exencephaly_Nog<tm1Amc>/Nog<tm1Amc>

http://metadb.riken.jp/0000914D1129S1Nogtm1AmcNogtm1AmcNogtm1AmcNogtm1Amc

exencephaly_Nog<tm1Amc>/Nog<tm1Amc>

表現型アノテーション

MGI marker

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

• noggin
  http://metadb.riken.jp/db/mgi_rdf/MGI:104327

遺伝子型

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

• Nog<tm1Amc>/Nog<tm1Amc>

アレルシンボル

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

• Nog<tm1Amc>

遺伝的背景

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

• D1.129S1-Nog<tm1Amc>

MP annotation

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

• exencephaly
  http://purl.obolibrary.org/obo/MP_0000914

文献

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

• Przemko. Tylzanowski, et.al., The Noggin null mouse phenotype is strain dependent and haploinsufficiency leads to skeletal defects., Developmental dynamics : an official publication of the American Association of Anatomists, 2006, 235
  http://rdf.ncbi.nlm.nih.gov/pubmed/16598734