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- source_evidence_literature type ECO_0000212 NP899432.RAsAgmOLAlzT-PTGPPG_ZZj1kfKnwCi9Sk_t_OmZjfo7c130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP899432.RAsAgmOLAlzT-PTGPPG_ZZj1kfKnwCi9Sk_t_OmZjfo7c130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP899432.RAsAgmOLAlzT-PTGPPG_ZZj1kfKnwCi9Sk_t_OmZjfo7c130_provenance.
- NP899432.RAsAgmOLAlzT-PTGPPG_ZZj1kfKnwCi9Sk_t_OmZjfo7c130_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." NP899432.RAsAgmOLAlzT-PTGPPG_ZZj1kfKnwCi9Sk_t_OmZjfo7c130_provenance.
- NP899432.RAsAgmOLAlzT-PTGPPG_ZZj1kfKnwCi9Sk_t_OmZjfo7c130_assertion evidence source_evidence_literature NP899432.RAsAgmOLAlzT-PTGPPG_ZZj1kfKnwCi9Sk_t_OmZjfo7c130_provenance.
- NP899432.RAsAgmOLAlzT-PTGPPG_ZZj1kfKnwCi9Sk_t_OmZjfo7c130_assertion SIO_000772 20309000 NP899432.RAsAgmOLAlzT-PTGPPG_ZZj1kfKnwCi9Sk_t_OmZjfo7c130_provenance.
- NP899432.RAsAgmOLAlzT-PTGPPG_ZZj1kfKnwCi9Sk_t_OmZjfo7c130_assertion wasDerivedFrom befree-20150227 NP899432.RAsAgmOLAlzT-PTGPPG_ZZj1kfKnwCi9Sk_t_OmZjfo7c130_provenance.
- NP899432.RAsAgmOLAlzT-PTGPPG_ZZj1kfKnwCi9Sk_t_OmZjfo7c130_assertion wasGeneratedBy ECO_0000203 NP899432.RAsAgmOLAlzT-PTGPPG_ZZj1kfKnwCi9Sk_t_OmZjfo7c130_provenance.
- befree-20150227 importedOn "2015-02-27" NP899432.RAsAgmOLAlzT-PTGPPG_ZZj1kfKnwCi9Sk_t_OmZjfo7c130_provenance.