http://rdf.ncbi.nlm.nih.gov/pubchem/reference/33022358

Outgoing Links

Predicate Object
contentType Case Reports|Journal Article|Research Support, Non-U.S. Gov't
endingPage 195
issn 0307-6938
issueIdentifier 2
pageRange 190-195
publicationName Clinical and Experimental Dermatology
startingPage 190
hasFundingAgency http://rdf.ncbi.nlm.nih.gov/pubchem/organization/MD5_faa396198b8c353291efe783e7e5205d
http://rdf.ncbi.nlm.nih.gov/pubchem/organization/MD5_bc8f98b2dce7dbd4ffdf72720dd96738
http://rdf.ncbi.nlm.nih.gov/pubchem/organization/MD5_594fa5325f2e5d4fa5a5374c8ac0a0ef
http://rdf.ncbi.nlm.nih.gov/pubchem/organization/MD5_c84a83e8991a1611281c65cb0102cf01
http://rdf.ncbi.nlm.nih.gov/pubchem/organization/MD5_9a18968af130ca0040b68b9e2eec4838
http://rdf.ncbi.nlm.nih.gov/pubchem/organization/MD5_96b7670af5f2dc86914c285862cc23b4
bibliographicCitation Sulák A, Tóth L, Farkas K, Tripolszki K, Fábos B, Kemény L, Vályi P, Nagy K, Nagy N, Széll M. One mutation, two phenotypes: a single nonsense mutation of the CTSC gene causes two clinically distinct phenotypes. Clin Exp Dermatol. 2016 Mar;41(2):190–5. doi: 10.1111/ced.12710. PMID: 26205983.
creator http://rdf.ncbi.nlm.nih.gov/pubchem/author/MD5_d294eedfcac99135ff52b03a8ebc1301
http://rdf.ncbi.nlm.nih.gov/pubchem/author/MD5_87e15873724bdfff1d29e4bf4ede85c1
http://rdf.ncbi.nlm.nih.gov/pubchem/author/MD5_d65f1ed20993b92f66828ec4e4ef2a4c
http://rdf.ncbi.nlm.nih.gov/pubchem/author/MD5_c90fd19326a94affb340c6d13fab24d8
http://rdf.ncbi.nlm.nih.gov/pubchem/author/MD5_a44bb6fbdf0150dd53db3f1a5dfc2df6
http://rdf.ncbi.nlm.nih.gov/pubchem/author/MD5_0dec6b340085a451341d44b7b92232e5
http://rdf.ncbi.nlm.nih.gov/pubchem/author/MD5_a80d0372830873c0ba713f36add45703
http://rdf.ncbi.nlm.nih.gov/pubchem/author/MD5_e962f0430280b8daac20fdd72aa3344b
http://rdf.ncbi.nlm.nih.gov/pubchem/author/MD5_854c40321e690cc1cfafdd26eb44a932
http://rdf.ncbi.nlm.nih.gov/pubchem/author/MD5_8da928c5a6224a2d16c7434bb46b6078
date 2015-07-24-04:00^^<http://www.w3.org/2001/XMLSchema#date>
identifier https://doi.org/10.1111/ced.12710
https://pubmed.ncbi.nlm.nih.gov/26205983
isPartOf http://rdf.ncbi.nlm.nih.gov/pubchem/journal/3011
https://portal.issn.org/resource/ISSN/0307-6938
language English
source https://www.crossref.org/
https://pubmed.ncbi.nlm.nih.gov/
title One mutation, two phenotypes: a single nonsense mutation of theCTSCgene causes two clinically distinct phenotypes
discusses http://id.nlm.nih.gov/mesh/C537627
http://id.nlm.nih.gov/mesh/M0262814
http://id.nlm.nih.gov/mesh/M0027616
hasPrimarySubjectTerm http://id.nlm.nih.gov/mesh/D010214Q000235
http://id.nlm.nih.gov/mesh/D018389
http://id.nlm.nih.gov/mesh/D020789Q000235
http://id.nlm.nih.gov/mesh/D030981Q000235
hasSubjectTerm http://id.nlm.nih.gov/mesh/D005260
http://id.nlm.nih.gov/mesh/D005838
http://id.nlm.nih.gov/mesh/D006801
http://id.nlm.nih.gov/mesh/D000328
http://id.nlm.nih.gov/mesh/D010641
http://id.nlm.nih.gov/mesh/D008297
discussesAsDerivedByTextMining http://rdf.ncbi.nlm.nih.gov/pubchem/gene/MD5_1f1aead17c6279e8f206ea12c5ded8fb
http://rdf.ncbi.nlm.nih.gov/pubchem/disease/DZID2147
http://rdf.ncbi.nlm.nih.gov/pubchem/protein/EC_3.4.14.1

Incoming Links

Predicate Subject
isDiscussedBy http://rdf.ncbi.nlm.nih.gov/pubchem/gene/GID1075

Total number of triples: 50.