http://rdf.ncbi.nlm.nih.gov/pubchem/reference/22883167

Outgoing Links

Predicate Object
contentType Case Reports|Journal Article
endingPage 77
issn 0920-1211
pageRange 72-77
publicationName Epilepsy Research
startingPage 72
bibliographicCitation Poulat AL, Ville D, de Bellescize J, André-Obadia N, Cacciagli P, Milh M, Villard L, Lesca G. Homozygous TBC1D24 mutation in two siblings with familial infantile myoclonic epilepsy (FIME) and moderate intellectual disability. Epilepsy Res. 2015 Mar;111():72–7. doi: 10.1016/j.eplepsyres.2015.01.008. PMID: 25769375.
creator http://rdf.ncbi.nlm.nih.gov/pubchem/author/MD5_079c5d02f72ec18f304c6aac6d693512
http://rdf.ncbi.nlm.nih.gov/pubchem/author/MD5_f5d31a6ccc2ff251e153e95eb6640c7f
http://rdf.ncbi.nlm.nih.gov/pubchem/author/MD5_6ebcbb980ace5c557eead89c010d114f
http://rdf.ncbi.nlm.nih.gov/pubchem/author/ORCID_0000-0001-7691-9492
http://rdf.ncbi.nlm.nih.gov/pubchem/author/ORCID_0000-0001-6657-5008
http://rdf.ncbi.nlm.nih.gov/pubchem/author/MD5_c0c13dfb6dd05339d466da7cbe40f7f2
http://rdf.ncbi.nlm.nih.gov/pubchem/author/MD5_84bb7da11dc0fb2c300594d9ea4b119f
http://rdf.ncbi.nlm.nih.gov/pubchem/author/MD5_3196c58e021a899e671573b5831c77ab
http://rdf.ncbi.nlm.nih.gov/pubchem/author/MD5_90d779edbf1da11bee061ad98e23c1d3
http://rdf.ncbi.nlm.nih.gov/pubchem/author/MD5_3b7e3862583ca158ec1e7900db23852e
date 201503
identifier https://doi.org/10.1016/j.eplepsyres.2015.01.008
https://pubmed.ncbi.nlm.nih.gov/25769375
isPartOf http://rdf.ncbi.nlm.nih.gov/pubchem/journal/3587
https://portal.issn.org/resource/ISSN/0920-1211
language English
source https://www.crossref.org/
https://pubmed.ncbi.nlm.nih.gov/
title Homozygous TBC1D24 mutation in two siblings with familial infantile myoclonic epilepsy (FIME) and moderate intellectual disability
discusses http://id.nlm.nih.gov/mesh/M0014664
http://id.nlm.nih.gov/mesh/M0013341
http://id.nlm.nih.gov/mesh/M0003559
http://id.nlm.nih.gov/mesh/M0328198
http://id.nlm.nih.gov/mesh/M0550442
hasPrimarySubjectTerm http://id.nlm.nih.gov/mesh/D004831Q000235
http://id.nlm.nih.gov/mesh/D008607Q000503
http://id.nlm.nih.gov/mesh/D008607Q000235
http://id.nlm.nih.gov/mesh/D004831Q000503
http://id.nlm.nih.gov/mesh/D020125
http://id.nlm.nih.gov/mesh/D002352Q000235
hasSubjectTerm http://id.nlm.nih.gov/mesh/D002675
http://id.nlm.nih.gov/mesh/D009419
http://id.nlm.nih.gov/mesh/D010375
http://id.nlm.nih.gov/mesh/D008607Q000473
http://id.nlm.nih.gov/mesh/D004351
http://id.nlm.nih.gov/mesh/D006801
http://id.nlm.nih.gov/mesh/D008297
http://id.nlm.nih.gov/mesh/D006225Q000473
http://id.nlm.nih.gov/mesh/D004831Q000473
http://id.nlm.nih.gov/mesh/D020690
http://id.nlm.nih.gov/mesh/D008565
http://id.nlm.nih.gov/mesh/D002648
http://id.nlm.nih.gov/mesh/D035781
http://id.nlm.nih.gov/mesh/D001921Q000503
http://id.nlm.nih.gov/mesh/D004569
http://id.nlm.nih.gov/mesh/D005145Q000473
discussesAsDerivedByTextMining http://rdf.ncbi.nlm.nih.gov/pubchem/disease/DZID2641
http://rdf.ncbi.nlm.nih.gov/pubchem/gene/MD5_8b62ee3270896384ae41d936585e99bd
http://rdf.ncbi.nlm.nih.gov/pubchem/disease/DZID6462
http://rdf.ncbi.nlm.nih.gov/pubchem/disease/DZID9191
http://rdf.ncbi.nlm.nih.gov/pubchem/disease/DZID8474
http://rdf.ncbi.nlm.nih.gov/pubchem/disease/DZID8566
http://rdf.ncbi.nlm.nih.gov/pubchem/disease/DZID7621
http://rdf.ncbi.nlm.nih.gov/pubchem/disease/DZID7617
http://rdf.ncbi.nlm.nih.gov/pubchem/disease/DZID7095
http://rdf.ncbi.nlm.nih.gov/pubchem/disease/DZID9539

Total number of triples: 63.