Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP436940.RA0JwTLJYJwLM2P7UX0lMGa1PgoMyEUHZhTGaSmJ0OpqI130_assertion> ?p ?o ?g. }
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- NP436940.RA0JwTLJYJwLM2P7UX0lMGa1PgoMyEUHZhTGaSmJ0OpqI130_assertion type Assertion NP436940.RA0JwTLJYJwLM2P7UX0lMGa1PgoMyEUHZhTGaSmJ0OpqI130_head.
- NP436940.RA0JwTLJYJwLM2P7UX0lMGa1PgoMyEUHZhTGaSmJ0OpqI130_assertion wasGeneratedBy ECO_0000203 NP436940.RA0JwTLJYJwLM2P7UX0lMGa1PgoMyEUHZhTGaSmJ0OpqI130_provenance.
- NP436940.RA0JwTLJYJwLM2P7UX0lMGa1PgoMyEUHZhTGaSmJ0OpqI130_assertion wasDerivedFrom befree-20150227 NP436940.RA0JwTLJYJwLM2P7UX0lMGa1PgoMyEUHZhTGaSmJ0OpqI130_provenance.
- NP436940.RA0JwTLJYJwLM2P7UX0lMGa1PgoMyEUHZhTGaSmJ0OpqI130_assertion SIO_000772 16258946 NP436940.RA0JwTLJYJwLM2P7UX0lMGa1PgoMyEUHZhTGaSmJ0OpqI130_provenance.
- NP436940.RA0JwTLJYJwLM2P7UX0lMGa1PgoMyEUHZhTGaSmJ0OpqI130_assertion evidence source_evidence_literature NP436940.RA0JwTLJYJwLM2P7UX0lMGa1PgoMyEUHZhTGaSmJ0OpqI130_provenance.
- NP436940.RA0JwTLJYJwLM2P7UX0lMGa1PgoMyEUHZhTGaSmJ0OpqI130_assertion description "[Familial amyloidosis of the Finnish type (FAF) is a rare autosomal-dominant disorder caused by the accumulation of a 71-amino acid amyloidogenic fragment of mutant gelsolin, an actin-modulating protein.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP436940.RA0JwTLJYJwLM2P7UX0lMGa1PgoMyEUHZhTGaSmJ0OpqI130_provenance.