(Q28584435)

3

0 references

Laura I. Furlong

9

0 references

Janet Piñero

1

0 references

Ferran Sanz

object named as

Ferran Sanz

8

0 references

author name string

Àlex Bravo

2

0 references

Alba Gutiérrez-Sacristán

4

0 references

Jordi Deu-Pons

5

0 references

Emilio Centeno

6

0 references

Javier García-García

Creative Commons Attribution-NonCommercial 4.0 International

7

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language of work or name

English

0 references

publication date

4 January 2017

0 references

published in

Nucleic Acids Research

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volume

45

0 references

page(s)

D833-D839

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issue

D1

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copyright license

start time

4 January 2017

1 reference

April 2022 Public Data File from Crossref

copyright status

copyrighted

0 references

cites work

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17 March 2017

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17 March 2017

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17 March 2017

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Network medicine analysis of COPD multimorbidities

17 March 2017

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17 March 2017

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The EBI RDF platform: linked open data for the life sciences

17 March 2017

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A computational framework to infer human disease-associated long noncoding RNAs

17 March 2017

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17 March 2017

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Extraction of semantic biomedical relations from text using conditional random fields

17 March 2017

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17 March 2017

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UniProt: a hub for protein information

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The Unified Medical Language System (UMLS): integrating biomedical terminology

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Association Study for 26 Candidate Loci in Idiopathic Pulmonary Fibrosis Patients from Four European Populations

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Causal Mechanistic Regulatory Network for Glioblastoma Deciphered Using Systems Genetics Network Analysis.

29 September 2017

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Candidate gene networks and blood biomarkers of methamphetamine-associated psychosis: an integrative RNA-sequencing report

29 September 2017

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Uncovering disease mechanisms through network biology in the era of Next Generation Sequencing

29 September 2017

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Characterization of clinical signs in the human interactome

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29 September 2017

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29 September 2017

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29 September 2017

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Exploring the cellular basis of human disease through a large-scale mapping of deleterious genes to cell types

29 September 2017

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Molecular and clinical diseasome of comorbidities in exacerbated COPD patients

29 September 2017

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Novel scripts for improved annotation and selection of variants from whole exome sequencing in cancer research

29 September 2017

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The support of human genetic evidence for approved drug indications

29 September 2017

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Genetic mutations associated with status epilepticus.

29 September 2017

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TFmiR: a web server for constructing and analyzing disease-specific transcription factor and miRNA co-regulatory networks

29 September 2017

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OMIM.org: Online Mendelian Inheritance in Man (OMIM®), an online catalog of human genes and genetic disorders

29 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5210640

The Rat Genome Database 2015: genomic, phenotypic and environmental variations and disease

29 September 2017

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The Mouse Genome Database (MGD): facilitating mouse as a model for human biology and disease

29 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5210640

The Comparative Toxicogenomics Database's 10th year anniversary: update 2015.

29 September 2017

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Organ system heterogeneity DB: a database for the visualization of phenotypes at the organ system level

29 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5210640

Systematic analysis of gene properties influencing organ system phenotypes in mammalian perturbations

29 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5210640

A knowledge-driven approach to extract disease-related biomarkers from the literature

29 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5210640

Prioritizing disease-linked variants, genes, and pathways with an interactive whole-genome analysis pipeline

29 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5210640

Representation of rare diseases in health information systems: the Orphanet approach to serve a wide range of end users

29 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5210640

DisGeNET: a Cytoscape plugin to visualize, integrate, search and analyze gene-disease networks

29 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5210640

Publishing DisGeNET as nanopublications

29 September 2017

1 reference

Crossref

https://api.crossref.org/works/10.1093%2FNAR%2FGKW943

ncPred: ncRNA-Disease Association Prediction through Tripartite Network-Based Inference.

21 January 2018

1 reference

Crossref

https://api.crossref.org/works/10.1093%2FNAR%2FGKW943

journals/nar/PineroBQGDCGSF17

21 January 2018

Identifiers

DOI

10.1093/NAR/GKW943

0 references

DBLP publication ID

1 reference