Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP899442.RA6dc_IwT63yUeKOKC-ivYC2n_VyVv2wEx1x4f4L6HiRs130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP899442.RA6dc_IwT63yUeKOKC-ivYC2n_VyVv2wEx1x4f4L6HiRs130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP899442.RA6dc_IwT63yUeKOKC-ivYC2n_VyVv2wEx1x4f4L6HiRs130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP899442.RA6dc_IwT63yUeKOKC-ivYC2n_VyVv2wEx1x4f4L6HiRs130_provenance.
- NP899442.RA6dc_IwT63yUeKOKC-ivYC2n_VyVv2wEx1x4f4L6HiRs130_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." NP899442.RA6dc_IwT63yUeKOKC-ivYC2n_VyVv2wEx1x4f4L6HiRs130_provenance.
- NP899442.RA6dc_IwT63yUeKOKC-ivYC2n_VyVv2wEx1x4f4L6HiRs130_assertion evidence source_evidence_literature NP899442.RA6dc_IwT63yUeKOKC-ivYC2n_VyVv2wEx1x4f4L6HiRs130_provenance.
- NP899442.RA6dc_IwT63yUeKOKC-ivYC2n_VyVv2wEx1x4f4L6HiRs130_assertion SIO_000772 20309000 NP899442.RA6dc_IwT63yUeKOKC-ivYC2n_VyVv2wEx1x4f4L6HiRs130_provenance.
- NP899442.RA6dc_IwT63yUeKOKC-ivYC2n_VyVv2wEx1x4f4L6HiRs130_assertion wasDerivedFrom befree-20150227 NP899442.RA6dc_IwT63yUeKOKC-ivYC2n_VyVv2wEx1x4f4L6HiRs130_provenance.
- NP899442.RA6dc_IwT63yUeKOKC-ivYC2n_VyVv2wEx1x4f4L6HiRs130_assertion wasGeneratedBy ECO_0000203 NP899442.RA6dc_IwT63yUeKOKC-ivYC2n_VyVv2wEx1x4f4L6HiRs130_provenance.
- befree-20150227 importedOn "2015-02-27" NP899442.RA6dc_IwT63yUeKOKC-ivYC2n_VyVv2wEx1x4f4L6HiRs130_provenance.