http://rdf.ncbi.nlm.nih.gov/pubchem/reference/17541323

Outgoing Links

Predicate Object
contentType Journal Article
endingPage 709
issn 0366-6999
issueIdentifier 6
pageRange 703-709
publicationName Chinese Medical Journal
startingPage 703
bibliographicCitation Wang L, Lin QF, Wang HY, Guan J, Lan L, Xie LY, Yu L, Yang J, Zhao C, Liang JL, Zhou HL, Yang HM, Xiong WP, Zhang QJ, Wang DY, Wang QJ. Clinical Auditory Phenotypes Associated with GATA3 Gene Mutations in Familial Hypoparathyroidism-deafness-renal Dysplasia Syndrome. Chin Med J (Engl). 2017 Mar 20;130(6):703–9. PMID: 28303854; PMCID: PMC5358421.
creator http://rdf.ncbi.nlm.nih.gov/pubchem/author/MD5_8bede2a27240e172088458142d6ec4a3
http://rdf.ncbi.nlm.nih.gov/pubchem/author/MD5_ced93a4e3333bf2a27853afee7a017e8
http://rdf.ncbi.nlm.nih.gov/pubchem/author/MD5_8105450c17dd293d07dfd7d7bcc92bcb
http://rdf.ncbi.nlm.nih.gov/pubchem/author/MD5_a050783804b086f3c4fb283052ebeccd
http://rdf.ncbi.nlm.nih.gov/pubchem/author/MD5_e7eaba3eb70f79ae162d5aee4be0a9a8
http://rdf.ncbi.nlm.nih.gov/pubchem/author/MD5_765c9842c77c0a907e73ff01a4d5d566
http://rdf.ncbi.nlm.nih.gov/pubchem/author/MD5_005c2748c2e2c7443cc3da502f7dac1f
http://rdf.ncbi.nlm.nih.gov/pubchem/author/MD5_f85df80575df5432bd59b05a7321ff22
http://rdf.ncbi.nlm.nih.gov/pubchem/author/MD5_9b39a7fe2609331dcb6a6fdf6fd5a2e1
http://rdf.ncbi.nlm.nih.gov/pubchem/author/MD5_9b87b35c8ca8ff051e136ceb44725f42
http://rdf.ncbi.nlm.nih.gov/pubchem/author/MD5_b0d641e921466abf17a467f51d056c0d
http://rdf.ncbi.nlm.nih.gov/pubchem/author/MD5_23c5516852c8530522cb5ef2f0401005
http://rdf.ncbi.nlm.nih.gov/pubchem/author/MD5_2f45d68802652de7cc21f62a12b1d013
http://rdf.ncbi.nlm.nih.gov/pubchem/author/MD5_8445a4b25ff207a1e1e1b9cbd736a138
http://rdf.ncbi.nlm.nih.gov/pubchem/author/MD5_72ab6fb2c59d38b1434bd69f88fd038e
http://rdf.ncbi.nlm.nih.gov/pubchem/author/MD5_1787f4e03e2f6db73b39e6e2750e7fdc
date 2017-03-20-04:00^^<http://www.w3.org/2001/XMLSchema#date>
identifier https://pubmed.ncbi.nlm.nih.gov/28303854
https://doi.org/10.4103/0366-6999.201600
https://pubmed.ncbi.nlm.nih.gov/PMC5358421
isPartOf https://portal.issn.org/resource/ISSN/0366-6999
http://rdf.ncbi.nlm.nih.gov/pubchem/journal/2927
language English
source https://www.crossref.org/
https://pubmed.ncbi.nlm.nih.gov/
title Clinical Auditory Phenotypes Associated with GATA3 Gene Mutations in Familial Hypoparathyroidism-deafness-renal Dysplasia Syndrome
discusses http://id.nlm.nih.gov/mesh/C537907
http://id.nlm.nih.gov/mesh/M0187088
http://id.nlm.nih.gov/mesh/M0187089
hasPrimarySubjectTerm http://id.nlm.nih.gov/mesh/D007011Q000235
http://id.nlm.nih.gov/mesh/D050990Q000235
http://id.nlm.nih.gov/mesh/D009401Q000235
http://id.nlm.nih.gov/mesh/D006319Q000235
hasSubjectTerm http://id.nlm.nih.gov/mesh/D002648
http://id.nlm.nih.gov/mesh/D059014
http://id.nlm.nih.gov/mesh/D005260
http://id.nlm.nih.gov/mesh/D009154Q000235
http://id.nlm.nih.gov/mesh/D034381Q000235
http://id.nlm.nih.gov/mesh/D010375
http://id.nlm.nih.gov/mesh/D005838
http://id.nlm.nih.gov/mesh/D006801
http://id.nlm.nih.gov/mesh/D008297
discussesAsDerivedByTextMining http://rdf.ncbi.nlm.nih.gov/pubchem/disease/DZID7391
http://rdf.ncbi.nlm.nih.gov/pubchem/gene/MD5_1a9fd16e4a9ee3ac7708efecfbed0c0d
http://rdf.ncbi.nlm.nih.gov/pubchem/disease/DZID8118
http://rdf.ncbi.nlm.nih.gov/pubchem/disease/DZID10757
http://rdf.ncbi.nlm.nih.gov/pubchem/disease/DZID8127
http://rdf.ncbi.nlm.nih.gov/pubchem/disease/DZID10689
http://rdf.ncbi.nlm.nih.gov/pubchem/disease/DZID7915
http://rdf.ncbi.nlm.nih.gov/pubchem/disease/DZID2388

Incoming Links

Predicate Subject
isDiscussedBy http://rdf.ncbi.nlm.nih.gov/pubchem/gene/GID2625

Total number of triples: 59.