NDDVD: an integrated and manually curated Neurodegenerative Diseases Variation Database.

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NDDVD: an integrated and manually curated Neurodegenerative Diseases Variation Database.

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http://www.wikidata.org/entity/Q55001686

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2018 nî lūn-bûn

@nan

2018年の論文

@ja

2018年学术文章

@wuu

2018年学术文章

@zh-cn

2018年学术文章

@zh-hans

2018年学术文章

@zh-my

2018年学术文章

@zh-sg

2018年學術文章

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2018年學術文章

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2018年學術文章

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name

NDDVD: an integrated and manually curated Neurodegenerative Diseases Variation Database.

@en

NDDVD: an integrated and manually curated Neurodegenerative Diseases Variation Database.

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type

Item

label

NDDVD: an integrated and manually curated Neurodegenerative Diseases Variation Database.

@en

NDDVD: an integrated and manually curated Neurodegenerative Diseases Variation Database.

@nl

prefLabel

NDDVD: an integrated and manually curated Neurodegenerative Diseases Variation Database.

@en

NDDVD: an integrated and manually curated Neurodegenerative Diseases Variation Database.

@nl

P1476

NDDVD: an integrated and manually curated Neurodegenerative Diseases Variation Database.

@en

P2093

Bairong Shen

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

Chao Xu

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

Chen Xu

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

Li Shen

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

Mauno Vihinen

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

Xingyun Liu

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

Yang Yang

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

Yuanyuan Zhang

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P2860

Pathogenic mechanisms of a polyglutamine-mediated neurodegenerative disease, spinocerebellar ataxia type 1

The amino-acid mutational spectrum of human genetic disease

PON-P2: prediction method for fast and reliable identification of harmful variants

Variation Ontology for annotation of variation effects and mechanisms

Predicting the effects of coding non-synonymous variants on protein function using the SIFT algorithm

Mutation nomenclature extensions and suggestions to describe complex mutations: a discussion

Conservation and covariance in PH domain sequences: physicochemical profile and information theoretical analysis of XLA-causing mutations in the Btk PH domain.

Physicochemical feature-based classification of amino acid mutations.

Pathogenic or not? And if so, then how? Studying the effects of missense mutations using bioinformatics methods.

A mutation database for amyotrophic lateral sclerosis.

P31

scholarly article

P356

10.1093/DATABASE/BAY018

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P478

2018

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P577

2018-01-01T00:00:00Z

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P698

29688368

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P921

neurodegeneration

Base de dados

P932

5841369

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