reference/22894434

http://rdf.ncbi.nlm.nih.gov/pubchem/reference/22894434

Outgoing Links

Predicate	Object
contentType	Journal Article
endingPage	760
issn	1468-6244 0022-2593
issueIdentifier	11
pageRange	752-760
publicationName	Journal of Medical Genetics
startingPage	752
bibliographicCitation	Lopez E, Berenguer M, Tingaud-Sequeira A, Marlin S, Toutain A, Denoyelle F, Picard A, Charron S, Mathieu G, de Belvalet H, Arveiler B, Babin PJ, Lacombe D, Rooryck C. Mutations in MYT1, encoding the myelin transcription factor 1, are a rare cause of OAVS. J Med Genet. 2016 Nov;53(11):752–60. doi: 10.1136/jmedgenet-2016-103774. PMID: 27358179.
creator	http://rdf.ncbi.nlm.nih.gov/pubchem/author/MD5_9e4bef449abdb2c9d229d374d416f14f http://rdf.ncbi.nlm.nih.gov/pubchem/author/MD5_92f21abb685aa89e9aa7c5c92917a07b http://rdf.ncbi.nlm.nih.gov/pubchem/author/MD5_caac96d0edb4ad5da1ebeaca5fee63a6 http://rdf.ncbi.nlm.nih.gov/pubchem/author/ORCID_0000-0002-8956-2207 http://rdf.ncbi.nlm.nih.gov/pubchem/author/ORCID_0000-0002-4115-9806 http://rdf.ncbi.nlm.nih.gov/pubchem/author/MD5_5ad26865d003bd609c843fa722a2e06b http://rdf.ncbi.nlm.nih.gov/pubchem/author/MD5_cb8baa0b0c8db00f46e07c053f9f8b6f http://rdf.ncbi.nlm.nih.gov/pubchem/author/MD5_6ca1bd58f38a61b575a725f89aca66ae http://rdf.ncbi.nlm.nih.gov/pubchem/author/ORCID_0000-0002-5999-5300 http://rdf.ncbi.nlm.nih.gov/pubchem/author/MD5_175b72cd2e63d47ec862269f11148341 http://rdf.ncbi.nlm.nih.gov/pubchem/author/MD5_f799f0ed5a8fb0e66ed3c0cbeec1f172 http://rdf.ncbi.nlm.nih.gov/pubchem/author/ORCID_0000-0002-9789-3591 http://rdf.ncbi.nlm.nih.gov/pubchem/author/MD5_3ff6b6ac1fcdd04f635fd5e0e970108a http://rdf.ncbi.nlm.nih.gov/pubchem/author/MD5_a1fe7a9bae46320c170c50ffac77a9a8 http://rdf.ncbi.nlm.nih.gov/pubchem/author/MD5_18c511945070b5ddb53a9e513738f56e http://rdf.ncbi.nlm.nih.gov/pubchem/author/MD5_0fd7432669e3183ad13dfc234f06b31d http://rdf.ncbi.nlm.nih.gov/pubchem/author/MD5_8f7742138758c8b515a76a980a26b989 http://rdf.ncbi.nlm.nih.gov/pubchem/author/MD5_1496f5af1a4dd7b37a3a5fda304e618a
date	2016-06-29-04:00^^<http://www.w3.org/2001/XMLSchema#date>
identifier	https://doi.org/10.1136/jmedgenet-2016-103774 https://pubmed.ncbi.nlm.nih.gov/27358179
isPartOf	https://portal.issn.org/resource/ISSN/0022-2593 http://rdf.ncbi.nlm.nih.gov/pubchem/journal/4945 https://portal.issn.org/resource/ISSN/1468-6244
language	English
source	https://pubmed.ncbi.nlm.nih.gov/ https://www.crossref.org/
title	Mutations inMYT1, encoding the myelin transcription factor 1, are a rare cause of OAVS
discussesAsDerivedByTextMining	http://rdf.ncbi.nlm.nih.gov/pubchem/compound/CID5476374 http://rdf.ncbi.nlm.nih.gov/pubchem/gene/MD5_75b1cb2b3111061c7bf9fd1929c12890 http://rdf.ncbi.nlm.nih.gov/pubchem/compound/CID444795 http://rdf.ncbi.nlm.nih.gov/pubchem/gene/MD5_4997bf895c5c365d82e65bacb20bfb83 http://rdf.ncbi.nlm.nih.gov/pubchem/disease/DZID7866 http://rdf.ncbi.nlm.nih.gov/pubchem/disease/DZID8600 http://rdf.ncbi.nlm.nih.gov/pubchem/disease/DZID7671 http://rdf.ncbi.nlm.nih.gov/pubchem/disease/DZID7277

Incoming Links

Predicate	Subject
isDiscussedBy	http://rdf.ncbi.nlm.nih.gov/pubchem/gene/GID557002 http://rdf.ncbi.nlm.nih.gov/pubchem/gene/GID140616 http://rdf.ncbi.nlm.nih.gov/pubchem/gene/GID100536821 http://rdf.ncbi.nlm.nih.gov/pubchem/gene/GID336612

Total number of triples: 49.