Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP2081.RArA9WgdlO5fAQ-bQ3MW8TBpOtKsgHorjeSpo2gS9nI6E130_provenance>. }
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- source_evidence_curated type ECO_0000205 NP2081.RArA9WgdlO5fAQ-bQ3MW8TBpOtKsgHorjeSpo2gS9nI6E130_provenance.
- source_evidence_curated label "DisGeNET evidence - CURATED" NP2081.RArA9WgdlO5fAQ-bQ3MW8TBpOtKsgHorjeSpo2gS9nI6E130_provenance.
- source_evidence_curated comment "Gene-disease associations manually curated." NP2081.RArA9WgdlO5fAQ-bQ3MW8TBpOtKsgHorjeSpo2gS9nI6E130_provenance.
- NP2081.RArA9WgdlO5fAQ-bQ3MW8TBpOtKsgHorjeSpo2gS9nI6E130_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." NP2081.RArA9WgdlO5fAQ-bQ3MW8TBpOtKsgHorjeSpo2gS9nI6E130_provenance.
- NP2081.RArA9WgdlO5fAQ-bQ3MW8TBpOtKsgHorjeSpo2gS9nI6E130_assertion evidence source_evidence_curated NP2081.RArA9WgdlO5fAQ-bQ3MW8TBpOtKsgHorjeSpo2gS9nI6E130_provenance.
- NP2081.RArA9WgdlO5fAQ-bQ3MW8TBpOtKsgHorjeSpo2gS9nI6E130_assertion SIO_000772 10515860 NP2081.RArA9WgdlO5fAQ-bQ3MW8TBpOtKsgHorjeSpo2gS9nI6E130_provenance.
- NP2081.RArA9WgdlO5fAQ-bQ3MW8TBpOtKsgHorjeSpo2gS9nI6E130_assertion wasDerivedFrom uniprot-20150221 NP2081.RArA9WgdlO5fAQ-bQ3MW8TBpOtKsgHorjeSpo2gS9nI6E130_provenance.
- NP2081.RArA9WgdlO5fAQ-bQ3MW8TBpOtKsgHorjeSpo2gS9nI6E130_assertion wasGeneratedBy ECO_0000218 NP2081.RArA9WgdlO5fAQ-bQ3MW8TBpOtKsgHorjeSpo2gS9nI6E130_provenance.
- uniprot-20150221 importedOn "2015-02-21" NP2081.RArA9WgdlO5fAQ-bQ3MW8TBpOtKsgHorjeSpo2gS9nI6E130_provenance.