Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP436940.RA0JwTLJYJwLM2P7UX0lMGa1PgoMyEUHZhTGaSmJ0OpqI130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP436940.RA0JwTLJYJwLM2P7UX0lMGa1PgoMyEUHZhTGaSmJ0OpqI130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP436940.RA0JwTLJYJwLM2P7UX0lMGa1PgoMyEUHZhTGaSmJ0OpqI130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP436940.RA0JwTLJYJwLM2P7UX0lMGa1PgoMyEUHZhTGaSmJ0OpqI130_provenance.
- befree-20150227 importedOn "2015-02-27" NP436940.RA0JwTLJYJwLM2P7UX0lMGa1PgoMyEUHZhTGaSmJ0OpqI130_provenance.
- 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.