NIFSTD - sequence_variant - Terms

NIFSTD Summary

Preferred Name (rdfs:label)	sequence_variant
ID	p1:SO_0001060
Full Id	http://purl.org/obo/owl/SO#SO_0001060
hasDefinition	A sequence_variant is a non exact copy of a sequence_feature or genome exhibiting one or more sequence_alteration.
hasOBONamespace	sequence
label	sequence_variant

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Mapping To	Ontology	Source	Relationship	Added By	Added On	Notes
http://ncicb.nci.nih.gov/xml/owl/EVS/Thesaurus.owl#Genetic_Variation	NCI Thesaurus	NCBO (lexical mapping)	skos:closeMatch	loom	04/02/13	View Notes
http://purl.org/obo/owl/SO#SO_0001060	Suggested Ontology for Pharmacogenomics	NCBO (Identical URI)	skos:exactMatch	loom	04/03/13	View Notes
http://purl.obolibrary.org/obo/MAO_0000066	Multiple alignment	NCBO (lexical mapping)	skos:closeMatch	loom	04/02/13	View Notes
http://purl.obolibrary.org/obo/SO_0001060	Sequence types and features	NCBO (lexical mapping)	skos:closeMatch	loom	04/02/13	View Notes
http://purl.org/obo/owl/SO#SO_0001060	SNP-Ontology	NCBO (Identical URI)	skos:exactMatch	loom	04/03/13	View Notes

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