Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP651254.RAWK1KM-1rcSqTXDJ5ZEJO0g_TvOgT9Hp2tMWDJwG3Pak130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP651254.RAWK1KM-1rcSqTXDJ5ZEJO0g_TvOgT9Hp2tMWDJwG3Pak130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP651254.RAWK1KM-1rcSqTXDJ5ZEJO0g_TvOgT9Hp2tMWDJwG3Pak130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP651254.RAWK1KM-1rcSqTXDJ5ZEJO0g_TvOgT9Hp2tMWDJwG3Pak130_provenance.
- NP651254.RAWK1KM-1rcSqTXDJ5ZEJO0g_TvOgT9Hp2tMWDJwG3Pak130_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." NP651254.RAWK1KM-1rcSqTXDJ5ZEJO0g_TvOgT9Hp2tMWDJwG3Pak130_provenance.
- NP651254.RAWK1KM-1rcSqTXDJ5ZEJO0g_TvOgT9Hp2tMWDJwG3Pak130_assertion evidence source_evidence_literature NP651254.RAWK1KM-1rcSqTXDJ5ZEJO0g_TvOgT9Hp2tMWDJwG3Pak130_provenance.
- NP651254.RAWK1KM-1rcSqTXDJ5ZEJO0g_TvOgT9Hp2tMWDJwG3Pak130_assertion SIO_000772 19471859 NP651254.RAWK1KM-1rcSqTXDJ5ZEJO0g_TvOgT9Hp2tMWDJwG3Pak130_provenance.
- NP651254.RAWK1KM-1rcSqTXDJ5ZEJO0g_TvOgT9Hp2tMWDJwG3Pak130_assertion wasDerivedFrom befree-20140225 NP651254.RAWK1KM-1rcSqTXDJ5ZEJO0g_TvOgT9Hp2tMWDJwG3Pak130_provenance.
- NP651254.RAWK1KM-1rcSqTXDJ5ZEJO0g_TvOgT9Hp2tMWDJwG3Pak130_assertion wasGeneratedBy ECO_0000203 NP651254.RAWK1KM-1rcSqTXDJ5ZEJO0g_TvOgT9Hp2tMWDJwG3Pak130_provenance.
- befree-20140225 importedOn "2014-02-25" NP651254.RAWK1KM-1rcSqTXDJ5ZEJO0g_TvOgT9Hp2tMWDJwG3Pak130_provenance.