Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP436885.RA073voAQ_CviO_o_2ViWtnmu-7jJLK5xmv__1yisqyOU130_assertion> ?p ?o ?g. }
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- NP436885.RA073voAQ_CviO_o_2ViWtnmu-7jJLK5xmv__1yisqyOU130_assertion type Assertion NP436885.RA073voAQ_CviO_o_2ViWtnmu-7jJLK5xmv__1yisqyOU130_head.
- NP436885.RA073voAQ_CviO_o_2ViWtnmu-7jJLK5xmv__1yisqyOU130_assertion wasGeneratedBy ECO_0000203 NP436885.RA073voAQ_CviO_o_2ViWtnmu-7jJLK5xmv__1yisqyOU130_provenance.
- NP436885.RA073voAQ_CviO_o_2ViWtnmu-7jJLK5xmv__1yisqyOU130_assertion wasDerivedFrom befree-20150227 NP436885.RA073voAQ_CviO_o_2ViWtnmu-7jJLK5xmv__1yisqyOU130_provenance.
- NP436885.RA073voAQ_CviO_o_2ViWtnmu-7jJLK5xmv__1yisqyOU130_assertion SIO_000772 9354764 NP436885.RA073voAQ_CviO_o_2ViWtnmu-7jJLK5xmv__1yisqyOU130_provenance.
- NP436885.RA073voAQ_CviO_o_2ViWtnmu-7jJLK5xmv__1yisqyOU130_assertion evidence source_evidence_literature NP436885.RA073voAQ_CviO_o_2ViWtnmu-7jJLK5xmv__1yisqyOU130_provenance.
- NP436885.RA073voAQ_CviO_o_2ViWtnmu-7jJLK5xmv__1yisqyOU130_assertion description "[Familial amyloidosis of the Finnish type (FAF) is an autosomal dominant type of systemic amyloidosis caused by a G654A (Asn-187) or G654T (Tyr-187) mutation in the gelsolin gene.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP436885.RA073voAQ_CviO_o_2ViWtnmu-7jJLK5xmv__1yisqyOU130_provenance.