Next generation phenotyping using narrative reports in a rare disease clinical data warehouse release_vgagwi6sabgnbcctpx2uz3rrka

by Nicolas Garcelon, Antoine Neuraz, Rémi Salomon, Nadia Bahi-Buisson, Jeanne Amiel, Capucine Picard, Nizar Mahlaoui, Vincent Benoit, Anita Burgun, Bastien Rance

Published in Orphanet Journal of Rare Diseases by Springer Nature.

2018   Volume 13

Archived Files and Locations

application/pdf  1.4 MB
file_dv5ihw67l5e4npmnxn5twoy4cm
web.archive.org (webarchive)
pdfs.semanticscholar.org (aggregator)
Read Archived PDF
Preserved and Accessible
Type  article-journal
Stage   published
Date   2018-05-31
Language   en ?
DOI  10.1186/s13023-018-0830-6
PubMed  29855327
PMC  PMC5984368
Wikidata  Q54977447
Journal Metadata
Open Access Publication
In DOAJ
In ISSN ROAD
In Keepers Registry
ISSN-L:  1750-1172
Work Entity
access all versions, variants, and formats of this works (eg, pre-prints)
Catalog Record
Revision: c7227897-a07f-471e-b832-9727925b7dcc
API URL: JSON