abnormal object recognition memory_Npc1<m1N>/Npc1<m1N>

http://metadb.riken.jp/0001458IBALBcC3HHeJC57BL6JNpc1m1NNpc1m1NNpc1m1N

abnormal object recognition memory_Npc1<m1N>/Npc1<m1N>

表現型アノテーション

MGI marker

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

• Niemann-Pick type C1
  http://metadb.riken.jp/db/mgi_rdf/MGI:1097712

遺伝子型

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

• Npc1<m1N>/Npc1<m1N>

アレルシンボル

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

• Npc1<m1N>

遺伝的背景

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

• involves: BALB/c * C3H/HeJ * C57BL/6J

MP annotation

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

• abnormal object recognition memory
  http://purl.obolibrary.org/obo/MP_0001458

文献

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

• Mahua. Maulik, et.al., Mutant human APP exacerbates pathology in a mouse model of NPC and its reversal by a β-cyclodextrin., Human molecular genetics, 2012, 21
  http://rdf.ncbi.nlm.nih.gov/pubmed/22869680