reference/18687390

http://rdf.ncbi.nlm.nih.gov/pubchem/reference/18687390

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publicationName	Nature Genetics
startingPage	1120
bibliographicCitation	Brems H, Chmara M, Sahbatou M, Denayer E, Taniguchi K, Kato R, Somers R, Messiaen L, De Schepper S, Fryns JP, Cools J, Marynen P, Thomas G, Yoshimura A, Legius E. Germline loss-of-function mutations in SPRED1 cause a neurofibromatosis 1-like phenotype. Nat Genet. 2007 Sep;39(9):1120–6. doi: 10.1038/ng2113. PMID: 17704776.
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date	2007-08-19-04:00^^<http://www.w3.org/2001/XMLSchema#date>
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language	English
source	https://scigraph.springernature.com/ https://www.crossref.org/ https://pubmed.ncbi.nlm.nih.gov/
title	Germline loss-of-function mutations in SPRED1 cause a neurofibromatosis 1–like phenotype
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Total number of triples: 52.