Mapping genotype-phenotype associations of nsSNPs in coiled-coil oligomerization domains of the human proteome.

about

Mapping genotype-phenotype associations of nsSNPs in coiled-coil oligomerization domains of the human proteome.

Item

http://www.wikidata.org/entity/Q48164751

description

2017 nî lūn-bûn

@nan

2017年の論文

@ja

2017年学术文章

@wuu

2017年学术文章

@zh-cn

2017年学术文章

@zh-hans

2017年学术文章

@zh-my

2017年学术文章

@zh-sg

2017年學術文章

@yue

2017年學術文章

@zh

2017年學術文章

@zh-hant

name

Mapping genotype-phenotype ass ...... domains of the human proteome.

@en

Mapping genotype-phenotype ass ...... domains of the human proteome.

@nl

type

Item

label

Mapping genotype-phenotype ass ...... domains of the human proteome.

@en

Mapping genotype-phenotype ass ...... domains of the human proteome.

@nl

prefLabel

Mapping genotype-phenotype ass ...... domains of the human proteome.

@en

Mapping genotype-phenotype ass ...... domains of the human proteome.

@nl

P1476

Mapping genotype-phenotype ass ...... domains of the human proteome.

@en

P2093

Andrzej Goscinski

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

Kaavya A Mohanasundaram

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

Mani P Grover

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

Tamsyn M Crowley

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

P2860

Finding the missing heritability of complex diseases

Conserved segments 1A and 2B of the intermediate filament dimer: their atomic structures and role in filament assembly

The coiled-coil domain containing protein CCDC40 is essential for motile cilia function and left-right axis formation

Online Mendelian Inheritance in Man (OMIM), a knowledgebase of human genes and genetic disorders

The NHGRI GWAS Catalog, a curated resource of SNP-trait associations

Sequence variation in G-protein-coupled receptors: analysis of single nucleotide polymorphisms

Disease mutations in disordered regions--exception to the rule?

X-ray structure of the GCN4 leucine zipper, a two-stranded, parallel coiled coil

A novel keratin 5 mutation (K5V186L) in a family with EBS-K: a conservative substitution can lead to development of different disease phenotypes

Conformational parameters for amino acids in helical, beta-sheet, and random coil regions calculated from proteins

P304

1378-1393

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

P31

scholarly article

P356

10.1002/HUMU.23252

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

P433

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

P478

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

P50

Merridee A. Wouters

P577

2017-05-10T00:00:00Z

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

P698

28489284

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