reference/33113525

http://rdf.ncbi.nlm.nih.gov/pubchem/reference/33113525

Outgoing Links

Predicate	Object
contentType	Case Reports\|Journal Article
endingPage	1252
issn	1720-8386 0391-4097
issueIdentifier	10
pageRange	1245-1252
publicationName	Journal of Endocrinological Investigation
startingPage	1245
hasFundingAgency	http://rdf.ncbi.nlm.nih.gov/pubchem/organization/MD5_687c9581d8a0a5252d37acb4b8e0459f http://rdf.ncbi.nlm.nih.gov/pubchem/organization/MD5_e262c48f6ed47e62f7179020d1d6c1bd http://rdf.ncbi.nlm.nih.gov/pubchem/organization/MD5_9594bc245e01d5e698b204bc6c70bd47 http://rdf.ncbi.nlm.nih.gov/pubchem/organization/MD5_c04fd0c1eda847c5e722e761bd859dc8 http://rdf.ncbi.nlm.nih.gov/pubchem/organization/MD5_1e75a8d80bde809a0192174998e32895 http://rdf.ncbi.nlm.nih.gov/pubchem/organization/MD5_824fdfd9ad4b59fa9a1f922da82b3a1f http://rdf.ncbi.nlm.nih.gov/pubchem/organization/MD5_4f20d94a067228244ce86970b3140668 http://rdf.ncbi.nlm.nih.gov/pubchem/organization/MD5_ccd53193d8522144294cf7264974b051 http://rdf.ncbi.nlm.nih.gov/pubchem/organization/MD5_1bd0a80f5e5e140c82e2bfb672a20aea http://rdf.ncbi.nlm.nih.gov/pubchem/organization/MD5_f4ff9db53ce62a992e8983508fba5eba http://rdf.ncbi.nlm.nih.gov/pubchem/organization/MD5_e9a9aa23b6f0215d1149c858ca874d52 http://rdf.ncbi.nlm.nih.gov/pubchem/organization/MD5_eb213a5fd6d26b5cdde592757803b89f http://rdf.ncbi.nlm.nih.gov/pubchem/organization/MD5_f7e2a29e7d44f9d749b69300b5e13853 http://rdf.ncbi.nlm.nih.gov/pubchem/organization/MD5_71f4b76a18040ac36a51bcb8296c799c
bibliographicCitation	Jiang Y, Du J, Song Y-, Wang W-, Pang Q-, Li M, Wang O, Lian X-, Xing X-, Xia W-. Novel SLCO2A1compound heterozygous mutation causing primary hypertrophic osteoarthropathy with Bartter-like hypokalemia in a Chinese family. Journal of Endocrinological Investigation. 2019 Apr 19;42(10):1245–52. doi: 10.1007/s40618-019-01048-z.
creator	http://rdf.ncbi.nlm.nih.gov/pubchem/author/MD5_020d2de1f654362adb8bbcdd5a59f53a http://rdf.ncbi.nlm.nih.gov/pubchem/author/MD5_0f518cac372b8a882acfddec295a32e3 http://rdf.ncbi.nlm.nih.gov/pubchem/author/MD5_96d1cf7eb14359de8b135622c45f7608 http://rdf.ncbi.nlm.nih.gov/pubchem/author/MD5_5fadba0eb1f97b781e7a8e741ca51806 http://rdf.ncbi.nlm.nih.gov/pubchem/author/MD5_f922f5023548df3ebf96ca8237f2e3fb http://rdf.ncbi.nlm.nih.gov/pubchem/author/MD5_9f54ca4bd75ec7f2b74682ea6376a966 http://rdf.ncbi.nlm.nih.gov/pubchem/author/MD5_4fa6a9edd2bfa8fedcd92c5917b2cd10 http://rdf.ncbi.nlm.nih.gov/pubchem/author/MD5_51e6094fd49fb69481aa6464e7548b2b http://rdf.ncbi.nlm.nih.gov/pubchem/author/ORCID_0000-0003-4434-3462 http://rdf.ncbi.nlm.nih.gov/pubchem/author/MD5_a300547aef9b85ad80230d6ac089b6ce
date	2019-04-19-04:00^^<http://www.w3.org/2001/XMLSchema#date>
identifier	https://doi.org/10.1007/s40618-019-01048-z https://pubmed.ncbi.nlm.nih.gov/31004291
isPartOf	http://rdf.ncbi.nlm.nih.gov/pubchem/journal/4766 https://portal.issn.org/resource/ISSN/1720-8386 https://portal.issn.org/resource/ISSN/0391-4097
language	English
source	https://scigraph.springernature.com/ https://www.crossref.org/ https://pubmed.ncbi.nlm.nih.gov/
title	Novel SLCO2A1compound heterozygous mutation causing primary hypertrophic osteoarthropathy with Bartter-like hypokalemia in a Chinese family
discusses	http://id.nlm.nih.gov/mesh/M0488971 http://id.nlm.nih.gov/mesh/M0076804
discussesAsDerivedByTextMining	http://rdf.ncbi.nlm.nih.gov/pubchem/gene/MD5_2aa3a5835854786d8310663cf445351c http://rdf.ncbi.nlm.nih.gov/pubchem/disease/DZID7554 http://rdf.ncbi.nlm.nih.gov/pubchem/compound/CID123619 http://rdf.ncbi.nlm.nih.gov/pubchem/disease/DZID8124 http://rdf.ncbi.nlm.nih.gov/pubchem/compound/CID5280360 http://rdf.ncbi.nlm.nih.gov/pubchem/compound/CID5462222 http://rdf.ncbi.nlm.nih.gov/pubchem/compound/CID5280711 http://rdf.ncbi.nlm.nih.gov/pubchem/disease/DZID10737 http://rdf.ncbi.nlm.nih.gov/pubchem/disease/DZID8723 http://rdf.ncbi.nlm.nih.gov/pubchem/gene/MD5_afc3d213613bf1e2bf8b4ffeedd58ae0

Incoming Links

Predicate	Subject
isDiscussedBy	http://rdf.ncbi.nlm.nih.gov/pubchem/gene/GID6578

Total number of triples: 57.