of multi-species vertebrate anatomy ontologies for comparative biology in Uberon Mouse genetic and phenotypic resources for human genetics Disease insights through cross-species phenotype comparisons The Human Phenotype Ontology project: linking molecular biology and disease through phenotype data The Human Phenotype Ontology in 2017 Toward knowledge support for analysis and interpretation of complex traits The Mammalian Phenotype Ontology as a unifying standard for experimental and high-throughput phenotyping data Improving disease gene prioritization by comparing the semantic similarity of phenotypes in mice with those of human diseases.The ontology of craniofacial development and malformation for translational craniofacial research PhenomeCentral: a portal for phenotypic and genotypic matchmaking of patients with rare genetic diseases The influence of disease categories on gene candidate predictions from model organism phenotypes.Finding our way through phenotypes.Automatic concept recognition using the human phenotype ontology reference and test suite corpora.PhenoDigm: analyzing curated annotations to associate animal models with human diseases.A knowledge based approach to matching human neurodegenerative disease and animal models The mouse pathology ontology, MPATH; structure and applications.Mouse model phenotypes provide information about human drug targets.Linking tissues to phenotypes using gene expression profiles Deep phenotyping for precision medicine.The facial evolution: looking backward and moving forward.Analysis of the human diseasome using phenotype similarity between common, genetic, and infectious diseases Capturing domain knowledge from multiple sources: the rare bone disorders use case.Similarity-based search of model organism, disease and drug effect phenotypes Integration of global resources for human genetic variation and disease.The zebrafish anatomy and stage ontologies: representing the anatomy and development of Danio rerio.Construction and accessibility of a cross-species phenotype ontology along with gene annotations for biomedical research.Automatically transforming pre- to post-composed phenotypes: EQ-lising HPO and MP.Autosomal recessive spinocerebellar ataxia 7 (SCAR7) is caused by variants in TPP1, the gene involved in classic late-infantile neuronal ceroid lipofuscinosis 2 disease (CLN2 disease).PhenoRank: reducing study bias in gene prioritisation through simulation.Use of animal models for exome prioritization of rare disease genes Mouse Genetic and Phenotypic Resources as Tools for Human Genetics Semantic Disease Gene Embeddings (SmuDGE): phenotype-based disease gene prioritization without phenotypes

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P2860

MouseFinder: Candidate disease genes from mouse phenotype data.

http://www.wikidata.org/entity/Q34158189

description

2012 nî lūn-bûn

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2012 թուականի Մարտին հրատարակուած գիտական յօդուած

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2012 թվականի մարտին հրատարակված գիտական հոդված

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2012年の論文

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2012年論文

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2012年論文

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2012年論文

@zh-hk

2012年論文

@zh-mo

2012年論文

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2012年论文

@wuu

name

MouseFinder: Candidate disease genes from mouse phenotype data.

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MouseFinder: Candidate disease genes from mouse phenotype data.

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MouseFinder: Candidate disease genes from mouse phenotype data.

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type

label

MouseFinder: Candidate disease genes from mouse phenotype data.

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MouseFinder: Candidate disease genes from mouse phenotype data.

@en

MouseFinder: Candidate disease genes from mouse phenotype data.

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prefLabel

MouseFinder: Candidate disease genes from mouse phenotype data.

@ast

MouseFinder: Candidate disease genes from mouse phenotype data.

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MouseFinder: Candidate disease genes from mouse phenotype data.

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MouseFinder: Candidate disease genes from mouse phenotype data.

@en

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Chao-Kung Chen

http://www.w3.org/2001/XMLSchema#string

Monte Westerfield

http://www.w3.org/2001/XMLSchema#string

Paul N Schofield

http://www.w3.org/2001/XMLSchema#string

Sandra C Doelken

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Suzanna E Lewis

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P2860

Linking human diseases to animal models using ontology-based phenotype annotation

A conditional knockout resource for the genome-wide study of mouse gene function

Integrating phenotype ontologies across multiple species

The IKMC web portal: a central point of entry to data and resources from the International Knockout Mouse Consortium

The Mouse Genome Database (MGD): premier model organism resource for mammalian genomics and genetics

PhenomicDB: a new cross-species genotype/phenotype resource

The mouse ascending: perspectives for human-disease models

Artemin is a vascular-derived neurotropic factor for developing sympathetic neurons

Laboratory mouse models for the human genome-wide associations

FlyBase: enhancing Drosophila Gene Ontology annotations

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858-866

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10.1002/HUMU.22051

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5

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33

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Barbara J. Ruef

Sebastian Köhler

Georgios V. Gkoutos

Cynthia L Smith

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2012-03-16T00:00:00Z

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221830015

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22331800

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3327758

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