20108420

Source:http://linkedlifedata.com/resource/pubmed/id/20108420

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Predicate	Object
rdf:type	pubmed:Citation
lifeskim:mentions	umls-concept:C0012634, umls-concept:C0026882, umls-concept:C0086418, umls-concept:C0205314, umls-concept:C0679622, umls-concept:C1426807, umls-concept:C1521733, umls-concept:C1706510, umls-concept:C1969623
pubmed:issue	1
pubmed:dateCreated	2010-1-27
pubmed:language	eng
pubmed:journal	http://linkedlifedata.com/resource/pubmed/journal/7613873
pubmed:citationSubset	IM
pubmed:chemical	http://linkedlifedata.com/resource/pubmed/chemical/Codon, http://linkedlifedata.com/resource/pubmed/chemical/Intracellular Signaling Peptides..., http://linkedlifedata.com/resource/pubmed/chemical/Membrane Proteins, http://linkedlifedata.com/resource/pubmed/chemical/SPRED1 protein, human
pubmed:status	MEDLINE
pubmed:month	Jan
pubmed:issn	1432-1203
pubmed:author	pubmed-author:JimHoi PingHP, pubmed-author:UpadhyayaMeenaM
pubmed:issnType	Electronic
pubmed:volume	127
pubmed:owner	NLM
pubmed:authorsComplete	Y
pubmed:pagination	111
pubmed:meshHeading	pubmed-meshheading:20108420-Base Sequence, pubmed-meshheading:20108420-Codon, pubmed-meshheading:20108420-Humans, pubmed-meshheading:20108420-Intracellular Signaling Peptides and Proteins, pubmed-meshheading:20108420-Membrane Proteins, pubmed-meshheading:20108420-Sequence Deletion, pubmed-meshheading:20108420-Syndrome
pubmed:year	2010
pubmed:articleTitle	Novel human pathological mutations. Gene symbol: SPRED1. Disease: Legius syndrome.
pubmed:affiliation	NF1 lab, Institute of Medical Genetics, University of Wales College of Medicine, CF14 4XN, Cardiff, United Kingdom. jimh@cardiff.ac.uk
pubmed:publicationType	Journal Article