(Q24570119)

6

0 references

Doron Lancet

11

0 references

Noam Nativ

2

0 references

Iris Bahir

7

0 references

Gil Stelzer

3

0 references

Frida Belinky

8

0 references

author name string

Noa Rappaport

1

0 references

Michal Twik

4

0 references

Yaron Guan-Golan

5

0 references

C Paul Morrey

Creative Commons Attribution-NonCommercial 3.0 Unported

9

0 references

language of work or name

English

0 references

publication date

2013

0 references

published in

Database

0 references

volume

2013

0 references

issue

0

0 references

page(s)

bat018

0 references

copyright license

start time

3 October 2016

1 reference

April 2022 Public Data File from Crossref

copyright status

copyrighted

0 references

cites work

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1 reference

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Gene-disease network analysis reveals functional modules in mendelian, complex and environmental diseases

24 March 2017

1 reference

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GeneCards Version 3: the human gene integrator

24 March 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3625956

Network organization of the human autophagy system

24 March 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3625956

The implications of human metabolic network topology for disease comorbidity

24 March 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3625956

The human disease network

24 March 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3625956

Network medicine: a network-based approach to human disease

24 March 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3625956

Genome-wide association studies for common diseases and complex traits

7 April 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3625956

Effective mapping of biomedical text to the UMLS Metathesaurus: the MetaMap program

7 April 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3625956

GenomeRNAi: a database for cell-based and in vivo RNAi phenotypes, 2013 update.

7 April 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3625956

Mutation in TECPR2 reveals a role for autophagy in hereditary spastic paraparesis

27 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3625956

Non-redundant compendium of human ncRNA genes in GeneCards

27 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3625956

The Comparative Toxicogenomics Database: update 2013.

27 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3625956

MEDIC: a practical disease vocabulary used at the Comparative Toxicogenomics Database.

27 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3625956

Disease Ontology: a backbone for disease semantic integration

27 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3625956

A new face and new challenges for Online Mendelian Inheritance in Man (OMIM®).

27 September 2017

1 reference

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Toward an ontological treatment of disease and diagnosis

27 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3625956

An overview of MetaMap: historical perspective and recent advances

27 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3625956

GeneDecks: paralog hunting and gene-set distillation with GeneCards annotation

27 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3625956

A network medicine approach to human disease

27 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3625956

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

27 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3625956

An analysis of human microRNA and disease associations

27 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3625956

Probing genetic overlap among complex human phenotypes.

27 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3625956

Sudden-onset blindness in sickle cell disease due to retinal artery occlusion

27 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3625956

GeneTests: an online genetic information resource for health care providers.

27 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3625956

The HUGO Gene Nomenclature Committee (HGNC).

27 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3625956

Evaluation of the content coverage of SNOMED CT: ability of SNOMED clinical terms to represent clinical problem lists.

27 September 2017

1 reference

Crossref

https://api.crossref.org/works/10.1093%2FDATABASE%2FBAT018

The impact of cellular networks on disease comorbidity

21 January 2018

1 reference

Crossref

https://api.crossref.org/works/10.1093%2FDATABASE%2FBAT018

The Unified Medical Language System

21 January 2018

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/23584832

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

Searching Online Mendelian Inheritance in Man (OMIM) for information on genetic loci involved in human disease

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/23584832

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

Short stature in children with sickle cell anemia correlates with alterations in the IGF-I axis

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/23584832

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

Identifiers

DOI

10.1093/DATABASE/BAT018

1 reference

535438

535438

1 reference

1 reference

1 reference