reference/11517735

http://rdf.ncbi.nlm.nih.gov/pubchem/reference/11517735

Outgoing Links

Predicate	Object
contentType	Journal Article\|Research Support, N.I.H., Intramural\|Research Support, Non-U.S. Gov't
endingPage	2005
issn	1945-7197 0021-972X
issueIdentifier	6
pageRange	1983-2005
publicationName	The Journal of clinical endocrinology and metabolism
startingPage	1983
hasFundingAgency	http://rdf.ncbi.nlm.nih.gov/pubchem/organization/MD5_bbe1ab52cb3b85124386d12499e4bc70 http://rdf.ncbi.nlm.nih.gov/pubchem/organization/MD5_eb4f340a1767b2ff28113b9d3c67834b
bibliographicCitation	Chasseloup F, Pankratz N, Lane J, Faucz FR, Keil MF, Chittiboina P, Kay DM, Hussein Tayeb T, Stratakis CA, Mills JL, Hernández-Ramírez LC. Germline CDKN1B Loss-of-Function Variants Cause Pediatric Cushing's Disease With or Without an MEN4 Phenotype. J Clin Endocrinol Metab. 2020 Jun 01;105(6). PMID: 32232325; PMCID: PMC7190031.
creator	http://rdf.ncbi.nlm.nih.gov/pubchem/author/ORCID_0000-0002-6599-6406 http://rdf.ncbi.nlm.nih.gov/pubchem/author/ORCID_0000-0003-4496-332X http://rdf.ncbi.nlm.nih.gov/pubchem/author/ORCID_0000-0002-9928-2698 http://rdf.ncbi.nlm.nih.gov/pubchem/author/ORCID_0000-0002-2228-9437 http://rdf.ncbi.nlm.nih.gov/pubchem/author/ORCID_0000-0001-9349-4756 http://rdf.ncbi.nlm.nih.gov/pubchem/author/MD5_6844c222f95f8493c35adee6ed995ec5 http://rdf.ncbi.nlm.nih.gov/pubchem/author/ORCID_0000-0001-5958-693X http://rdf.ncbi.nlm.nih.gov/pubchem/author/ORCID_0000-0001-5077-2218 http://rdf.ncbi.nlm.nih.gov/pubchem/author/ORCID_0000-0001-7959-9842 http://rdf.ncbi.nlm.nih.gov/pubchem/author/MD5_5832fb9cb76bf5a1308e7c2c31950c75 http://rdf.ncbi.nlm.nih.gov/pubchem/author/ORCID_0000-0002-4058-5520
date	2020-03-31-04:00^^<http://www.w3.org/2001/XMLSchema#date>
identifier	https://pubmed.ncbi.nlm.nih.gov/32232325 https://pubmed.ncbi.nlm.nih.gov/PMC7190031 https://doi.org/10.1210/clinem/dgaa160
isPartOf	https://portal.issn.org/resource/ISSN/0021-972X http://rdf.ncbi.nlm.nih.gov/pubchem/journal/4624 https://portal.issn.org/resource/ISSN/1945-7197
language	English
source	https://www.crossref.org/ https://pubmed.ncbi.nlm.nih.gov/
title	Germline CDKN1B Loss-of-Function Variants Cause Pediatric Cushing’s Disease With or Without an MEN4 Phenotype
discusses	http://id.nlm.nih.gov/mesh/C567059 http://id.nlm.nih.gov/mesh/M0023752 http://id.nlm.nih.gov/mesh/M0203045 http://id.nlm.nih.gov/mesh/M0400855
hasPrimarySubjectTerm	http://id.nlm.nih.gov/mesh/D056915 http://id.nlm.nih.gov/mesh/D050760Q000235 http://id.nlm.nih.gov/mesh/D009377Q000150 http://id.nlm.nih.gov/mesh/D003480Q000209 http://id.nlm.nih.gov/mesh/D015415Q000032 http://id.nlm.nih.gov/mesh/D018095
hasSubjectTerm	http://id.nlm.nih.gov/mesh/D009377Q000235 http://id.nlm.nih.gov/mesh/D006801 http://id.nlm.nih.gov/mesh/D005500 http://id.nlm.nih.gov/mesh/D010641 http://id.nlm.nih.gov/mesh/D005260 http://id.nlm.nih.gov/mesh/D003480Q000473 http://id.nlm.nih.gov/mesh/D055815 http://id.nlm.nih.gov/mesh/D000328 http://id.nlm.nih.gov/mesh/D011379 http://id.nlm.nih.gov/mesh/D008297 http://id.nlm.nih.gov/mesh/D002648 http://id.nlm.nih.gov/mesh/D009377Q000473 http://id.nlm.nih.gov/mesh/D000293
discussesAsDerivedByTextMining	http://rdf.ncbi.nlm.nih.gov/pubchem/disease/DZID8607 http://rdf.ncbi.nlm.nih.gov/pubchem/disease/DZID8615 http://rdf.ncbi.nlm.nih.gov/pubchem/disease/DZID10737 http://rdf.ncbi.nlm.nih.gov/pubchem/disease/DZID10859 http://rdf.ncbi.nlm.nih.gov/pubchem/gene/MD5_2c7bb8c933bedf612fa484b24eb8abd1 http://rdf.ncbi.nlm.nih.gov/pubchem/disease/DZID10250 http://rdf.ncbi.nlm.nih.gov/pubchem/disease/DZID7306

Incoming Links

Predicate	Subject
isDiscussedBy	http://rdf.ncbi.nlm.nih.gov/pubchem/gene/GID1027

Total number of triples: 64.