About: Insertion Mutation

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An Entity of Type : owl:Class, within Data Space : linked.opendata.cz associated with source document(s)

Attributes	Values
rdf:type	Class
rdfs:label	Insertion Mutation
rdfs:subClassOf	Mutation Abnormality
Semantic_Type	Cell or Molecular Dysfunction
Preferred_Name	Insertion Mutation
UMLS_CUI	C1512796
Legacy_Concept_Name	Insertion_Mutation
FULL_SYN	Insertion MutationSYNCITCGA Insertion MutationPTNCI Mutation, InsertionSYNCI Insertion Mutation AbnormalitySYNCI InsertionSYNCI
DEFINITION	Any rearrangement to the genomic content that adds one or more extra nucleotides into the DNA. Insertions may be reversible, particulary if caused by transposable elements. They may alter the reading frame of a gene, or may cause large scale additions of genomic DNA.NCI
code	C19295
http://linked.open...y/mesh/hasConcept	http://linked.opendata.cz/resource/mesh/concept/M0506943
is someValuesFrom of	nodeID://b655997 nodeID://b656015 nodeID://b656033 nodeID://b656042 nodeID://b656078 nodeID://b656092 nodeID://b656152

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