paresis_Notch3<tm1.1Dwr>/Notch3<+>

http://metadb.riken.jp/0000754I129SSvEvSwissNotch3tm11DwrNotch3Notch3tm11DwrNotch3

paresis_Notch3<tm1.1Dwr>/Notch3<+>

表現型アノテーション

MGI marker

http://metadb.riken.jp/db/mgi_rdf/variant_of

• notch 3
  http://metadb.riken.jp/db/mgi_rdf/MGI:99460

遺伝子型

http://metadb.riken.jp/db/mgi_rdf/allele_composition

• Notch3<tm1.1Dwr>/Notch3<+>

アレルシンボル

http://metadb.riken.jp/db/mgi_rdf/allele_symbol

• Notch3<tm1.1Dwr>|Notch3<+>

遺伝的背景

http://metadb.riken.jp/db/mgi_rdf/genetic_background

• involves: 129S/SvEv * Swiss

MP annotation

http://metadb.riken.jp/db/bioresource_schema/brs_indicatesPhenotype

• paresis
  http://purl.obolibrary.org/obo/MP_0000754

文献

http://purl.org/net/cito/citesAsAuthority

• Goedele. Wallays, et.al., Notch3 Arg170Cys knock-in mice display pathologic and clinical features of the neurovascular disorder cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy., Arteriosclerosis, thrombosis, and vascular biology, 2011, 31
  http://rdf.ncbi.nlm.nih.gov/pubmed/21940951