reference/1040349

http://rdf.ncbi.nlm.nih.gov/pubchem/reference/1040349

Outgoing Links

Predicate	Object
contentType	Journal Article
endingPage	459
issn	0009-9163 1399-0004
issueIdentifier	5
pageRange	454-459
publicationName	Clinical Genetics
startingPage	454
bibliographicCitation	Auber B, Burfeind P, Herold S, Schoner K, Simson G, Rauskolb R, Rehder H. A disease causing deletion of 29 base pairs in intron 15 in the MKS1 gene is highly associated with the campomelic variant of the Meckel–Gruber syndrome. Clinical Genetics. 2007 Sep 10;72(5):454–9. doi: 10.1111/j.1399-0004.2007.00880.x.
creator	http://rdf.ncbi.nlm.nih.gov/pubchem/author/MD5_48500991dc6960032059f00a808f71e3 http://rdf.ncbi.nlm.nih.gov/pubchem/author/MD5_aa7487d2b8d88865047c5a59770e59f3 http://rdf.ncbi.nlm.nih.gov/pubchem/author/MD5_f2937f435db35ff2536058b9c0514d8f http://rdf.ncbi.nlm.nih.gov/pubchem/author/MD5_a8219fd25a00fc26b116f09a752cb857 http://rdf.ncbi.nlm.nih.gov/pubchem/author/MD5_21c618b0c492337bce3f6900fd61c0ce http://rdf.ncbi.nlm.nih.gov/pubchem/author/MD5_9b791919d932d572ed06c68e6bf3b835 http://rdf.ncbi.nlm.nih.gov/pubchem/author/MD5_1e9f982adec6a7a1ac95b8a6bc419d14
date	2007-09-10-04:00^^<http://www.w3.org/2001/XMLSchema#date>
identifier	https://pubmed.ncbi.nlm.nih.gov/17935508 https://doi.org/10.1111/j.1399-0004.2007.00880.x
isPartOf	http://rdf.ncbi.nlm.nih.gov/pubchem/journal/3010 https://portal.issn.org/resource/ISSN/1399-0004 https://portal.issn.org/resource/ISSN/0009-9163
language	English
source	https://pubmed.ncbi.nlm.nih.gov/ https://www.crossref.org/
title	A disease causing deletion of 29 base pairs in intron 15 in the MKS1 gene is highly associated with the campomelic variant of the Meckel–Gruber syndrome
discusses	http://id.nlm.nih.gov/mesh/M0496604 http://id.nlm.nih.gov/mesh/M0017890
hasPrimarySubjectTerm	http://id.nlm.nih.gov/mesh/D007438 http://id.nlm.nih.gov/mesh/D017689Q000235 http://id.nlm.nih.gov/mesh/D011506Q000235 http://id.nlm.nih.gov/mesh/D002490Q000002 http://id.nlm.nih.gov/mesh/D017384 http://id.nlm.nih.gov/mesh/D000015Q000235
hasSubjectTerm	http://id.nlm.nih.gov/mesh/D008297 http://id.nlm.nih.gov/mesh/D011859 http://id.nlm.nih.gov/mesh/D005787 http://id.nlm.nih.gov/mesh/D006801 http://id.nlm.nih.gov/mesh/D001483 http://id.nlm.nih.gov/mesh/D008969 http://id.nlm.nih.gov/mesh/D004252 http://id.nlm.nih.gov/mesh/D013577 http://id.nlm.nih.gov/mesh/D037881Q000000981 http://id.nlm.nih.gov/mesh/D005820 http://id.nlm.nih.gov/mesh/D005260
discussesAsDerivedByTextMining	http://rdf.ncbi.nlm.nih.gov/pubchem/gene/MD5_c9811ae673f9fbd3667bace223447ee1 http://rdf.ncbi.nlm.nih.gov/pubchem/disease/DZID879 http://rdf.ncbi.nlm.nih.gov/pubchem/disease/DZID10737

Incoming Links

Predicate	Subject
isDiscussedBy	http://rdf.ncbi.nlm.nih.gov/pubchem/gene/GID287612 http://rdf.ncbi.nlm.nih.gov/pubchem/gene/GID54903

Total number of triples: 50.