Matches in Nanopublications for { <http://rdf.disgenet.org/nanopublications.trig#NP2189.RAXuVQ4N3Zsrx7jM5BOVPNSY3r_-rZD-F2vl2d-Nujor0130_assertion> ?p ?o ?g. }
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- NP2189.RAXuVQ4N3Zsrx7jM5BOVPNSY3r_-rZD-F2vl2d-Nujor0130_assertion type Assertion NP2189.RAXuVQ4N3Zsrx7jM5BOVPNSY3r_-rZD-F2vl2d-Nujor0130_head.
- 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.