abnormal retina morphology_Prnp<tm3Lnq>/Prnp<tm3Lnq>

http://metadb.riken.jp/0001325I129P2OlaHsdC57BL6NPrnptm3LnqPrnptm3LnqPrnptm3Lnq

abnormal retina morphology_Prnp<tm3Lnq>/Prnp<tm3Lnq>

表現型アノテーション

MGI marker

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

• prion protein
  http://metadb.riken.jp/db/mgi_rdf/MGI:97769

遺伝子型

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

• Prnp<tm3Lnq>/Prnp<tm3Lnq>

アレルシンボル

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

• Prnp<tm3Lnq>

遺伝的背景

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

• involves: 129P2/OlaHsd * C57BL/6N

MP annotation

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

• abnormal retina morphology
  http://purl.obolibrary.org/obo/MP_0001325

文献

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

• Walker S. Jackson, et.al., Profoundly different prion diseases in knock-in mice carrying single PrP codon substitutions associated with human diseases., Proceedings of the National Academy of Sciences of the United States of America, 2013, 110
  http://rdf.ncbi.nlm.nih.gov/pubmed/23959875