snv(?V) is nondet

V is a single nucleotide variant (SNV)

 reference_allele(?V, ?A) is nondet

single nucleotide variant V has reference allele A

 alternative_allele(?V, ?A) is nondet

single nucleotide variant V has alternative allele A

 snv_interpreted_condition(?V, ?C) is nondet

single nucleotide variant V has ClinVar's interpreted condition C

 frequency(F) is nondet

F is instance of tgvo:Frequency

 snv_frequency(?V, ?D, ?F) is nondet

single nucleotide variant V in dataset D has frequency F

 snv_japanese_frequency(?V, ?RA, ?AA, ?D, ?F) is nondet

single nucleotide variant V with reference allele RA and alternative allele AA in dataset D has frequency F (example) pl2sparql -u sparqlprog/ontologies/togovar -s togovar "snv_japanese_frequency(togovar:tgv1006196,"T","C",D,F)" "h(D,F)"

Undocumented predicates

The following predicates are exported, but not or incorrectly documented.

 snv_with_clinvar(Arg1, Arg2, Arg3, Arg4, Arg5)

 dataset(Arg1, Arg2)