Open cmungall opened 9 years ago
Why not use Disease Ontology for cancer terms ?
On Mon, Sep 21, 2015 at 11:08 AM, Chris Mungall notifications@github.com wrote:
See @drseb https://github.com/drseb's question here: obophenotype/human-phenotype-ontology#473 (comment) https://github.com/obophenotype/human-phenotype-ontology/issues/473#issuecomment-142003070
Briefly:
- MP cancer terms typically refer to disposition
- HP cancer terms refer to an actual material object and or process in a patient (although there are 2 related syns that pertain to disposition)
We would like to use NCIt. How? Need to be careful of ontological commitments. NCIt cancers are under 'finding'. We strictly segregate disease and phenotype. If we use the same class in both contexts (we will most likely switch NCIt classes into mondo) then trouble will ensue
— Reply to this email directly or view it on GitHub https://github.com/obophenotype/upheno/issues/145.
Suggest: We should reference the disease entities to DO and the phenotypic feature (the actual tumour) to HP and we need to decide what semantics the NCI terms have, i.e., are they closer to HP (finding) or are they closer to DO (disease). -Peter
If it is helpful, DO also contains tumor terms, our terms are aligned to NCIt terms.
Cheers, Lynn
NCIT is the authority here, prefer to get what we need there and all the rest of us pull from there? But, here we are discussing phenotypes not diseases.
Yes, we need a strategy to (1) migrate and (2) rescue old annotations and maybe (3) wrap the terms in xrefs so as to make downstream software insulated from changes etc
NCIt classes are axiomatized, links back to cells, anatomy etc (which we would rewire to uberon/cl)
I had also assumed that NCIt more complete for cancer. What is the long term plan for integration?
DO is working directly with NCIt, to integrate their terms which are not yet in DO. We are working on a set of ~300 terms identified by NCI as potentially novel for DO.
Please note that every Neoplasm in NCIT is a subclass of Disease or Disorder, which is problematic for HP/MP.
this is slowly progressing. @cmungall @mellybelly do we have someone actively working on this?
See @drseb's question here: https://github.com/obophenotype/human-phenotype-ontology/issues/473#issuecomment-142003070
Briefly:
We would like to use NCIt. How? Need to be careful of ontological commitments. NCIt cancers are under 'finding'. We strictly segregate disease and phenotype. If we use the same class in both contexts (we will most likely switch NCIt classes into mondo) then trouble will ensue