Category:BGT Molecular Abnormality(B4083)
From BiomedGT
BGT_Molecular Abnormality(B4083)
Lexical
Concept Code: B4083
(N)
Preferred Name: Molecular Abnormality
Coding Scheme: BGT (09.06a )
Synonym: Molecular Abnormality (PT) (Source: NCI) / Chromosomal, Gene, or Protein Abnormality (SY) (Source: NCI) / Cytogenetic or Molecular Genetic Abnormality (SY) (Source: NCI) / Genetic Abnormality (SY) (Source: NCI)
Definition: Abnormalities that occur in human cells and tissues and models of human cancer. (Source: NCI)
URI: http://ncicb.nci.nih.gov/xml/owl/EVS/BiomedGT.owl#B4083
Properties
Semantic_Type: Cell or Molecular Dysfunction
NCI_META_CUI: CL347298
Associations
Parent: OWL_Thing (primitive)
Form:LexWiki_BGT_Form
Facts about BGT Molecular Abnormality(B4083)RDF feed
| BGT Concept Type(P365) | N + |
| BGT NCI META CUI(P208) | CL347298 +info.pngNCI META CUI lookup |
| BGT Semantic Type(P106) | Cell or Molecular Dysfunction +info.pngSemantic Type lookup |
| BGT Synonym(P104) | Molecular Abnormality +, Chromosomal, Gene, or Protein Abnormality +, Cytogenetic or Molecular Genetic Abnormality +, and Genetic Abnormality + |
| DCTerms hasVersion(hasVersion) | BGT/Versions/09.06a + |
| Has default form | LexWiki BGT Form + |
| LexWiki Concept Code | B4083 + |
| LexWiki Definition | Abnormalities that occur in human cells and tissues and models of human cancer. (Source: NCI) |
| LexWiki Preferred Name | Molecular Abnormality + |
| LexWiki URI | http://ncicb.nci.nih.gov/xml/owl/EVS/BiomedGT.owl#B4083 + |
| SKOS inScheme(inScheme) | BGT + |
Subcategories
There are 3 subcategories to this category.
