RDF of MGI data
表現型アノテーション
increased tumor incidence_Cdkn1a<tm1Led>/Cdkn1a<tm1Led>,Wrn<tm1Led>/Wrn<tm1Led>
http://metadb.riken.jp/0002020EI129S6SvEvTacorI129S6SvEvTacNIHBlackSwissCdkn1atm1LedCdkn1atm1LedWrntm1LedWrntm1LedWrntm1LedCdkn1atm1Led
increased tumor incidence_Cdkn1a<tm1Led>/Cdkn1a<tm1Led>,Wrn<tm1Led>/Wrn<tm1Led>(表現型アノテーション)
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increased tumor incidence_Cdkn1a<tm1Led>/Cdkn1a<tm1Led>,Wrn<tm1Led>/Wrn<tm1Led>
表現型アノテーション
MGI marker
http://metadb.riken.jp/db/mgi_rdf/variant_of
cyclin-dependent kinase inhibitor 1A (P21)
http://metadb.riken.jp/db/mgi_rdf/MGI:104556
Werner syndrome RecQ like helicase
http://metadb.riken.jp/db/mgi_rdf/MGI:109635
遺伝子型
http://metadb.riken.jp/db/mgi_rdf/allele_composition
Cdkn1a<tm1Led>/Cdkn1a<tm1Led>,Wrn<tm1Led>/Wrn<tm1Led>
アレルシンボル
http://metadb.riken.jp/db/mgi_rdf/allele_symbol
Wrn<tm1Led>|Cdkn1a<tm1Led>
遺伝的背景
http://metadb.riken.jp/db/mgi_rdf/genetic_background
either: (involves: 129S6/SvEvTac) or (involves: 129S6/SvEvTac * NIH Black Swiss)
MP annotation
http://metadb.riken.jp/db/bioresource_schema/brs_indicatesPhenotype
increased tumor incidence
http://purl.obolibrary.org/obo/MP_0002020
文献
http://purl.org/net/cito/citesAsAuthority
M. Lebel, et.al., Tumorigenic effect of nonfunctional p53 or p21 in mice mutant in the Werner syndrome helicase., Cancer research, 2001, 61
http://rdf.ncbi.nlm.nih.gov/pubmed/11280729
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