http://rdf.ncbi.nlm.nih.gov/pubchem/reference/26427648

Outgoing Links

Predicate Object
contentType Journal Article|Research Support, Non-U.S. Gov't
endingPage 1345
issn 1531-8257
0885-3185
issueIdentifier 8
pageRange 1336-1345
publicationName Movement disorders : official journal of the Movement Disorder Society
startingPage 1336
hasFundingAgency http://rdf.ncbi.nlm.nih.gov/pubchem/organization/MD5_7975acd05863b722dccc0e179fb8efcc
http://rdf.ncbi.nlm.nih.gov/pubchem/organization/MD5_fdb95f94008cff51464e99b04994a610
bibliographicCitation Cassinari K, Rovelet‐Lecrux A, Tury S, Quenez O, Richard A, Charbonnier C, Olaso R, Boland A, Deleuze J, Besancenot J, Delpont B, Pouliquen D, Lecoquierre F, Chambon P, Thauvin‐Robinet C, Campion D, Frebourg T, Battini J, Nicolas G. Haploinsufficiency of the Primary Familial Brain Calcification Gene SLC20A2 Mediated by Disruption of a Regulatory Element. Movement Disorders. 2020 Jun 07;35(8):1336–45. doi: 10.1002/mds.28090.
creator http://rdf.ncbi.nlm.nih.gov/pubchem/author/ORCID_0000-0002-9040-3051
http://rdf.ncbi.nlm.nih.gov/pubchem/author/MD5_ae42efaed7152c3e7a7b4f9d895b74e3
http://rdf.ncbi.nlm.nih.gov/pubchem/author/MD5_d9fbfc664c98996270ee727c8ffc116a
http://rdf.ncbi.nlm.nih.gov/pubchem/author/MD5_3631a1088566d0456b65c8c636b12ce8
http://rdf.ncbi.nlm.nih.gov/pubchem/author/MD5_e5739f5d83c42e71b0c7ceb2160f5947
http://rdf.ncbi.nlm.nih.gov/pubchem/author/ORCID_0000-0001-9391-7800
http://rdf.ncbi.nlm.nih.gov/pubchem/author/MD5_34396fefa685aa9c39b2c4324110bcd8
http://rdf.ncbi.nlm.nih.gov/pubchem/author/MD5_9d795efdc8ed7867b7763b7a5d2bd019
http://rdf.ncbi.nlm.nih.gov/pubchem/author/MD5_e8a46ba5e95d7c38f7005a871e38bcc4
http://rdf.ncbi.nlm.nih.gov/pubchem/author/MD5_4f0eb2bf3eb24dd930db3d45a774f68a
http://rdf.ncbi.nlm.nih.gov/pubchem/author/MD5_790b73af26f043b95415db4819fbbc3a
http://rdf.ncbi.nlm.nih.gov/pubchem/author/MD5_dd3d83143a351dabc11fde10751a2ba0
http://rdf.ncbi.nlm.nih.gov/pubchem/author/MD5_529a803c130cb18e48ee7b0fa2a042ca
http://rdf.ncbi.nlm.nih.gov/pubchem/author/ORCID_0000-0003-2683-4073
http://rdf.ncbi.nlm.nih.gov/pubchem/author/MD5_008dc2c551af6f263b550d1fad9b2234
http://rdf.ncbi.nlm.nih.gov/pubchem/author/ORCID_0000-0001-9291-734X
http://rdf.ncbi.nlm.nih.gov/pubchem/author/MD5_6e9ae40a546fca4dba080c52b5b11091
http://rdf.ncbi.nlm.nih.gov/pubchem/author/MD5_999c7d1b7e23207c46ecd2b1c1f80d17
http://rdf.ncbi.nlm.nih.gov/pubchem/author/MD5_b8825e58b561b47e3de7ea186392bf49
http://rdf.ncbi.nlm.nih.gov/pubchem/author/MD5_70aed1948bedc4b02875e98f4a6db522
http://rdf.ncbi.nlm.nih.gov/pubchem/author/MD5_09c53a0ba8b753f9c12af9af0d883888
date 2020-06-07-04:00^^<http://www.w3.org/2001/XMLSchema#date>
identifier https://doi.org/10.1002/mds.28090
https://pubmed.ncbi.nlm.nih.gov/32506582
isPartOf https://portal.issn.org/resource/ISSN/0885-3185
https://portal.issn.org/resource/ISSN/1531-8257
http://rdf.ncbi.nlm.nih.gov/pubchem/journal/5937
language English
source https://pubmed.ncbi.nlm.nih.gov/
https://www.crossref.org/
title Haploinsufficiency of the Primary Familial Brain Calcification Gene SLC20A2 Mediated by Disruption of a Regulatory Element
discusses http://id.nlm.nih.gov/mesh/M0371702
http://id.nlm.nih.gov/mesh/M0438815
hasPrimarySubjectTerm http://id.nlm.nih.gov/mesh/D001927
http://id.nlm.nih.gov/mesh/D050611Q000235
hasSubjectTerm http://id.nlm.nih.gov/mesh/D056915
http://id.nlm.nih.gov/mesh/D006801
http://id.nlm.nih.gov/mesh/D057895Q000235
http://id.nlm.nih.gov/mesh/D009154Q000235
http://id.nlm.nih.gov/mesh/D001921Q000378
http://id.nlm.nih.gov/mesh/D057809
discussesAsDerivedByTextMining http://rdf.ncbi.nlm.nih.gov/pubchem/disease/DZID7136
http://rdf.ncbi.nlm.nih.gov/pubchem/protein/EC_2.7.7.49
http://rdf.ncbi.nlm.nih.gov/pubchem/gene/MD5_9189c00b631b9f16d933cea94ca3ac0d
http://rdf.ncbi.nlm.nih.gov/pubchem/disease/DZID8805
http://rdf.ncbi.nlm.nih.gov/pubchem/disease/DZID8519

Incoming Links

Predicate Subject
isDiscussedBy http://rdf.ncbi.nlm.nih.gov/pubchem/gene/GID6575

Total number of triples: 58.