Class: Snv
SNVs are single nucleotide positions in genomic DNA at which different sequence alternatives exist
URI: biolink:Snv
classDiagram
class Snv
SequenceVariant <|-- Snv
Snv : category
Snv : description
Snv : full_name
Snv : has_attribute
Snv --|> attribute : has_attribute
Snv : has_biological_sequence
Snv : has_gene
Snv --|> gene : has_gene
Snv : id
Snv : in_taxon
Snv --|> organism taxon : in_taxon
Snv : in_taxon_label
Snv : iri
Snv : name
Snv : provided_by
Snv : synonym
Snv : type
Snv : xref
Inheritance
Slots
| Name | Cardinality and Range | Description | Inheritance |
|---|---|---|---|
| has_gene | 0..* Gene |
Each allele can be associated with any number of genes | SequenceVariant |
| has_biological_sequence | 0..1 BiologicalSequence |
The state of the sequence w | GenomicEntity |
| id | 1..1 String |
A unique identifier for an entity | Entity, OntologyClass |
| in_taxon | 0..* OrganismTaxon |
connects an entity to its taxonomic classification | ThingWithTaxon |
| in_taxon_label | 0..1 LabelType |
The human readable scientific name for the taxon of the entity | ThingWithTaxon |
| provided_by | 0..* String |
The value in this node property represents the knowledge provider that create... | NamedThing |
| xref | 0..* Uriorcurie |
A database cross reference or alternative identifier for a NamedThing or edge... | NamedThing |
| full_name | 0..1 LabelType |
a long-form human readable name for a thing | NamedThing |
| synonym | 0..* LabelType |
Alternate human-readable names for a thing | NamedThing |
| iri | 0..1 IriType |
An IRI for an entity | Entity |
| category | 1..* CategoryType |
Name of the high level ontology class in which this entity is categorized | Entity |
| type | 0..* String |
Entity | |
| name | 0..1 LabelType |
A human-readable name for an attribute or entity | Entity |
| description | 0..1 NarrativeText |
a human-readable description of an entity | Entity |
| has_attribute | 0..* Attribute |
connects any entity to an attribute | Entity |
Aliases
- single nucleotide variant
- single nucleotide polymorphism
- snp
Identifier and Mapping Information
Schema Source
- from schema: https://w3id.org/biolink/biolink-model
Mappings
| Mapping Type | Mapped Value |
|---|---|
| self | biolink:Snv |
| native | biolink:Snv |
| exact | SO:0001483 |
LinkML Source
Direct
name: snv
description: SNVs are single nucleotide positions in genomic DNA at which different
sequence alternatives exist
from_schema: https://w3id.org/biolink/biolink-model
aliases:
- single nucleotide variant
- single nucleotide polymorphism
- snp
exact_mappings:
- SO:0001483
is_a: sequence variant