Matches in Nanopublications for { <http://rdf.disgenet.org/nanopublications.trig#NP309201.RA9zDqVF9Uj3vzP4tldJy8xcTM7HcXiUYOA3elasJwmcY130_assertion> ?p ?o ?g. }
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- NP309201.RA9zDqVF9Uj3vzP4tldJy8xcTM7HcXiUYOA3elasJwmcY130_assertion type Assertion NP309201.RA9zDqVF9Uj3vzP4tldJy8xcTM7HcXiUYOA3elasJwmcY130_head.
- NP309201.RA9zDqVF9Uj3vzP4tldJy8xcTM7HcXiUYOA3elasJwmcY130_assertion description "[We describe 2 unrelated patients with IPEX syndrome with a mild clinical phenotype and with novel FOXP3 mutations and the phenotypic and functional characterization of their Treg cells.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP309201.RA9zDqVF9Uj3vzP4tldJy8xcTM7HcXiUYOA3elasJwmcY130_provenance.
- NP309201.RA9zDqVF9Uj3vzP4tldJy8xcTM7HcXiUYOA3elasJwmcY130_assertion evidence source_evidence_literature NP309201.RA9zDqVF9Uj3vzP4tldJy8xcTM7HcXiUYOA3elasJwmcY130_provenance.
- NP309201.RA9zDqVF9Uj3vzP4tldJy8xcTM7HcXiUYOA3elasJwmcY130_assertion SIO_000772 16630773 NP309201.RA9zDqVF9Uj3vzP4tldJy8xcTM7HcXiUYOA3elasJwmcY130_provenance.
- NP309201.RA9zDqVF9Uj3vzP4tldJy8xcTM7HcXiUYOA3elasJwmcY130_assertion wasDerivedFrom befree-20140225 NP309201.RA9zDqVF9Uj3vzP4tldJy8xcTM7HcXiUYOA3elasJwmcY130_provenance.
- NP309201.RA9zDqVF9Uj3vzP4tldJy8xcTM7HcXiUYOA3elasJwmcY130_assertion wasGeneratedBy ECO_0000203 NP309201.RA9zDqVF9Uj3vzP4tldJy8xcTM7HcXiUYOA3elasJwmcY130_provenance.