Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP520153.RAipMKi5ch2aoUX8VIgNh2u2XLYpSTV4C9GBywGYkwoq0130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP520153.RAipMKi5ch2aoUX8VIgNh2u2XLYpSTV4C9GBywGYkwoq0130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP520153.RAipMKi5ch2aoUX8VIgNh2u2XLYpSTV4C9GBywGYkwoq0130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP520153.RAipMKi5ch2aoUX8VIgNh2u2XLYpSTV4C9GBywGYkwoq0130_provenance.
- NP520153.RAipMKi5ch2aoUX8VIgNh2u2XLYpSTV4C9GBywGYkwoq0130_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." NP520153.RAipMKi5ch2aoUX8VIgNh2u2XLYpSTV4C9GBywGYkwoq0130_provenance.
- NP520153.RAipMKi5ch2aoUX8VIgNh2u2XLYpSTV4C9GBywGYkwoq0130_assertion evidence source_evidence_literature NP520153.RAipMKi5ch2aoUX8VIgNh2u2XLYpSTV4C9GBywGYkwoq0130_provenance.
- NP520153.RAipMKi5ch2aoUX8VIgNh2u2XLYpSTV4C9GBywGYkwoq0130_assertion SIO_000772 20309000 NP520153.RAipMKi5ch2aoUX8VIgNh2u2XLYpSTV4C9GBywGYkwoq0130_provenance.
- NP520153.RAipMKi5ch2aoUX8VIgNh2u2XLYpSTV4C9GBywGYkwoq0130_assertion wasDerivedFrom befree-20140225 NP520153.RAipMKi5ch2aoUX8VIgNh2u2XLYpSTV4C9GBywGYkwoq0130_provenance.
- NP520153.RAipMKi5ch2aoUX8VIgNh2u2XLYpSTV4C9GBywGYkwoq0130_assertion wasGeneratedBy ECO_0000203 NP520153.RAipMKi5ch2aoUX8VIgNh2u2XLYpSTV4C9GBywGYkwoq0130_provenance.
- befree-20140225 importedOn "2014-02-25" NP520153.RAipMKi5ch2aoUX8VIgNh2u2XLYpSTV4C9GBywGYkwoq0130_provenance.