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- source_evidence_literature type ECO_0000212 NP523717.RAv8jnsXcWs4B2uE-zP1-wW0_-xNN5WhV9kcDcIo1D0dE130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP523717.RAv8jnsXcWs4B2uE-zP1-wW0_-xNN5WhV9kcDcIo1D0dE130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP523717.RAv8jnsXcWs4B2uE-zP1-wW0_-xNN5WhV9kcDcIo1D0dE130_provenance.
- NP523717.RAv8jnsXcWs4B2uE-zP1-wW0_-xNN5WhV9kcDcIo1D0dE130_assertion wasGeneratedBy ECO_0000203 NP523717.RAv8jnsXcWs4B2uE-zP1-wW0_-xNN5WhV9kcDcIo1D0dE130_provenance.
- NP523717.RAv8jnsXcWs4B2uE-zP1-wW0_-xNN5WhV9kcDcIo1D0dE130_assertion wasDerivedFrom befree-20140225 NP523717.RAv8jnsXcWs4B2uE-zP1-wW0_-xNN5WhV9kcDcIo1D0dE130_provenance.
- NP523717.RAv8jnsXcWs4B2uE-zP1-wW0_-xNN5WhV9kcDcIo1D0dE130_assertion SIO_000772 18317533 NP523717.RAv8jnsXcWs4B2uE-zP1-wW0_-xNN5WhV9kcDcIo1D0dE130_provenance.
- NP523717.RAv8jnsXcWs4B2uE-zP1-wW0_-xNN5WhV9kcDcIo1D0dE130_assertion evidence source_evidence_literature NP523717.RAv8jnsXcWs4B2uE-zP1-wW0_-xNN5WhV9kcDcIo1D0dE130_provenance.
- NP523717.RAv8jnsXcWs4B2uE-zP1-wW0_-xNN5WhV9kcDcIo1D0dE130_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." NP523717.RAv8jnsXcWs4B2uE-zP1-wW0_-xNN5WhV9kcDcIo1D0dE130_provenance.
- befree-20140225 importedOn "2014-02-25" NP523717.RAv8jnsXcWs4B2uE-zP1-wW0_-xNN5WhV9kcDcIo1D0dE130_provenance.