Matches in Nanopublications for { ?s ?p "[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."@en ?g. }
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- NP316379.RAQ4PIhamUZevGfhrjwQRSyptxJZd5ZYQdh4-OWynnBD0130_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." NP316379.RAQ4PIhamUZevGfhrjwQRSyptxJZd5ZYQdh4-OWynnBD0130_provenance.
- NP552385.RAsG6yFaP8DDVrGWeRgKQgSK3CeUEXWce05blMjwkkrB0130_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." NP552385.RAsG6yFaP8DDVrGWeRgKQgSK3CeUEXWce05blMjwkkrB0130_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.
- 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." provenance.
- 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." provenance.
- NP1383176.RAyFoXgzloUcJwn-mYrLKmlUxTMQl4oyzL5QBmuYsNYA0130_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." NP1383176.RAyFoXgzloUcJwn-mYrLKmlUxTMQl4oyzL5QBmuYsNYA0130_provenance.
- NP1383177.RA-vIIxycLEyE1FLBEbr407mbS04SAif4biae6tiWtq1A130_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." NP1383177.RA-vIIxycLEyE1FLBEbr407mbS04SAif4biae6tiWtq1A130_provenance.
- NP436877.RAlF8RXJr_HczGwJiihI55XChpv5Ycw5T_ibyXiIGJd7M130_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." NP436877.RAlF8RXJr_HczGwJiihI55XChpv5Ycw5T_ibyXiIGJd7M130_provenance.