Cell Line Ontology (Chinese Translation)

Last uploaded: November 21, 2019

Preferred Name	简单遗传疾病
Definitions	“遗传性疾病是一种或多种异常等位基因的结果，可能是显性的（异常等位基因的单一拷贝足以引起疾病），半显性或隐性的（需要基因的两个拷贝有异常的等位基因）“。 [DO：WK，LS]
ID	http://purl.obolibrary.org/obo/DOID_0050177
comment	“遗传性疾病是一种或多种异常等位基因的结果，可能是显性的（异常等位基因的单一拷贝足以引起疾病），半显性或隐性的（需要基因的两个拷贝有异常的等位基因）“。 [DO：WK，LS]
prefixIRI	DOID:0050177
prefLabel	简单遗传疾病
seeAlso	URI: http://www.ebi.ac.uk/cellline#simple_genetic_disease
引自	http://purl.obolibrary.org/obo/clo.owl
标签	简单遗传疾病
subClassOf	http://purl.obolibrary.org/obo/DOID_630

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Mapping To	Ontology	Source
http://purl.obolibrary.org/obo/DOID_0050177	International Classification of Diseases Ontology	SAME_URI
http://purl.obolibrary.org/obo/DOID_0050177	Cell Line Ontology Subset for Chinese National Infrastructure of Cell Line Resource (NICR)	SAME_URI
http://purl.obolibrary.org/obo/DOID_0050177	Human Disease Ontology 123	SAME_URI