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operable program or batch file.
+ D:/Android/ndk-bundle_10/prebuilt/windows-x86_64/bin/make -j 4
/usr/bin/sh: -c: line 1: syntax error: unexpected end of file
log:
Executing tasks: [:gen…
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Currently with DO to OMIM xrefs it isn't clear what should be subclass and what should be equivalent
I suggest we add equivalence axioms to PS IDs where they exist
E.g. http://www.omim.org/phenotypic…
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We have a term that was added in #5261
```yaml
id: MONDO:0800145
name: non-severe combined immunodeficiency due to polymerase delta deficiency
def: "Any non-severe combined immunodeficiency in w…
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- gene-disease annotations should be only for terms defined by the gene causing the disease (e.g ~type1; ...)
- these annotations should come from OMIM only
- the annotation should be brought in ONL…
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I try to index https://github.com/mapsme/omim project.
To do that I create two soft symlinks:
```
$ ls -l ~/bin/rtags/clang
lrwxrwxrwx 1 evgeniy evgeniy 53 сен 22 00:33 /home/evgeniy/bin/rtags/clang …
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Hi! This condition is linked to OMIM 175780 (Brain small vessel disease with or without ocular anomalies). You list the following as synonyms:
- COL4A1-related brain small vessel disease with hemor…
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this disease:
http://monarchinitiative.org/disease/OMIM_608372
http://www.omim.org/entry/608372
this is located to 1q21-q23, and has a "gene" associated with is, that has been given an HGNC identifier…
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https://monarchinitiative.org/disease/OMIM:144010
is a parent of
https://monarchinitiative.org/disease/OMIM:143890
in the emerge network we are trying to settle on an id that is the "group" term for …
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Hello,
The genetic medicine service from the HUG recently reported a patient with a mutation in the gene NOVA2.
Please consider adding the gene to the database and creating a new entity based o…
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Old issues here:
https://github.com/mapsme/omim/issues/4663
https://github.com/mapsme/omim/issues/4819
Reproduced with added POIs here:
First changeset https://www.openstreetmap.org/changeset/1…