reference/14920670

http://rdf.ncbi.nlm.nih.gov/pubchem/reference/14920670

Outgoing Links

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contentType	Journal Article\|Research Support, Non-U.S. Gov't
issn	1750-1172
issueIdentifier	1
pageRange	74-
publicationName	Orphanet Journal of Rare Diseases
startingPage	74
hasFundingAgency	http://rdf.ncbi.nlm.nih.gov/pubchem/organization/MD5_31201572dc616582982a6d7867d67afa
bibliographicCitation	Wu L, Li Y, Song Y, Zhou D, Jia S, Xu A, Zhang W, You H, Jia J, Huang J, Ou X. A recurrent ABCC2 p.G693R mutation resulting in loss of function of MRP2 and hyperbilirubinemia in Dubin-Johnson syndrome in China. Orphanet Journal of Rare Diseases. 2020 Mar 18;15(1):74. doi: 10.1186/s13023-020-1346-4.
creator	http://rdf.ncbi.nlm.nih.gov/pubchem/author/MD5_5d825f5efdd8f873821082b60a83b920 http://rdf.ncbi.nlm.nih.gov/pubchem/author/MD5_16ecb72cabfebc0d42ce248929e5d237 http://rdf.ncbi.nlm.nih.gov/pubchem/author/ORCID_0000-0002-3220-6041 http://rdf.ncbi.nlm.nih.gov/pubchem/author/MD5_68417e120917831f9147890f374bc060 http://rdf.ncbi.nlm.nih.gov/pubchem/author/MD5_ad04da849285e8aa6f32dfa1171531f0 http://rdf.ncbi.nlm.nih.gov/pubchem/author/MD5_66a0eff99d9e77db324961ba30647a70 http://rdf.ncbi.nlm.nih.gov/pubchem/author/MD5_1f48936506f770f454cdebc094c61b6d http://rdf.ncbi.nlm.nih.gov/pubchem/author/MD5_a427691ce32a2d37578809548802eda7 http://rdf.ncbi.nlm.nih.gov/pubchem/author/MD5_93e5902f93d32949b108f52247e7f0ff http://rdf.ncbi.nlm.nih.gov/pubchem/author/MD5_ee782b70a0d45ca3cbe6691153be9285 http://rdf.ncbi.nlm.nih.gov/pubchem/author/MD5_3db16353862347663eb7748ed73c7991
date	2020-03-18-04:00^^<http://www.w3.org/2001/XMLSchema#date>
identifier	https://doi.org/10.1186/s13023-020-1346-4 https://pubmed.ncbi.nlm.nih.gov/PMC7079413 https://pubmed.ncbi.nlm.nih.gov/32183854
isPartOf	http://rdf.ncbi.nlm.nih.gov/pubchem/journal/32787 https://portal.issn.org/resource/ISSN/1750-1172
language	English
source	https://pubmed.ncbi.nlm.nih.gov/ https://scigraph.springernature.com/ https://www.crossref.org/
title	A recurrent ABCC2 p.G693R mutation resulting in loss of function of MRP2 and hyperbilirubinemia in Dubin-Johnson syndrome in China
discusses	http://id.nlm.nih.gov/mesh/M0304794 http://id.nlm.nih.gov/mesh/M000744925 http://id.nlm.nih.gov/mesh/M0238823
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Incoming Links

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isDiscussedBy	http://rdf.ncbi.nlm.nih.gov/pubchem/gene/GID1244

Total number of triples: 41.