(Q33503917)

27 July 2017

Between proteins and phenotypes: annotation and interpretation of mutations (English)

1 reference

Dietrich Rebholz-Schuhmann

27 July 2017

series ordinal

2

object named as

Dietrich Rebholz-Schuhmann

1 reference

27 July 2017

Christopher J O Baker

series ordinal

1

1 reference

PubMed ID

19758463

27 July 2017

language of work or name

English

0 references

publication date

27 August 2009

1 reference

27 July 2017

1 reference

27 July 2017

10 Suppl 8

1 reference

27 July 2017

I1

1 reference

Creative Commons Attribution 2.0 Generic

27 July 2017

S8

0 references

copyright license

start time

1 August 2009

1 reference

April 2022 Public Data File from Crossref

copyright status

copyrighted

0 references

exact match

https://scigraph.springernature.com/pub.10.1186/1471-2105-10-s8-i1

0 references

cites work

Using structural bioinformatics to investigate the impact of non synonymous SNPs and disease mutations: scope and limitations

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2745581

Correlating protein function and stability through the analysis of single amino acid substitutions.

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2745581

MtSNPscore: a combined evidence approach for assessing cumulative impact of mitochondrial variations in disease

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2745581

From SNPs to pathways: integration of functional effect of sequence variations on models of cell signalling pathways

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2745581

An integrated approach to the interpretation of single amino acid polymorphisms within the framework of CATH and Gene3D.

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2745581

Annotation of protein residues based on a literature analysis: cross-validation against UniProtKb

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2745581

Improved mutation tagging with gene identifiers applied to membrane protein stability prediction

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2745581

EnzyMiner: automatic identification of protein level mutations and their impact on target enzymes from PubMed abstracts

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2745581

Pairwise and higher-order correlations among drug-resistance mutations in HIV-1 subtype B protease

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2745581

Extraction of human kinase mutations from literature, databases and genotyping studies

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2745581

PhenoGO: an integrated resource for the multiscale mining of clinical and biological data

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2745581

The Human Phenotype Ontology: a tool for annotating and analyzing human hereditary disease

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2745581

A workflow for mutation extraction and structure annotation.

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2745581

The OBO Foundry: coordinated evolution of ontologies to support biomedical data integration

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2745581

SNAP: predict effect of non-synonymous polymorphisms on function

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2745581

The genetic association database

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2745581

Automatic extraction of mutations from Medline and cross-validation with OMIM.

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2745581

Making sense of mutation requires knowledge management

21 June 2018

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/19758463

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

Identifiers

DOI

10.1186/1471-2105-10-S8-I1

1 reference

PubMed ID

19758463

Dimensions Publication ID

27 July 2017

0 references

1 reference

27 July 2017

1 reference

PubMed ID

19758463