Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP801655.RAi_yWYvuxel3K7bSHbhUYJq8vbPp6gRo8eqjt5dkeBA4130_assertion> ?p ?o ?g. }
Showing items 1 to 6 of
6
with 100 items per page.
- NP801655.RAi_yWYvuxel3K7bSHbhUYJq8vbPp6gRo8eqjt5dkeBA4130_assertion type Assertion NP801655.RAi_yWYvuxel3K7bSHbhUYJq8vbPp6gRo8eqjt5dkeBA4130_head.
- NP801655.RAi_yWYvuxel3K7bSHbhUYJq8vbPp6gRo8eqjt5dkeBA4130_assertion description "[Patients with IPEX (immune dysfunction, polyendocrinopathy, enteropathy, X-linked) syndrome harbor mutations in the forkhead box P3 (FOXP3) gene in regulatory T cells, which leads to severe autoimmunity and immune deficiency.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP801655.RAi_yWYvuxel3K7bSHbhUYJq8vbPp6gRo8eqjt5dkeBA4130_provenance.
- NP801655.RAi_yWYvuxel3K7bSHbhUYJq8vbPp6gRo8eqjt5dkeBA4130_assertion evidence source_evidence_literature NP801655.RAi_yWYvuxel3K7bSHbhUYJq8vbPp6gRo8eqjt5dkeBA4130_provenance.
- NP801655.RAi_yWYvuxel3K7bSHbhUYJq8vbPp6gRo8eqjt5dkeBA4130_assertion SIO_000772 20309000 NP801655.RAi_yWYvuxel3K7bSHbhUYJq8vbPp6gRo8eqjt5dkeBA4130_provenance.
- NP801655.RAi_yWYvuxel3K7bSHbhUYJq8vbPp6gRo8eqjt5dkeBA4130_assertion wasDerivedFrom befree-2016 NP801655.RAi_yWYvuxel3K7bSHbhUYJq8vbPp6gRo8eqjt5dkeBA4130_provenance.
- NP801655.RAi_yWYvuxel3K7bSHbhUYJq8vbPp6gRo8eqjt5dkeBA4130_assertion wasGeneratedBy ECO_0000203 NP801655.RAi_yWYvuxel3K7bSHbhUYJq8vbPp6gRo8eqjt5dkeBA4130_provenance.