reference/18275578

http://rdf.ncbi.nlm.nih.gov/pubchem/reference/18275578

Outgoing Links

Predicate	Object
contentType	Journal Article\|Research Support, Non-U.S. Gov't
endingPage	98
issn	1744-5094 1381-6810
issueIdentifier	2
pageRange	91-98
publicationName	Ophthalmic Genetics
startingPage	91
hasFundingAgency	http://rdf.ncbi.nlm.nih.gov/pubchem/organization/MD5_78a6270e65565d04af89c389d1c0fad0
bibliographicCitation	Romero PT, Donoso R, López P, Miranda A, Rodríguez L, Chrzanowsky D, Asenjo MS, Burgos G, Villegas P, Desir J, Moya G, Herrera LM. Clinical features and possible founder mutation of the 8bp duplication mutation in the SLC4A11 gene causing corneal dystrophy and perceptive deafness in three South American families. Ophthalmic Genet. 2019 Apr;40(2):91–8. doi: 10.1080/13816810.2019.1571615. PMID: 30856043.
creator	http://rdf.ncbi.nlm.nih.gov/pubchem/author/MD5_04f551db6214363710fbb7fda14f13f9 http://rdf.ncbi.nlm.nih.gov/pubchem/author/MD5_7740ab0777a6f6c90080f1ef2c2a9f6f http://rdf.ncbi.nlm.nih.gov/pubchem/author/MD5_c21043ecb663255beba748b4e3b497e6 http://rdf.ncbi.nlm.nih.gov/pubchem/author/MD5_eb0de9c06d1d56919decf8b4b9ca68c8 http://rdf.ncbi.nlm.nih.gov/pubchem/author/MD5_aed44f13520a270d8ed484878b18446f http://rdf.ncbi.nlm.nih.gov/pubchem/author/MD5_a34e90a788f0dd921220934d0f3ed0a4 http://rdf.ncbi.nlm.nih.gov/pubchem/author/MD5_eedbca18c54c59dfdc5cc047fd57b77d http://rdf.ncbi.nlm.nih.gov/pubchem/author/MD5_c02c305cb1ca90129b361e473ed398de http://rdf.ncbi.nlm.nih.gov/pubchem/author/MD5_1cf18babbac75477bf14dcecb95b24ae http://rdf.ncbi.nlm.nih.gov/pubchem/author/MD5_db57a6907858427b596e611269a74369 http://rdf.ncbi.nlm.nih.gov/pubchem/author/MD5_12aa6a487842e0d383f9c831718bd748 http://rdf.ncbi.nlm.nih.gov/pubchem/author/MD5_2ed2fa1061a45e634a0fdfb11fc35072
date	2019-03-04-04:00^^<http://www.w3.org/2001/XMLSchema#date>
identifier	https://doi.org/10.1080/13816810.2019.1571615 https://pubmed.ncbi.nlm.nih.gov/30856043
isPartOf	http://rdf.ncbi.nlm.nih.gov/pubchem/journal/8553 https://portal.issn.org/resource/ISSN/1381-6810 https://portal.issn.org/resource/ISSN/1744-5094
language	English
source	https://www.crossref.org/ https://pubmed.ncbi.nlm.nih.gov/
title	Clinical features and possible founder mutation of the 8bp duplication mutation in the SLC4A11 gene causing corneal dystrophy and perceptive deafness in three South American families
discusses	http://id.nlm.nih.gov/mesh/C535473 http://id.nlm.nih.gov/mesh/M0076807 http://id.nlm.nih.gov/mesh/M0387092 http://id.nlm.nih.gov/mesh/M0027075
hasPrimarySubjectTerm	http://id.nlm.nih.gov/mesh/D003317Q000175 http://id.nlm.nih.gov/mesh/D018703 http://id.nlm.nih.gov/mesh/D003317Q000235 http://id.nlm.nih.gov/mesh/D006319Q000235 http://id.nlm.nih.gov/mesh/D020641 http://id.nlm.nih.gov/mesh/D006319Q000175 http://id.nlm.nih.gov/mesh/D017920Q000235 http://id.nlm.nih.gov/mesh/D020440Q000235 http://id.nlm.nih.gov/mesh/D027321Q000235
hasSubjectTerm	http://id.nlm.nih.gov/mesh/D004252 http://id.nlm.nih.gov/mesh/D008297 http://id.nlm.nih.gov/mesh/D020029 http://id.nlm.nih.gov/mesh/D005260 http://id.nlm.nih.gov/mesh/D006720 http://id.nlm.nih.gov/mesh/D006579 http://id.nlm.nih.gov/mesh/D010375 http://id.nlm.nih.gov/mesh/D000368 http://id.nlm.nih.gov/mesh/D005091Q000235 http://id.nlm.nih.gov/mesh/D000293 http://id.nlm.nih.gov/mesh/D014792Q000502 http://id.nlm.nih.gov/mesh/D002648 http://id.nlm.nih.gov/mesh/D001299 http://id.nlm.nih.gov/mesh/D000328 http://id.nlm.nih.gov/mesh/D006239 http://id.nlm.nih.gov/mesh/D003241 http://id.nlm.nih.gov/mesh/D055815 http://id.nlm.nih.gov/mesh/D006801
discussesAsDerivedByTextMining	http://rdf.ncbi.nlm.nih.gov/pubchem/disease/DZID313 http://rdf.ncbi.nlm.nih.gov/pubchem/disease/DZID7915 http://rdf.ncbi.nlm.nih.gov/pubchem/disease/DZID8600 http://rdf.ncbi.nlm.nih.gov/pubchem/gene/MD5_be72108df5a3fd1e2c26c42686b63518 http://rdf.ncbi.nlm.nih.gov/pubchem/disease/DZID2491 http://rdf.ncbi.nlm.nih.gov/pubchem/compound/CID10085878 http://rdf.ncbi.nlm.nih.gov/pubchem/disease/DZID10757 http://rdf.ncbi.nlm.nih.gov/pubchem/disease/DZID7343

Incoming Links

Predicate	Subject
isDiscussedBy	http://rdf.ncbi.nlm.nih.gov/pubchem/gene/GID83959

Total number of triples: 72.