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19693995
Source:
http://linkedlifedata.com/resource/pubmed/id/19693995
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Statements in which the resource exists as a subject.
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:C1413586
,
umls-concept:C1521733
,
umls-concept:C1567741
,
umls-concept:C1706510
pubmed:issue
2
pubmed:dateCreated
2009-8-19
pubmed:databankReference
http://linkedlifedata.com/resource/pubmed/xref/GENBANK/HD080028
pubmed:language
eng
pubmed:journal
http://linkedlifedata.com/resource/pubmed/journal/7613873
pubmed:citationSubset
IM
pubmed:chemical
http://linkedlifedata.com/resource/pubmed/chemical/COL4A5 protein, human
,
http://linkedlifedata.com/resource/pubmed/chemical/Codon
,
http://linkedlifedata.com/resource/pubmed/chemical/Collagen Type IV
,
http://linkedlifedata.com/resource/pubmed/chemical/Nucleotides
pubmed:status
MEDLINE
pubmed:month
Aug
pubmed:issn
1432-1203
pubmed:author
pubmed-author:EllisonJayJ
pubmed:issnType
Electronic
pubmed:volume
126
pubmed:owner
NLM
pubmed:authorsComplete
Y
pubmed:pagination
331
pubmed:meshHeading
pubmed-meshheading:19693995-Base Sequence
,
pubmed-meshheading:19693995-Codon
,
pubmed-meshheading:19693995-Collagen Type IV
,
pubmed-meshheading:19693995-Female
,
pubmed-meshheading:19693995-Gene Deletion
,
pubmed-meshheading:19693995-Hematuria
,
pubmed-meshheading:19693995-Humans
,
pubmed-meshheading:19693995-Molecular Sequence Data
,
pubmed-meshheading:19693995-Nephritis, Hereditary
,
pubmed-meshheading:19693995-Nucleotides
,
pubmed-meshheading:19693995-Proteinuria
,
pubmed-meshheading:19693995-Sequence Analysis, DNA
pubmed:year
2009
pubmed:articleTitle
Novel human pathological mutations. Gene symbol: COL4A5. Disease: Alport syndrome.
pubmed:affiliation
Medical Genetics, Mayo Clinic, Rochester, 55905, USA. ellison.jay@mayo.edu
pubmed:publicationType
Journal Article