abnormal blood coagulation_F2<tm1Sjd>/F2<tm1Sjd>

http://metadb.riken.jp/0002551I129P2OlaHsdBlackSwissF2tm1SjdF2tm1SjdF2tm1Sjd

abnormal blood coagulation_F2<tm1Sjd>/F2<tm1Sjd>

表現型アノテーション

MGI marker

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

• coagulation factor II
  http://metadb.riken.jp/db/mgi_rdf/MGI:88380

遺伝子型

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

• F2<tm1Sjd>/F2<tm1Sjd>

アレルシンボル

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

• F2<tm1Sjd>

遺伝的背景

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

• involves: 129P2/OlaHsd * Black Swiss

MP annotation

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

• abnormal blood coagulation
  http://purl.obolibrary.org/obo/MP_0002551

文献

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

• W Y. Sun, et.al., Prothrombin deficiency results in embryonic and neonatal lethality in mice., Proceedings of the National Academy of Sciences of the United States of America, 1998, 95
  http://rdf.ncbi.nlm.nih.gov/pubmed/9636195