Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP2189.RAXuVQ4N3Zsrx7jM5BOVPNSY3r_-rZD-F2vl2d-Nujor0130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_curated type ECO_0000205 NP2189.RAXuVQ4N3Zsrx7jM5BOVPNSY3r_-rZD-F2vl2d-Nujor0130_provenance.
- source_evidence_curated label "DisGeNET evidence - CURATED" NP2189.RAXuVQ4N3Zsrx7jM5BOVPNSY3r_-rZD-F2vl2d-Nujor0130_provenance.
- source_evidence_curated comment "Gene-disease associations manually curated." NP2189.RAXuVQ4N3Zsrx7jM5BOVPNSY3r_-rZD-F2vl2d-Nujor0130_provenance.
- NP2189.RAXuVQ4N3Zsrx7jM5BOVPNSY3r_-rZD-F2vl2d-Nujor0130_assertion description "[Fas (CD95/Apo-1) mutations were previously reported as the genetic defect responsible for human lymphoproliferative syndrome associated with autoimmune manifestations (also known as autoimmune lymphoproliferative syndrome or Canale-Smith syndrome).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP2189.RAXuVQ4N3Zsrx7jM5BOVPNSY3r_-rZD-F2vl2d-Nujor0130_provenance.
- NP2189.RAXuVQ4N3Zsrx7jM5BOVPNSY3r_-rZD-F2vl2d-Nujor0130_assertion evidence source_evidence_curated NP2189.RAXuVQ4N3Zsrx7jM5BOVPNSY3r_-rZD-F2vl2d-Nujor0130_provenance.
- NP2189.RAXuVQ4N3Zsrx7jM5BOVPNSY3r_-rZD-F2vl2d-Nujor0130_assertion SIO_000772 10515860 NP2189.RAXuVQ4N3Zsrx7jM5BOVPNSY3r_-rZD-F2vl2d-Nujor0130_provenance.
- NP2189.RAXuVQ4N3Zsrx7jM5BOVPNSY3r_-rZD-F2vl2d-Nujor0130_assertion wasDerivedFrom uniprot-20130724 NP2189.RAXuVQ4N3Zsrx7jM5BOVPNSY3r_-rZD-F2vl2d-Nujor0130_provenance.
- NP2189.RAXuVQ4N3Zsrx7jM5BOVPNSY3r_-rZD-F2vl2d-Nujor0130_assertion wasGeneratedBy ECO_0000218 NP2189.RAXuVQ4N3Zsrx7jM5BOVPNSY3r_-rZD-F2vl2d-Nujor0130_provenance.
- uniprot-20130724 importedOn "2013-07-24" NP2189.RAXuVQ4N3Zsrx7jM5BOVPNSY3r_-rZD-F2vl2d-Nujor0130_provenance.