reference/435736

http://rdf.ncbi.nlm.nih.gov/pubchem/reference/435736

Outgoing Links

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contentType	Journal Article\|Research Support, Non-U.S. Gov't
issn	1750-1172
issueIdentifier	1
pageRange	10-
publicationName	Orphanet Journal of Rare Diseases
startingPage	10
bibliographicCitation	Salsano E, Tabano S, Sirchia SM, Colapietro P, Castellotti B, Gellera C, Rimoldi M, Pensato V, Mariotti C, Pareyson D, Miozzo M, Uziel G. Preferential expression of mutant ABCD1 allele is common in adrenoleukodystrophy female carriers but unrelated to clinical symptoms. Orphanet Journal of Rare Diseases. 2012 Jan 26;7(1):10. doi: 10.1186/1750-1172-7-10.
creator	http://rdf.ncbi.nlm.nih.gov/pubchem/author/MD5_bf57472aa81586b01ad9727c0e102eb8 http://rdf.ncbi.nlm.nih.gov/pubchem/author/MD5_d8129c546d904252a380f08eb4bf764b http://rdf.ncbi.nlm.nih.gov/pubchem/author/ORCID_0000-0001-6854-765X http://rdf.ncbi.nlm.nih.gov/pubchem/author/MD5_b90acc167ba052c448617a681a0e9222 http://rdf.ncbi.nlm.nih.gov/pubchem/author/MD5_483a1dde2c6cea09943b5ba71acfc0f1 http://rdf.ncbi.nlm.nih.gov/pubchem/author/ORCID_0000-0002-9098-3041 http://rdf.ncbi.nlm.nih.gov/pubchem/author/MD5_f7fe89770a524b7567ba01487bd7b0fc http://rdf.ncbi.nlm.nih.gov/pubchem/author/ORCID_0000-0002-3582-665X http://rdf.ncbi.nlm.nih.gov/pubchem/author/ORCID_0000-0001-9167-1878 http://rdf.ncbi.nlm.nih.gov/pubchem/author/ORCID_0000-0001-9798-2669 http://rdf.ncbi.nlm.nih.gov/pubchem/author/MD5_c41df7f26ba1cb5072d6d7a82cf8c23d http://rdf.ncbi.nlm.nih.gov/pubchem/author/MD5_d3e1d9734ea0f3f59235acd9d20b6c8f http://rdf.ncbi.nlm.nih.gov/pubchem/author/MD5_a183f2bdbe4470f0c7275420b184287b http://rdf.ncbi.nlm.nih.gov/pubchem/author/ORCID_0000-0003-2405-3564 http://rdf.ncbi.nlm.nih.gov/pubchem/author/MD5_1aea9680ab978743fb032d28d78784f1 http://rdf.ncbi.nlm.nih.gov/pubchem/author/MD5_34f60b33d4fe76a0ced415c6ffaa5186 http://rdf.ncbi.nlm.nih.gov/pubchem/author/ORCID_0000-0002-6523-4575 http://rdf.ncbi.nlm.nih.gov/pubchem/author/MD5_db06c448bedc2a400c957d453212e066 http://rdf.ncbi.nlm.nih.gov/pubchem/author/MD5_29d1c67bb7dcf42f938ccaf2893636e3
date	2012-01-26-04:00^^<http://www.w3.org/2001/XMLSchema#date>
identifier	https://doi.org/10.1186/1750-1172-7-10 https://pubmed.ncbi.nlm.nih.gov/PMC3298485 https://pubmed.ncbi.nlm.nih.gov/22280810
isPartOf	https://portal.issn.org/resource/ISSN/1750-1172 http://rdf.ncbi.nlm.nih.gov/pubchem/journal/32787
language	English
source	https://pubmed.ncbi.nlm.nih.gov/ https://scigraph.springernature.com/ https://www.crossref.org/
title	Preferential expression of mutant ABCD1 allele is common in adrenoleukodystrophy female carriers but unrelated to clinical symptoms
discusses	http://id.nlm.nih.gov/mesh/M0027776 http://id.nlm.nih.gov/mesh/M0297524 http://id.nlm.nih.gov/mesh/M000625394
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Incoming Links

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isDiscussedBy	http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID128364298 http://rdf.ncbi.nlm.nih.gov/pubchem/gene/GID215

Total number of triples: 46.