Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP801655.RAi_yWYvuxel3K7bSHbhUYJq8vbPp6gRo8eqjt5dkeBA4130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP801655.RAi_yWYvuxel3K7bSHbhUYJq8vbPp6gRo8eqjt5dkeBA4130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP801655.RAi_yWYvuxel3K7bSHbhUYJq8vbPp6gRo8eqjt5dkeBA4130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP801655.RAi_yWYvuxel3K7bSHbhUYJq8vbPp6gRo8eqjt5dkeBA4130_provenance.
- 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.
- befree-2016 importedOn "2016-02-19" NP801655.RAi_yWYvuxel3K7bSHbhUYJq8vbPp6gRo8eqjt5dkeBA4130_provenance.