9915977

Source:http://linkedlifedata.com/resource/pubmed/id/9915977

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Predicate	Object
rdf:type	pubmed:Citation
lifeskim:mentions	umls-concept:C0008665, umls-concept:C0024779, umls-concept:C0079429, umls-concept:C1708726, umls-concept:C1842137, umls-concept:C1863659, umls-concept:C1863660, umls-concept:C1882932
pubmed:issue	1
pubmed:dateCreated	1999-3-10
pubmed:grant	http://linkedlifedata.com/resource/pubmed/grant/DC00026, http://linkedlifedata.com/resource/pubmed/grant/K08 DC 00112
pubmed:language	eng
pubmed:journal	http://linkedlifedata.com/resource/pubmed/journal/0370475
pubmed:citationSubset	IM
pubmed:status	MEDLINE
pubmed:month	Jan
pubmed:issn	0002-9297
pubmed:author	pubmed-author:AttaieAA, pubmed-author:CasteleinC MCM, pubmed-author:LalwaniA KAK, pubmed-author:LuxfordW MWM, pubmed-author:MhatreA NAN, pubmed-author:WilcoxE RER
pubmed:issnType	Print
pubmed:volume	64
pubmed:owner	NLM
pubmed:authorsComplete	Y
pubmed:pagination	318-23
pubmed:dateRevised	2008-11-20
pubmed:meshHeading	pubmed-meshheading:9915977-Chromosome Mapping, pubmed-meshheading:9915977-Chromosomes, Human, Pair 22, pubmed-meshheading:9915977-Cochlea, pubmed-meshheading:9915977-Cochlear Diseases, pubmed-meshheading:9915977-Deafness, pubmed-meshheading:9915977-Female, pubmed-meshheading:9915977-Humans, pubmed-meshheading:9915977-Lod Score, pubmed-meshheading:9915977-Male, pubmed-meshheading:9915977-Pedigree, pubmed-meshheading:9915977-Saccule and Utricle, pubmed-meshheading:9915977-Software
pubmed:year	1999
pubmed:articleTitle	A new locus for nonsyndromic hereditary hearing impairment, DFNA17, maps to chromosome 22 and represents a gene for cochleosaccular degeneration.
pubmed:publicationType	Letter, Research Support, U.S. Gov't, P.H.S., Research Support, Non-U.S. Gov't