reference/25110074

http://rdf.ncbi.nlm.nih.gov/pubchem/reference/25110074

Outgoing Links

Predicate	Object
contentType	Journal Article\|Research Support, Non-U.S. Gov't
endingPage	2470
issn	0006-8950 1460-2156
issueIdentifier	8
pageRange	2457-2470
publicationName	Brain : a journal of neurology
startingPage	2457
hasFundingAgency	http://rdf.ncbi.nlm.nih.gov/pubchem/organization/MD5_454b72a572e514d3c9f8082056407300 http://rdf.ncbi.nlm.nih.gov/pubchem/organization/MD5_487baf6554eb36bb22c6138d90a7c50f http://rdf.ncbi.nlm.nih.gov/pubchem/organization/MD5_7ae88100ecf50b03d1a9926d6373cde2
bibliographicCitation	Dong HL, Ma Y, Yu H, Wei Q, Li JQ, Liu GL, Li HF, Chen L, Chen DF, Bai G, Wu ZY. Bi-allelic loss of function variants in COX20 gene cause autosomal recessive sensory neuronopathy. Brain. 2021 Sep 04;144(8):2457–70. doi: 10.1093/brain/awab135. PMID: 33751098.
creator	http://rdf.ncbi.nlm.nih.gov/pubchem/author/MD5_f90ceb0f29b5e4a0cabbc1a0efdbf8ff http://rdf.ncbi.nlm.nih.gov/pubchem/author/MD5_e99d528d862624617a20cb136413e134 http://rdf.ncbi.nlm.nih.gov/pubchem/author/MD5_4663be4536dfa7dd76e08a98fe67cf2c http://rdf.ncbi.nlm.nih.gov/pubchem/author/MD5_0c6721faeea663fb199d77454bb8a0bd http://rdf.ncbi.nlm.nih.gov/pubchem/author/MD5_29fe0471000b7f7d4c778af8fe2854e5 http://rdf.ncbi.nlm.nih.gov/pubchem/author/MD5_3262cea0a1ae6e10c3612b8ef7092f99 http://rdf.ncbi.nlm.nih.gov/pubchem/author/MD5_a4465051655cabe9cbd863999723e03a http://rdf.ncbi.nlm.nih.gov/pubchem/author/MD5_15552c9620a437059ac5c8cce700ed36 http://rdf.ncbi.nlm.nih.gov/pubchem/author/ORCID_0000-0003-2106-572X http://rdf.ncbi.nlm.nih.gov/pubchem/author/MD5_a416eac8d2768f4bb0fa3fd7b1e439fe http://rdf.ncbi.nlm.nih.gov/pubchem/author/MD5_ee80cda559f3fb14bff352fd3fdeda17
date	2021-03-22-04:00^^<http://www.w3.org/2001/XMLSchema#date>
identifier	https://doi.org/10.1093/brain/awab135 https://pubmed.ncbi.nlm.nih.gov/33751098
isPartOf	https://portal.issn.org/resource/ISSN/0006-8950 https://portal.issn.org/resource/ISSN/1460-2156 http://rdf.ncbi.nlm.nih.gov/pubchem/journal/1917
language	English
source	https://pubmed.ncbi.nlm.nih.gov/ https://www.crossref.org/
title	Bi-allelic loss of function variants in COX20 gene cause autosomal recessive sensory neuronopathy
discusses	http://id.nlm.nih.gov/mesh/M0005587 http://id.nlm.nih.gov/mesh/M000601362
hasPrimarySubjectTerm	http://id.nlm.nih.gov/mesh/D030401Q000235 http://id.nlm.nih.gov/mesh/D009477Q000235 http://id.nlm.nih.gov/mesh/D003576Q000235 http://id.nlm.nih.gov/mesh/D008928Q000235 http://id.nlm.nih.gov/mesh/D019656
hasSubjectTerm	http://id.nlm.nih.gov/mesh/D008297 http://id.nlm.nih.gov/mesh/D000293 http://id.nlm.nih.gov/mesh/D002648 http://id.nlm.nih.gov/mesh/D014459Q000503 http://id.nlm.nih.gov/mesh/D009431Q000502 http://id.nlm.nih.gov/mesh/D002675 http://id.nlm.nih.gov/mesh/D000328 http://id.nlm.nih.gov/mesh/D011826Q000503 http://id.nlm.nih.gov/mesh/D009477Q000503 http://id.nlm.nih.gov/mesh/D030401Q000503 http://id.nlm.nih.gov/mesh/D005260 http://id.nlm.nih.gov/mesh/D010375 http://id.nlm.nih.gov/mesh/D008475Q000503 http://id.nlm.nih.gov/mesh/D049109Q000235 http://id.nlm.nih.gov/mesh/D006801 http://id.nlm.nih.gov/mesh/D009154
discussesAsDerivedByTextMining	http://rdf.ncbi.nlm.nih.gov/pubchem/disease/DZID8936 http://rdf.ncbi.nlm.nih.gov/pubchem/gene/MD5_2c5ff4b27d9fca3d3a0c8bf968d6441c http://rdf.ncbi.nlm.nih.gov/pubchem/disease/DZID8854 http://rdf.ncbi.nlm.nih.gov/pubchem/gene/MD5_c6f5c45259f2b523c06734991169af67 http://rdf.ncbi.nlm.nih.gov/pubchem/disease/DZID10739 http://rdf.ncbi.nlm.nih.gov/pubchem/gene/MD5_2ac1c7439672b7b031bd7ba9fc373389 http://rdf.ncbi.nlm.nih.gov/pubchem/compound/CID977 http://rdf.ncbi.nlm.nih.gov/pubchem/gene/MD5_6854ebb6fabc347df9dad3e13a98d41d http://rdf.ncbi.nlm.nih.gov/pubchem/gene/MD5_e38bc58690fe76fbdc3d18f14c8e6141 http://rdf.ncbi.nlm.nih.gov/pubchem/gene/MD5_917008bd64c42e6f5ae78e7e43c0e1a5 http://rdf.ncbi.nlm.nih.gov/pubchem/disease/DZID10721 http://rdf.ncbi.nlm.nih.gov/pubchem/disease/DZID6989 http://rdf.ncbi.nlm.nih.gov/pubchem/gene/MD5_6f12f64d60439d77f0fa924189805575

Incoming Links

Predicate	Subject
isDiscussedBy	http://rdf.ncbi.nlm.nih.gov/pubchem/gene/GID116228

Total number of triples: 70.