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7666917
Source:
http://linkedlifedata.com/resource/pubmed/id/7666917
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58
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Statements in which the resource exists as a subject.
Predicate
Object
rdf:type
pubmed:Citation
lifeskim:mentions
umls-concept:C0017337
,
umls-concept:C0025202
,
umls-concept:C0026882
,
umls-concept:C0039082
,
umls-concept:C0241888
,
umls-concept:C0346647
,
umls-concept:C0525037
,
umls-concept:C0684224
,
umls-concept:C1705280
,
umls-concept:C1879313
pubmed:issue
15
pubmed:dateCreated
1995-10-12
pubmed:commentsCorrections
http://linkedlifedata.com/resource/pubmed/commentcorrection/7666917-8552158
,
http://linkedlifedata.com/resource/pubmed/commentcorrection/7666917-8552160
pubmed:language
eng
pubmed:journal
http://linkedlifedata.com/resource/pubmed/journal/0255562
pubmed:citationSubset
AIM
pubmed:chemical
http://linkedlifedata.com/resource/pubmed/chemical/DNA
pubmed:status
MEDLINE
pubmed:month
Oct
pubmed:issn
0028-4793
pubmed:author
pubmed-author:BartschDD
,
pubmed-author:GoodfellowP JPJ
,
pubmed-author:WhelanA JAJ
pubmed:issnType
Print
pubmed:day
12
pubmed:volume
333
pubmed:geneSymbol
CDKN2
pubmed:owner
NLM
pubmed:authorsComplete
Y
pubmed:pagination
975-7
pubmed:dateRevised
2006-11-15
pubmed:meshHeading
pubmed-meshheading:7666917-Adult
,
pubmed-meshheading:7666917-Aged
,
pubmed-meshheading:7666917-Base Sequence
,
pubmed-meshheading:7666917-Carcinoma, Squamous Cell
,
pubmed-meshheading:7666917-DNA
,
pubmed-meshheading:7666917-Female
,
pubmed-meshheading:7666917-Genes, Tumor Suppressor
,
pubmed-meshheading:7666917-Humans
,
pubmed-meshheading:7666917-Male
,
pubmed-meshheading:7666917-Melanoma
,
pubmed-meshheading:7666917-Middle Aged
,
pubmed-meshheading:7666917-Molecular Sequence Data
,
pubmed-meshheading:7666917-Mutation
,
pubmed-meshheading:7666917-Neoplastic Syndromes, Hereditary
,
pubmed-meshheading:7666917-Pancreatic Neoplasms
,
pubmed-meshheading:7666917-Pedigree
,
pubmed-meshheading:7666917-Sequence Analysis, DNA
,
pubmed-meshheading:7666917-Skin Neoplasms
,
pubmed-meshheading:7666917-Syndrome
pubmed:year
1995
pubmed:articleTitle
Brief report: a familial syndrome of pancreatic cancer and melanoma with a mutation in the CDKN2 tumor-suppressor gene.
pubmed:affiliation
Department of Medicine, Washington University School of Medicine, St. Louis, USA.
pubmed:publicationType
Journal Article
,
Case Reports
,
Research Support, Non-U.S. Gov't