reference/20978073

http://rdf.ncbi.nlm.nih.gov/pubchem/reference/20978073

Outgoing Links

Predicate	Object
contentType	Journal Article
endingPage	239
issn	2473-4039
issueIdentifier	4
pageRange	235-239
publicationName	JBMR Plus
startingPage	235
hasFundingAgency	http://rdf.ncbi.nlm.nih.gov/pubchem/organization/MD5_bbe1ab52cb3b85124386d12499e4bc70 http://rdf.ncbi.nlm.nih.gov/pubchem/organization/MD5_c764e516438dcf501912b31b60668d3c
bibliographicCitation	Jin Z, Burrage LC, Jiang MM, Lee YC, Bertin T, Chen Y, Tran A, Gibbs RA, Jhangiani S, Sutton VR, Rauch F, Lee B, Jain M. Whole-Exome Sequencing Identifies an Intronic Cryptic Splice Site in SERPINF1 Causing Osteogenesis Imperfecta Type VI. JBMR Plus. 2018 Jul;2(4):235–9. PMID: 30283904; PMCID: PMC6124173.
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date	2018-04-16-04:00^^<http://www.w3.org/2001/XMLSchema#date>
identifier	https://doi.org/10.1002/jbm4.10044 https://pubmed.ncbi.nlm.nih.gov/30283904 https://pubmed.ncbi.nlm.nih.gov/PMC6124173
isPartOf	https://portal.issn.org/resource/ISSN/2473-4039 http://rdf.ncbi.nlm.nih.gov/pubchem/journal/46632
language	English
source	https://pubmed.ncbi.nlm.nih.gov/ https://www.crossref.org/
title	Whole‐Exome Sequencing Identifies an Intronic Cryptic Splice Site in SERPINF1 Causing Osteogenesis Imperfecta Type VI
discussesAsDerivedByTextMining	http://rdf.ncbi.nlm.nih.gov/pubchem/compound/CID11575713 http://rdf.ncbi.nlm.nih.gov/pubchem/gene/MD5_2c404b18dfdff6dd7b9702f960d8021c http://rdf.ncbi.nlm.nih.gov/pubchem/disease/DZID7073 http://rdf.ncbi.nlm.nih.gov/pubchem/disease/DZID8728

Total number of triples: 37.