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Why is HP:phenotypic abormality so different from MP:phenotypic abnormality? #7
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I think those other sets of ancestors may have been from a previous version of Phenio (the following is from v2023-07-11).
None of those pesky CARO or UBERON terms. Still not completely parallel, since HP:0000118 -> BFO:0000001 has to traverse UPHENO:0001005 and UPHENO:0001002.
The shortest path between the two is still short: ['MP:0000001', 'UPHENO:0001003', 'UPHENO:0001005', 'HP:0000118'] but this is also part of the path between all HP and MP nodes without other shared UPHENO terms in PHENIO. My point being that there is additional distance to cover in the cross-phenotype comparisons, semsim or otherwise. |
Excellent @caufieldjh. Sorry I didnt realise you made that analysis already in this ticket. I guess then CARO/UBERON was not really taken into account, right? Lets stick with this example here for a minute. Ok, to restate the problem: When using a lattice, we create a lot of parallel hierarchies, like HPO:All is a distinct parent of HP:PA and not of MP:PA. When using the equivalence model, MP:PA would automatically get HP:PA as a parent. Now the question is: is that desireable? I don't know either way right now. If the polyhierarchies are not harmonised (which they are not), the lattice models would result in a large amount of distance between terms which would have been virtually identical after the equivalence model. cc @souzadevinicius this is going to be the first scientific question we will have to answer! |
In monarch-initiative/semsimian#82 (comment)
@caufieldjh showed us that HP:phenotypic abnormality is very different parents than MP:phenotypic abnormality.
Can we determine why? In particular, why does the HP term have Uberon ancestors?
@caufieldjh I will assign you for now, but feel free to talk to Chris and assign someone else - it is easier for me to work if I can assign while creating the ticket so I am sure its not dropping of the radar.
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