RDF of MGI data
表現型アノテーション
decreased vasoconstriction_Tg(Notch3*R169C)88Bbb/0
http://metadb.riken.jp/0003026IFVBNTgNotch3R169C88Bbb0TgNotch3R169C88Bbb
decreased vasoconstriction_Tg(Notch3*R169C)88Bbb/0(表現型アノテーション)
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decreased vasoconstriction_Tg(Notch3*R169C)88Bbb/0
表現型アノテーション
MGI marker
http://metadb.riken.jp/db/mgi_rdf/variant_of
transgene insertion 88, Norbert Hubner
http://metadb.riken.jp/db/mgi_rdf/MGI:4429554
遺伝子型
http://metadb.riken.jp/db/mgi_rdf/allele_composition
Tg(Notch3*R169C)88Bbb/0
アレルシンボル
http://metadb.riken.jp/db/mgi_rdf/allele_symbol
Tg(Notch3*R169C)88Bbb
遺伝的背景
http://metadb.riken.jp/db/mgi_rdf/genetic_background
involves: FVB/N
MP annotation
http://metadb.riken.jp/db/bioresource_schema/brs_indicatesPhenotype
decreased vasoconstriction
http://purl.obolibrary.org/obo/MP_0003026
文献
http://purl.org/net/cito/citesAsAuthority
Fabrice. Dabertrand, et.al., Potassium channelopathy-like defect underlies early-stage cerebrovascular dysfunction in a genetic model of small vessel disease., Proceedings of the National Academy of Sciences of the United States of America, 2015, 112
http://rdf.ncbi.nlm.nih.gov/pubmed/25646445
Anne. Joutel, et.al., Cerebrovascular dysfunction and microcirculation rarefaction precede white matter lesions in a mouse genetic model of cerebral ischemic small vessel disease., The Journal of clinical investigation, 2010, 120
http://rdf.ncbi.nlm.nih.gov/pubmed/20071773
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