reference/1929059

http://rdf.ncbi.nlm.nih.gov/pubchem/reference/1929059

Outgoing Links

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contentType	Case Reports\|Journal Article\|Research Support, Non-U.S. Gov't
issn	1471-2350
issueIdentifier	1
pageRange	88-
publicationName	BMC Medical Genetics
startingPage	88
hasFundingAgency	http://rdf.ncbi.nlm.nih.gov/pubchem/organization/MD5_2613a34394c0f21a5a0601254003db93 http://rdf.ncbi.nlm.nih.gov/pubchem/organization/MD5_a310404787eabec4feb636cd8219794e http://rdf.ncbi.nlm.nih.gov/pubchem/organization/MD5_a13fca660c294781518ea3acad4523d4 http://rdf.ncbi.nlm.nih.gov/pubchem/organization/MD5_487baf6554eb36bb22c6138d90a7c50f
bibliographicCitation	Wang P, Cai F, Cao L, Wang Y, Zou Q, Zhao P, Wang C, Zhang Y, Cai C, Shu J. Clinical diagnosis and mutation analysis of four Chinese families with succinic semialdehyde dehydrogenase deficiency. BMC Medical Genomics. 2019 May 22;20(1):88. doi: 10.1186/s12881-019-0821-z.
creator	http://rdf.ncbi.nlm.nih.gov/pubchem/author/MD5_49923ea9977656e7757dd21cf8d7cef5 http://rdf.ncbi.nlm.nih.gov/pubchem/author/MD5_0f6d90d4570dd4ea0a5d3b9960f1cbbd http://rdf.ncbi.nlm.nih.gov/pubchem/author/MD5_79e649a66f568f9632624f3168455897 http://rdf.ncbi.nlm.nih.gov/pubchem/author/MD5_19d8fe92ebc6342343775f507cee142b http://rdf.ncbi.nlm.nih.gov/pubchem/author/MD5_1affc45436354df74a33482488b36b27 http://rdf.ncbi.nlm.nih.gov/pubchem/author/MD5_982cdcc462aed919323df3e6cd81aefc http://rdf.ncbi.nlm.nih.gov/pubchem/author/MD5_7b9f0698f0f15afb5d577e502183a40c http://rdf.ncbi.nlm.nih.gov/pubchem/author/MD5_f50dc1d3c70ed45f75a3953f0d0e82e0 http://rdf.ncbi.nlm.nih.gov/pubchem/author/MD5_c3643893dcba1cc39a896c60dbc62ff0 http://rdf.ncbi.nlm.nih.gov/pubchem/author/ORCID_0000-0002-5903-7954
date	2019-05-22-04:00^^<http://www.w3.org/2001/XMLSchema#date>
identifier	https://pubmed.ncbi.nlm.nih.gov/PMC6532217 https://doi.org/10.1186/s12881-019-0821-z https://pubmed.ncbi.nlm.nih.gov/31117962
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language	English
source	https://scigraph.springernature.com/ https://www.crossref.org/ https://pubmed.ncbi.nlm.nih.gov/
title	Clinical diagnosis and mutation analysis of four Chinese families with succinic semialdehyde dehydrogenase deficiency
discusses	http://id.nlm.nih.gov/mesh/C535803 http://id.nlm.nih.gov/mesh/M0079133
discussesAsDerivedByTextMining	http://rdf.ncbi.nlm.nih.gov/pubchem/disease/DZID7617 http://rdf.ncbi.nlm.nih.gov/pubchem/disease/DZID608 http://rdf.ncbi.nlm.nih.gov/pubchem/compound/CID5892 http://rdf.ncbi.nlm.nih.gov/pubchem/compound/CID10413 http://rdf.ncbi.nlm.nih.gov/pubchem/disease/DZID9191 http://rdf.ncbi.nlm.nih.gov/pubchem/compound/CID119

Incoming Links

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Total number of triples: 41.