abnormal choroid pigmentation in RBRC02886

http://metadb.riken.jp/db/rikenbrc_mouse/Phenotype_1021586

abnormal choroid pigmentation in RBRC02886

表現型アノテーション

表現型アノテーション

http://www.w3.org/2000/01/rdf-schema#label

• abnormal choroid pigmentation in RBRC02886

Mammalian Phenotype ontology

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

• abnormal choroid pigmentation
  http://purl.obolibrary.org/obo/MP_0005100

測定対象実体

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

測定対象形質（性質）

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

測定結果の値

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

• abnormal
  http://purl.obolibrary.org/obo/PATO_0000460

アノテーションタイプ

http://purl.obolibrary.org/obo/IAO_0000115

• MGIのアノテーションを採用（人がチェック）

マウス系統

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

• EOD/ThpNkc-Cno<cno-II>/Nkc
  http://metadb.riken.jp/db/rikenbrc_mouse/RBRC02886

測定対象個体

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

• [RBRC02886, EOD/ThpNkc-Cno<cno-II>/Nkc]

参考文献

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

• B. Gwynn, et.al., Defects in the cappuccino (cno) gene on mouse chromosome 5 and human 4p cause Hermansky-Pudlak syndrome by an AP-3-independent mechanism., Blood, 2000, 96
  http://rdf.ncbi.nlm.nih.gov/pubmed/11110696