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We don't currently have disease to pathway or any variant data.
Right now the endpoint is a fairly direct representation of the kgx with necessary ontology closure info for indirect lookups, so we're not providing the two hop gene to disease or gene to phenotype via orthology as associations. We do plan to support that again eventually, but haven't yet settled on how.
I couldn't find the following kinds of data in the current API when searching by association-type.
Are they no longer available though this API?
(CC @kevinschaper, related to biothings/biothings_explorer#774)
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