http://rdf.ncbi.nlm.nih.gov/pubchem/reference/2401839

Outgoing Links

Predicate Object
contentType Journal Article|Research Support, N.I.H., Extramural|Research Support, Non-U.S. Gov't
endingPage 335
issn 1552-4833
1552-4825
issueIdentifier 3
pageRange 328-335
publicationName American journal of medical genetics. Part A
startingPage 328
hasFundingAgency http://rdf.ncbi.nlm.nih.gov/pubchem/organization/MD5_e423e98d115894f5b30465dcb1113e0c
isSupportedBy http://rdf.ncbi.nlm.nih.gov/pubchem/grant/MD5_fb91256438345eae239c3b9d9a9b8e92
http://rdf.ncbi.nlm.nih.gov/pubchem/grant/MD5_fbabaf1bac00e1d0d9b4dbf76ba8507d
http://rdf.ncbi.nlm.nih.gov/pubchem/grant/MD5_4313d85bcdc356f9cfe640080c5841aa
bibliographicCitation Becerra‐Solano LE, Butler J, Castañeda‐Cisneros G, McCloskey DE, Wang X, Pegg AE, Schwartz CE, Sánchez‐Corona J, García‐Ortiz JE. A missense mutation, p.V132G, in the X‐linked spermine synthase gene (SMS) causes Snyder–Robinson syndrome. American J of Med Genetics Pt A. 2009 Feb 10;149A(3):328–35. doi: 10.1002/ajmg.a.32641.
creator http://rdf.ncbi.nlm.nih.gov/pubchem/author/MD5_dc62419f1146b128813904c7c71bb43c
http://rdf.ncbi.nlm.nih.gov/pubchem/author/MD5_0b746c29a0d2a724e0242deb18fdac5b
http://rdf.ncbi.nlm.nih.gov/pubchem/author/MD5_af3cb2224950a5b92c736c290600f977
http://rdf.ncbi.nlm.nih.gov/pubchem/author/MD5_586848b73718961183129f96f6a32d80
http://rdf.ncbi.nlm.nih.gov/pubchem/author/MD5_8edfc7e1a7d4ba98a4af777d98ea1dbd
http://rdf.ncbi.nlm.nih.gov/pubchem/author/MD5_1a3c76078d4fb7af5984a2243836bf2a
http://rdf.ncbi.nlm.nih.gov/pubchem/author/MD5_37b5b69c93bc7e9e7226d4317b9d53a8
http://rdf.ncbi.nlm.nih.gov/pubchem/author/MD5_697f7fe4a69e8d1936ccba2930802c54
http://rdf.ncbi.nlm.nih.gov/pubchem/author/MD5_1c2feb7420f0d9741befc804c2106bff
date 2009-02-10-04:00^^<http://www.w3.org/2001/XMLSchema#date>
identifier https://pubmed.ncbi.nlm.nih.gov/PMC2653108
https://doi.org/10.1002/ajmg.a.32641
https://pubmed.ncbi.nlm.nih.gov/19206178
isPartOf http://rdf.ncbi.nlm.nih.gov/pubchem/journal/32200
https://portal.issn.org/resource/ISSN/1552-4833
https://portal.issn.org/resource/ISSN/1552-4825
language English
source https://pubmed.ncbi.nlm.nih.gov/
https://www.crossref.org/
title A missense mutation, p.V132G, in the X‐linked spermine synthase gene (SMS) causes Snyder–Robinson syndrome
discusses http://id.nlm.nih.gov/mesh/M0020289
hasPrimarySubjectTerm http://id.nlm.nih.gov/mesh/D041321
http://id.nlm.nih.gov/mesh/D038901Q000235
http://id.nlm.nih.gov/mesh/D020125
http://id.nlm.nih.gov/mesh/D013097Q000235
http://id.nlm.nih.gov/mesh/D050172
hasSubjectTerm http://id.nlm.nih.gov/mesh/D035781
http://id.nlm.nih.gov/mesh/D008040
http://id.nlm.nih.gov/mesh/D008382Q000235
http://id.nlm.nih.gov/mesh/D055815
http://id.nlm.nih.gov/mesh/D010375
http://id.nlm.nih.gov/mesh/D004252
http://id.nlm.nih.gov/mesh/D006801
http://id.nlm.nih.gov/mesh/D005091
http://id.nlm.nih.gov/mesh/D008297
http://id.nlm.nih.gov/mesh/D012600Q000235
http://id.nlm.nih.gov/mesh/D000328
http://id.nlm.nih.gov/mesh/D008607Q000235
http://id.nlm.nih.gov/mesh/D010024Q000235
discussesAsDerivedByTextMining http://rdf.ncbi.nlm.nih.gov/pubchem/gene/MD5_18b43c6a536a8fe1362f7a3887936be6
http://rdf.ncbi.nlm.nih.gov/pubchem/disease/DZID1343
http://rdf.ncbi.nlm.nih.gov/pubchem/gene/MD5_0936f7fc2adf03a5b69319a7150086cd
http://rdf.ncbi.nlm.nih.gov/pubchem/disease/DZID8474
http://rdf.ncbi.nlm.nih.gov/pubchem/disease/DZID8738
http://rdf.ncbi.nlm.nih.gov/pubchem/gene/MD5_a2edb51617a3593f38ce1a6a755bec4e
http://rdf.ncbi.nlm.nih.gov/pubchem/gene/MD5_2995a6fdb6776aa7a783d6f332892f3d
http://rdf.ncbi.nlm.nih.gov/pubchem/disease/DZID10737
http://rdf.ncbi.nlm.nih.gov/pubchem/disease/DZID7679
http://rdf.ncbi.nlm.nih.gov/pubchem/disease/DZID10774

Incoming Links

Predicate Subject
isDiscussedBy http://rdf.ncbi.nlm.nih.gov/pubchem/protein/ACCP52788
http://rdf.ncbi.nlm.nih.gov/pubchem/gene/GID6611

Total number of triples: 64.