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- NP410197.RA2rAL0_wVBNsG6aNhJZQX0eFyApW0wXpxz7HH0ISGTI0130_assertion type Assertion NP410197.RA2rAL0_wVBNsG6aNhJZQX0eFyApW0wXpxz7HH0ISGTI0130_head.
- NP410197.RA2rAL0_wVBNsG6aNhJZQX0eFyApW0wXpxz7HH0ISGTI0130_assertion wasGeneratedBy ECO_0000203 NP410197.RA2rAL0_wVBNsG6aNhJZQX0eFyApW0wXpxz7HH0ISGTI0130_provenance.
- NP410197.RA2rAL0_wVBNsG6aNhJZQX0eFyApW0wXpxz7HH0ISGTI0130_assertion wasDerivedFrom befree-20140225 NP410197.RA2rAL0_wVBNsG6aNhJZQX0eFyApW0wXpxz7HH0ISGTI0130_provenance.
- NP410197.RA2rAL0_wVBNsG6aNhJZQX0eFyApW0wXpxz7HH0ISGTI0130_assertion SIO_000772 18317533 NP410197.RA2rAL0_wVBNsG6aNhJZQX0eFyApW0wXpxz7HH0ISGTI0130_provenance.
- NP410197.RA2rAL0_wVBNsG6aNhJZQX0eFyApW0wXpxz7HH0ISGTI0130_assertion evidence source_evidence_literature NP410197.RA2rAL0_wVBNsG6aNhJZQX0eFyApW0wXpxz7HH0ISGTI0130_provenance.
- NP410197.RA2rAL0_wVBNsG6aNhJZQX0eFyApW0wXpxz7HH0ISGTI0130_assertion description "[Immunodysregulation, polyendocrinopathy, enteropathy, X-linked (IPEX) syndrome is a rare disorder caused by mutations in the FOXP3 gene that result in the defective development of CD4+CD25+ regulatory T cells which constitute an important T cell subset involved in immune homeostasis and protection against autoimmunity.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP410197.RA2rAL0_wVBNsG6aNhJZQX0eFyApW0wXpxz7HH0ISGTI0130_provenance.