reference/26878708

http://rdf.ncbi.nlm.nih.gov/pubchem/reference/26878708

Outgoing Links

Predicate	Object
contentType	Journal Article\|Research Support, Non-U.S. Gov't
endingPage	9
issn	1128-2460
pageRange	82-9
publicationName	Acta myologica : myopathies and cardiomyopathies : official journal of the Mediterranean Society of Myology
startingPage	82
bibliographicCitation	Rinaldi F, Botta A, Vallo L, Contino G, Morgante A, Iraci R, Catalli C, Silvestri G, Ventriglia VM, Politano L, Novelli G. Analysis of Single Nucleotide Polymorphisms (SNPs) of the small-conductance calcium activated potassium channel (SK3) gene as genetic modifier of the cardiac phenotype in myotonic dystrophy type 1 patients. Acta Myol. 2008 Dec;27():82–9. PMID: 19472917; PMCID: PMC2858941.
creator	http://rdf.ncbi.nlm.nih.gov/pubchem/author/MD5_0e15e897a63dc06722995ba9ef0ed458 http://rdf.ncbi.nlm.nih.gov/pubchem/author/MD5_d3b3e19728288da3d7258d6abb6eea30 http://rdf.ncbi.nlm.nih.gov/pubchem/author/MD5_ef302b9ddb307d4733ab7f763defa5e3 http://rdf.ncbi.nlm.nih.gov/pubchem/author/MD5_44bcfdc702083acdce22c9dc2bce009c http://rdf.ncbi.nlm.nih.gov/pubchem/author/MD5_5d191e1cb86e95a8885d8d06a3066609 http://rdf.ncbi.nlm.nih.gov/pubchem/author/MD5_76ab3517c22cb5908ca69dee34451ee8 http://rdf.ncbi.nlm.nih.gov/pubchem/author/MD5_70b74b04c8a628005f07a07db96007bb http://rdf.ncbi.nlm.nih.gov/pubchem/author/MD5_b41f2fd81d008a417f08d9c4671f5e60 http://rdf.ncbi.nlm.nih.gov/pubchem/author/MD5_a1a4745a04e7bb60ace1ad22a4355821 http://rdf.ncbi.nlm.nih.gov/pubchem/author/MD5_3f32d8ff506ff1f4396eab590ab9f189 http://rdf.ncbi.nlm.nih.gov/pubchem/author/MD5_563d76348781d88d2b2b57f8bdb5b45e
date	200812
identifier	https://pubmed.ncbi.nlm.nih.gov/19472917 https://pubmed.ncbi.nlm.nih.gov/PMC2858941
isPartOf	http://rdf.ncbi.nlm.nih.gov/pubchem/journal/30238 https://portal.issn.org/resource/ISSN/1128-2460
language	English
source	https://pubmed.ncbi.nlm.nih.gov/
title	Analysis of Single Nucleotide Polymorphisms (SNPs) of the small-conductance calcium activated potassium channel (SK3) gene as genetic modifier of the cardiac phenotype in myotonic dystrophy type 1 patients
discusses	http://id.nlm.nih.gov/mesh/M0265387 http://id.nlm.nih.gov/mesh/M0019167 http://id.nlm.nih.gov/mesh/M0360419
hasPrimarySubjectTerm	http://id.nlm.nih.gov/mesh/D009223Q000235 http://id.nlm.nih.gov/mesh/D020641Q000235 http://id.nlm.nih.gov/mesh/D054537Q000235 http://id.nlm.nih.gov/mesh/D010641 http://id.nlm.nih.gov/mesh/D051640Q000235
hasSubjectTerm	http://id.nlm.nih.gov/mesh/D008297 http://id.nlm.nih.gov/mesh/D001706 http://id.nlm.nih.gov/mesh/D005260 http://id.nlm.nih.gov/mesh/D054537Q000453 http://id.nlm.nih.gov/mesh/D006801 http://id.nlm.nih.gov/mesh/D016022 http://id.nlm.nih.gov/mesh/D012307 http://id.nlm.nih.gov/mesh/D051640Q000378 http://id.nlm.nih.gov/mesh/D015331 http://id.nlm.nih.gov/mesh/D020022Q000235 http://id.nlm.nih.gov/mesh/D018482Q000473 http://id.nlm.nih.gov/mesh/D005787Q000235 http://id.nlm.nih.gov/mesh/D005838 http://id.nlm.nih.gov/mesh/D000328 http://id.nlm.nih.gov/mesh/D012333Q000378 http://id.nlm.nih.gov/mesh/D009223Q000378 http://id.nlm.nih.gov/mesh/D008875 http://id.nlm.nih.gov/mesh/D009223Q000473
discussesAsDerivedByTextMining	http://rdf.ncbi.nlm.nih.gov/pubchem/disease/DZID8655 http://rdf.ncbi.nlm.nih.gov/pubchem/disease/DZID8576 http://rdf.ncbi.nlm.nih.gov/pubchem/disease/DZID7918 http://rdf.ncbi.nlm.nih.gov/pubchem/gene/MD5_9979d0cda3f2b587c3dda57ad8944544 http://rdf.ncbi.nlm.nih.gov/pubchem/gene/MD5_db3ddc66a571bb8860a2c188de2aa7f3

Incoming Links

Predicate	Subject
isDiscussedBy	http://rdf.ncbi.nlm.nih.gov/pubchem/gene/GID3782

Total number of triples: 58.