(Q89941828)

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:32110491%20AND%20SRC:MED&resulttype=core&format=json

9 April 2020

title

DISNET: a framework for extracting phenotypic disease information from public sources (English)

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:32110491%20AND%20SRC:MED&resulttype=core&format=json

9 April 2020

author name string

Gerardo Lagunes-García

1

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:32110491%20AND%20SRC:MED&resulttype=core&format=json

9 April 2020

Alejandro Rodríguez-González

2

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:32110491%20AND%20SRC:MED&resulttype=core&format=json

9 April 2020

Lucía Prieto-Santamaría

3

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:32110491%20AND%20SRC:MED&resulttype=core&format=json

9 April 2020

Eduardo P García Del Valle

4

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:32110491%20AND%20SRC:MED&resulttype=core&format=json

9 April 2020

Massimiliano Zanin

5

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:32110491%20AND%20SRC:MED&resulttype=core&format=json

9 April 2020

Ernestina Menasalvas-Ruiz

6

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:32110491%20AND%20SRC:MED&resulttype=core&format=json

9 April 2020

publication date

17 February 2020

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:32110491%20AND%20SRC:MED&resulttype=core&format=json

9 April 2020

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:32110491%20AND%20SRC:MED&resulttype=core&format=json

9 April 2020

volume

8

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:32110491%20AND%20SRC:MED&resulttype=core&format=json

9 April 2020

page(s)

e8580

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:32110491%20AND%20SRC:MED&resulttype=core&format=json

Creative Commons Attribution 4.0 International

9 April 2020

copyright license

start time

17 February 2020

1 reference

April 2022 Public Data File from Crossref

copyright status

copyrighted

0 references

describes a project that uses

Cytoscape

object named as

Cytoscape

1 reference

CZ Software Mentions: A large dataset of software mentions in the biomedical literature

cites work

KEGG: kyoto encyclopedia of genes and genomes

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12 December 2020

Medical Subject Headings (MeSH).

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12 December 2020

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

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12 December 2020

GeneCards 2002: towards a complete, object-oriented, human gene compendium

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12 December 2020

Discovering genotypes underlying human phenotypes: past successes for mendelian disease, future approaches for complex disease

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12 December 2020

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

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12 December 2020

A text-mining analysis of the human phenome

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12 December 2020

The comparative toxicogenomics database: a cross-species resource for building chemical-gene interaction networks

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12 December 2020

The human disease network

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12 December 2020

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

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12 December 2020

A network medicine approach to human disease

1 reference

12 December 2020

An evaluation of medical knowledge contained in Wikipedia and its use in the LOINC database

1 reference

12 December 2020

Mayo clinical Text Analysis and Knowledge Extraction System (cTAKES): architecture, component evaluation and applications

1 reference

12 December 2020

Network medicine: a network-based approach to human disease

1 reference

12 December 2020

Prioritizing candidate disease genes by network-based boosting of genome-wide association data.

1 reference

12 December 2020

Disease Ontology: a backbone for disease semantic integration

1 reference

12 December 2020

MalaCards: an integrated compendium for diseases and their annotation

1 reference

12 December 2020

mentha: a resource for browsing integrated protein-interaction networks

1 reference

12 December 2020

An innovative portal for rare genetic diseases research: the semantic Diseasecard

1 reference

12 December 2020

The Human Gene Mutation Database: building a comprehensive mutation repository for clinical and molecular genetics, diagnostic testing and personalized genomic medicine

1 reference

12 December 2020

Activities at the Universal Protein Resource (UniProt)

1 reference

12 December 2020

Evaluation of gastroenterology and hepatology articles on Wikipedia: are they suitable as learning resources for medical students?

1 reference

12 December 2020

Wikipedia vs peer-reviewed medical literature for information about the 10 most costly medical conditions

1 reference

12 December 2020

Human symptoms-disease network

1 reference

12 December 2020

Network based integrated analysis of phenotype-genotype data for prioritization of candidate symptom genes

1 reference

12 December 2020

MalaCards: A Comprehensive Automatically-Mined Database of Human Diseases.

1 reference

12 December 2020

Comparative analysis of a novel disease phenotype network based on clinical manifestations

1 reference

12 December 2020

DISEASES: Text mining and data integration of disease–gene associations

1 reference

12 December 2020

Motivations for contributing to health-related articles on Wikipedia: an interview study

1 reference

12 December 2020

PhosphoSitePlus, 2014: mutations, PTMs and recalibrations

1 reference

12 December 2020

The readability of the English Wikipedia article on Parkinson's disease

1 reference

12 December 2020

Is Wikipedia a reliable learning resource for medical students? Evaluating respiratory topics.

1 reference

12 December 2020

Wikipedia and medicine: quantifying readership, editors, and the significance of natural language

1 reference

12 December 2020

Analysis of the human diseasome using phenotype similarity between common, genetic, and infectious diseases

1 reference

12 December 2020

SIGNOR: a database of causal relationships between biological entities.

1 reference

12 December 2020

DiMeX: A Text Mining System for Mutation-Disease Association Extraction.

1 reference

12 December 2020

Text mining for precision medicine: automating disease-mutation relationship extraction from biomedical literature

1 reference

12 December 2020

DTMiner: identification of potential disease targets through biomedical literature mining

1 reference

12 December 2020

Why Medical Schools Should Embrace Wikipedia: Final-Year Medical Student Contributions to Wikipedia Articles for Academic Credit at One School

1 reference

12 December 2020

The Human Phenotype Ontology in 2017

1 reference

12 December 2020

DisGeNET: a comprehensive platform integrating information on human disease-associated genes and variants

1 reference

12 December 2020

Evolution of Wikipedia's medical content: past, present and future

1 reference

12 December 2020

What can Google and Wikipedia can tell us about a disease? Big Data trends analysis in Systemic Lupus Erythematosus

1 reference

12 December 2020

DISNOR: a disease network open resource.

1 reference

12 December 2020

PedAM: a database for Pediatric Disease Annotation and Medicine

1 reference

12 December 2020

Text mining of rheumatoid arthritis and diabetes mellitus to understand the mechanisms of Chinese medicine in different diseases with same treatment.

1 reference

12 December 2020

A comprehensive and quantitative comparison of text-mining in 15 million full-text articles versus their corresponding abstracts.

1 reference

12 December 2020

DEXTER: Disease-Expression Relation Extraction from Text.

1 reference

12 December 2020

More than 2 billion pairs of eyeballs: Why aren't you sharing medical knowledge on Wikipedia?

1 reference

12 December 2020

Best Match: New relevance search for PubMed

1 reference

12 December 2020

HumanNet v2: human gene networks for disease research

1 reference

12 December 2020

STRING v11: protein–protein association networks with increased coverage, supporting functional discovery in genome-wide experimental datasets

1 reference

12 December 2020

Mining Disease-Symptom Relation from Massive Biomedical Literature and Its Application in Severe Disease Diagnosis

1 reference

12 December 2020

Disease networks and their contribution to disease understanding: A review of their evolution, techniques and data sources

1 reference

12 December 2020

Excavating the mother lode of human-generated text: A systematic review of research that uses the wikipedia corpus

0 references

Identifiers

DOI

10.7717/PEERJ.8580

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:32110491%20AND%20SRC:MED&resulttype=core&format=json

9 April 2020

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:32110491%20AND%20SRC:MED&resulttype=core&format=json

9 April 2020

PubMed publication ID

32110491

1 reference