20220693

Source:http://linkedlifedata.com/resource/pubmed/id/20220693

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Predicate	Object
rdf:type	pubmed:Citation
lifeskim:mentions	umls-concept:C0002726, umls-concept:C0205474, umls-concept:C1527178
pubmed:issue	2
pubmed:dateCreated	2010-3-11
pubmed:abstractText	Amyloidosis is a heterogeneous group of diseases characterized by normally soluble proteins deposited extracellularly in an abnormally folded, insoluble fibrillar form. This can lead to organ impairment and premature death. This article discusses the pathogenesis, classification system and means of diagnosis of the amyloid diseases.
pubmed:language	eng
pubmed:journal	http://linkedlifedata.com/resource/pubmed/journal/101257109
pubmed:citationSubset	IM
pubmed:chemical	http://linkedlifedata.com/resource/pubmed/chemical/Amyloid, http://linkedlifedata.com/resource/pubmed/chemical/Immunoglobulin Light Chains
pubmed:status	MEDLINE
pubmed:month	Feb
pubmed:issn	1750-8460
pubmed:author	pubmed-author:GibbsSimon D JSD, pubmed-author:HawkinsPhilip NPN
pubmed:issnType	Print
pubmed:volume	71
pubmed:owner	NLM
pubmed:authorsComplete	Y
pubmed:pagination	70-5
pubmed:meshHeading	pubmed-meshheading:20220693-Amyloid, pubmed-meshheading:20220693-Amyloidosis, pubmed-meshheading:20220693-Humans, pubmed-meshheading:20220693-Immunoglobulin Light Chains, pubmed-meshheading:20220693-Immunohistochemistry, pubmed-meshheading:20220693-Mutation
pubmed:year	2010
pubmed:articleTitle	Biochemical basis of the amyloid diseases.
pubmed:affiliation	UCL Medical School, Royal Free Hospital Campus, London.
pubmed:publicationType	Journal Article