Tom Conlin

[My initial look at the data](https://gist.github.com/TomConlin/4392fc172dc2023bda7cf6f0f5d0f280) notes: - I do not like the biological patents. - Alleles need a difference from reference component - consider per chromosome alleles. - Anatomy/Tissue...

if I recall they touch on ~600 species

The statements I see associated with OMIA_000284-9825 post refactor are below; still do not include a disease label but might that not best come in best through a clique merge...

in other cases the OMIA may be linked with OMIM

filtering redundant phenotypes as early as possible is key. on the server in solr would be ideal because then you would not transmit them but even making each list a...

to capture what a disease is annotated to, we would have to distinguish the terms from all their included ancestors. converting to a set means HP:0000118 shows up once per...

I am content with once. I don't get a new grandparent through each of my cousins.

It could be interesting to look at from the phenotype ancestor "score card" point of view. but you still would not compute over them just split out a count to...

The curie_map.yaml has the purl `http://purl.obolibrary.org/obo/OMIA_`' as the expansion https://github.com/monarch-initiative/dipper/blob/master/dipper/curie_map.yaml#L52 the persistent URL base http://purl.obolibrary.org/obo/ has moved to: http://purl.oclc.org/obo/ which has moved to: http://www.berkeleybop.org/ontologies/ which has nothing obvious related to...

Confirming this bug is still in the download .deb mid May 2017