reference/13428016

http://rdf.ncbi.nlm.nih.gov/pubchem/reference/13428016

Outgoing Links

Predicate	Object
contentType	Case Reports\|Letter\|Research Support, Non-U.S. Gov't
endingPage	98
issn	0009-9163 1399-0004
issueIdentifier	1
pageRange	96-98
publicationName	Clinical Genetics
startingPage	96
hasFundingAgency	http://rdf.ncbi.nlm.nih.gov/pubchem/organization/MD5_ff75081d7fcc7f5d3b6e1cf4bd3a91ec
bibliographicCitation	Neřoldová M, Fraňková S, Stránecký V, Honsová E, Lukšan O, Beneš M, Michalová K, Kmoch S, Jirsa M. Hereditary haemochromatosis caused by homozygous HJV mutation evolved through paternal disomy. Clinical Genetics. 2014 Feb 12;87(1):96–8. doi: 10.1111/cge.12346.
creator	http://rdf.ncbi.nlm.nih.gov/pubchem/author/MD5_a58b70d8f9d8851efea9590c39236acf http://rdf.ncbi.nlm.nih.gov/pubchem/author/MD5_cd8037f9517b276368b5b57fbe713724 http://rdf.ncbi.nlm.nih.gov/pubchem/author/MD5_27b5c6f5779dcf710d524bc0e2c29b6d http://rdf.ncbi.nlm.nih.gov/pubchem/author/MD5_94e4b2fd68a60705c1d488ad8b28af25 http://rdf.ncbi.nlm.nih.gov/pubchem/author/MD5_57ca479e3b4bc7a34b7e41930651e474 http://rdf.ncbi.nlm.nih.gov/pubchem/author/MD5_b90ad7cd4d40704fc25369e57d661684 http://rdf.ncbi.nlm.nih.gov/pubchem/author/MD5_94fe2c48402e410d2906f87ec461f920 http://rdf.ncbi.nlm.nih.gov/pubchem/author/MD5_ebfbcd56e92558baea93158e1764d8c8 http://rdf.ncbi.nlm.nih.gov/pubchem/author/MD5_65e1a6897089b409df16d21346f980f2
date	2014-02-12-04:00^^<http://www.w3.org/2001/XMLSchema#date>
identifier	https://doi.org/10.1111/cge.12346 https://pubmed.ncbi.nlm.nih.gov/24635876
isPartOf	https://portal.issn.org/resource/ISSN/0009-9163 http://rdf.ncbi.nlm.nih.gov/pubchem/journal/3010 https://portal.issn.org/resource/ISSN/1399-0004
language	English
source	https://www.crossref.org/ https://pubmed.ncbi.nlm.nih.gov/
title	Hereditary haemochromatosis caused by homozygous HJV mutation evolved through paternal disomy
discusses	http://id.nlm.nih.gov/mesh/M000612938 http://id.nlm.nih.gov/mesh/M0271015 http://id.nlm.nih.gov/mesh/C537247 http://id.nlm.nih.gov/mesh/M0023721 http://id.nlm.nih.gov/mesh/M0013341
hasPrimarySubjectTerm	http://id.nlm.nih.gov/mesh/D024182Q000235 http://id.nlm.nih.gov/mesh/D006432Q000151 http://id.nlm.nih.gov/mesh/D015395Q000235 http://id.nlm.nih.gov/mesh/D008565Q000235
hasSubjectTerm	http://id.nlm.nih.gov/mesh/D006801 http://id.nlm.nih.gov/mesh/D000328 http://id.nlm.nih.gov/mesh/D012150 http://id.nlm.nih.gov/mesh/D010375 http://id.nlm.nih.gov/mesh/D008297 http://id.nlm.nih.gov/mesh/D006432Q000235 http://id.nlm.nih.gov/mesh/D000071020 http://id.nlm.nih.gov/mesh/D017422
discussesAsDerivedByTextMining	http://rdf.ncbi.nlm.nih.gov/pubchem/disease/DZID6891 http://rdf.ncbi.nlm.nih.gov/pubchem/disease/DZID7957 http://rdf.ncbi.nlm.nih.gov/pubchem/gene/MD5_22bd705d62805ab9c1b41e4293e9911c

Incoming Links

Predicate	Subject
isDiscussedBy	http://rdf.ncbi.nlm.nih.gov/pubchem/gene/GID148738

Total number of triples: 50.