Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP741210.RASRqYE7Vhu_RagKGguG0Io85Uh2FWCDgGa31PioxQ88g130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP741210.RASRqYE7Vhu_RagKGguG0Io85Uh2FWCDgGa31PioxQ88g130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP741210.RASRqYE7Vhu_RagKGguG0Io85Uh2FWCDgGa31PioxQ88g130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP741210.RASRqYE7Vhu_RagKGguG0Io85Uh2FWCDgGa31PioxQ88g130_provenance.
- NP741210.RASRqYE7Vhu_RagKGguG0Io85Uh2FWCDgGa31PioxQ88g130_assertion description "[An 8-months-old male infant with a mutation in the polyadenylation site of FOXP3 gene, absence of FOXP3 protein expression and clinical manifestations of IPEX syndrome, including eczema, colitis, failure to thrive, TPN requirement, and elevated serum IgE, underwent matched unrelated hematopoietic stem cell transplant.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP741210.RASRqYE7Vhu_RagKGguG0Io85Uh2FWCDgGa31PioxQ88g130_provenance.
- NP741210.RASRqYE7Vhu_RagKGguG0Io85Uh2FWCDgGa31PioxQ88g130_assertion evidence source_evidence_literature NP741210.RASRqYE7Vhu_RagKGguG0Io85Uh2FWCDgGa31PioxQ88g130_provenance.
- NP741210.RASRqYE7Vhu_RagKGguG0Io85Uh2FWCDgGa31PioxQ88g130_assertion SIO_000772 19471859 NP741210.RASRqYE7Vhu_RagKGguG0Io85Uh2FWCDgGa31PioxQ88g130_provenance.
- NP741210.RASRqYE7Vhu_RagKGguG0Io85Uh2FWCDgGa31PioxQ88g130_assertion wasDerivedFrom befree-2016 NP741210.RASRqYE7Vhu_RagKGguG0Io85Uh2FWCDgGa31PioxQ88g130_provenance.
- NP741210.RASRqYE7Vhu_RagKGguG0Io85Uh2FWCDgGa31PioxQ88g130_assertion wasGeneratedBy ECO_0000203 NP741210.RASRqYE7Vhu_RagKGguG0Io85Uh2FWCDgGa31PioxQ88g130_provenance.
- befree-2016 importedOn "2016-02-19" NP741210.RASRqYE7Vhu_RagKGguG0Io85Uh2FWCDgGa31PioxQ88g130_provenance.