http://rdf.ncbi.nlm.nih.gov/pubchem/reference/14174604

Outgoing Links

Predicate Object
contentType Letter|Research Support, Non-U.S. Gov't
issn 1399-3003
0903-1936
issueIdentifier 1
pageRange 1601478-
publicationName The European respiratory journal
startingPage 1601478
hasFundingAgency http://rdf.ncbi.nlm.nih.gov/pubchem/organization/MD5_baa0c8a8d2342709333532192429b449
http://rdf.ncbi.nlm.nih.gov/pubchem/organization/MD5_d32a1417ff1a4e0a9b1785901415bad9
http://rdf.ncbi.nlm.nih.gov/pubchem/organization/MD5_70422ffc715a4e5643446f33fe9d367d
http://rdf.ncbi.nlm.nih.gov/pubchem/organization/MD5_5aefbc46505a27dc22642156e6759896
bibliographicCitation Becker KL, Arts P, Jaeger M, Plantinga TS, Gilissen C, van Laarhoven A, van Ingen J, Veltman JA, Joosten LAB, Hoischen A, Netea MG, Iseman MD, Chan ED, van de Veerdonk FL. MST1R mutation as a genetic cause of Lady Windermere syndrome. Eur Respir J. 2016 Dec 19;49(1):1601478. doi: 10.1183/13993003.01478-2016.
creator http://rdf.ncbi.nlm.nih.gov/pubchem/author/ORCID_0000-0001-6994-493X
http://rdf.ncbi.nlm.nih.gov/pubchem/author/MD5_f2170d4298f0ed4f287499314ea0a881
http://rdf.ncbi.nlm.nih.gov/pubchem/author/MD5_43299452b0adb558824270328790f83c
http://rdf.ncbi.nlm.nih.gov/pubchem/author/MD5_b6d5e1e4563b624bd13b45059f5ff7b7
http://rdf.ncbi.nlm.nih.gov/pubchem/author/MD5_74020b8822cce6d73a5155140efba85a
http://rdf.ncbi.nlm.nih.gov/pubchem/author/MD5_49c5cc131a7ac4a07a2631fa163287db
http://rdf.ncbi.nlm.nih.gov/pubchem/author/MD5_e00166b9d609dfc25d8041924fd34deb
http://rdf.ncbi.nlm.nih.gov/pubchem/author/ORCID_0000-0002-6742-6239
http://rdf.ncbi.nlm.nih.gov/pubchem/author/MD5_d57435332897889d917af04065f1dc30
http://rdf.ncbi.nlm.nih.gov/pubchem/author/MD5_888b870d228c4e659a1559a9e1d04de9
http://rdf.ncbi.nlm.nih.gov/pubchem/author/MD5_5dac89b91fce3628a4e21b81a53a3786
http://rdf.ncbi.nlm.nih.gov/pubchem/author/MD5_7ab53e8c310f9c995fa6de4477e40302
http://rdf.ncbi.nlm.nih.gov/pubchem/author/MD5_7399d19fc5646af281d379e99bd158a9
http://rdf.ncbi.nlm.nih.gov/pubchem/author/ORCID_0000-0003-1693-9699
http://rdf.ncbi.nlm.nih.gov/pubchem/author/ORCID_0000-0002-6607-4075
http://rdf.ncbi.nlm.nih.gov/pubchem/author/MD5_15ceb4fc2707a883447c278b19214c8a
http://rdf.ncbi.nlm.nih.gov/pubchem/author/MD5_3f5db4c39a93f1b52501b1282ba88ec0
http://rdf.ncbi.nlm.nih.gov/pubchem/author/MD5_8975f205faf0763cf266a8f0688721ee
date 2016-12-19-04:00^^<http://www.w3.org/2001/XMLSchema#date>
identifier https://pubmed.ncbi.nlm.nih.gov/28100548
https://doi.org/10.1183/13993003.01478-2016
isPartOf http://rdf.ncbi.nlm.nih.gov/pubchem/journal/3682
https://portal.issn.org/resource/ISSN/0903-1936
https://portal.issn.org/resource/ISSN/1399-3003
language English
source https://www.crossref.org/
https://pubmed.ncbi.nlm.nih.gov/
title MST1R mutation as a genetic cause of Lady Windermere syndrome
discusses http://id.nlm.nih.gov/mesh/M0011490
http://id.nlm.nih.gov/mesh/M0328256
http://id.nlm.nih.gov/mesh/M0215825
hasPrimarySubjectTerm http://id.nlm.nih.gov/mesh/D020794Q000235
http://id.nlm.nih.gov/mesh/D012600Q000235
http://id.nlm.nih.gov/mesh/D008945Q000235
http://id.nlm.nih.gov/mesh/D005660Q000235
http://id.nlm.nih.gov/mesh/D020022
http://id.nlm.nih.gov/mesh/D015269
hasSubjectTerm http://id.nlm.nih.gov/mesh/D010375
http://id.nlm.nih.gov/mesh/D020125
http://id.nlm.nih.gov/mesh/D005192
http://id.nlm.nih.gov/mesh/D005260
http://id.nlm.nih.gov/mesh/D007371Q000378
http://id.nlm.nih.gov/mesh/D001835
http://id.nlm.nih.gov/mesh/D009154
http://id.nlm.nih.gov/mesh/D015270Q000150
http://id.nlm.nih.gov/mesh/D005660Q000150
http://id.nlm.nih.gov/mesh/D013577
http://id.nlm.nih.gov/mesh/D006801
http://id.nlm.nih.gov/mesh/D008297
http://id.nlm.nih.gov/mesh/D012600Q000150
http://id.nlm.nih.gov/mesh/D008945Q000150
discussesAsDerivedByTextMining http://rdf.ncbi.nlm.nih.gov/pubchem/disease/DZID9688
http://rdf.ncbi.nlm.nih.gov/pubchem/gene/MD5_f52e7c4612339c86d96a13139558ca02

Incoming Links

Predicate Subject
isDiscussedBy http://rdf.ncbi.nlm.nih.gov/pubchem/gene/GID4486

Total number of triples: 66.