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Matches in Nanopublications for { ?s ?p "[Familial amyloid polyneuropathy (FAP; also known as familiar amyloidosis and hereditary amyloidosis) is an autosomal dominant inherited disease due to mutations of the transthyretin (TTR) gene coding for the corresponding protein, consisting of 127 amino acids.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine."@en ?g. }

• NP199053.RAVevFtB1DbE_lez9dZU5A7kru5Jg5lYokF3aUYQD1YuM130_assertion description "[Familial amyloid polyneuropathy (FAP; also known as familiar amyloidosis and hereditary amyloidosis) is an autosomal dominant inherited disease due to mutations of the transthyretin (TTR) gene coding for the corresponding protein, consisting of 127 amino acids.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP199053.RAVevFtB1DbE_lez9dZU5A7kru5Jg5lYokF3aUYQD1YuM130_provenance.
• NP830350.RAeWE4RTkF9oOKY1lCOscrScR1rsCUwxgzw13FMD8fE-4130_assertion description "[Familial amyloid polyneuropathy (FAP; also known as familiar amyloidosis and hereditary amyloidosis) is an autosomal dominant inherited disease due to mutations of the transthyretin (TTR) gene coding for the corresponding protein, consisting of 127 amino acids.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP830350.RAeWE4RTkF9oOKY1lCOscrScR1rsCUwxgzw13FMD8fE-4130_provenance.
• NP213606.RA8L6eNMEKnRIBl86LE6AIpbMognWRRDTozRiVF_Hy8sw130_assertion description "[Familial amyloid polyneuropathy (FAP; also known as familiar amyloidosis and hereditary amyloidosis) is an autosomal dominant inherited disease due to mutations of the transthyretin (TTR) gene coding for the corresponding protein, consisting of 127 amino acids.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP213606.RA8L6eNMEKnRIBl86LE6AIpbMognWRRDTozRiVF_Hy8sw130_provenance.
• NP864971.RAgtLIJlJFF1vm05TtpNUbICWu6bpI_PSCeHicqiFTYVs130_assertion description "[Familial amyloid polyneuropathy (FAP; also known as familiar amyloidosis and hereditary amyloidosis) is an autosomal dominant inherited disease due to mutations of the transthyretin (TTR) gene coding for the corresponding protein, consisting of 127 amino acids.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP864971.RAgtLIJlJFF1vm05TtpNUbICWu6bpI_PSCeHicqiFTYVs130_provenance.
• NP379144.RAajaEj0u8wO5Twx1L_62zImy2P583L7qQHpO_1GCmRzY130_assertion description "[Familial amyloid polyneuropathy (FAP; also known as familiar amyloidosis and hereditary amyloidosis) is an autosomal dominant inherited disease due to mutations of the transthyretin (TTR) gene coding for the corresponding protein, consisting of 127 amino acids.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP379144.RAajaEj0u8wO5Twx1L_62zImy2P583L7qQHpO_1GCmRzY130_provenance.
• NP561675.RAoC9_2Dt16G7gROazVUaA3X27ySg_xVub_e5mB4beJ-U130_assertion description "[Familial amyloid polyneuropathy (FAP; also known as familiar amyloidosis and hereditary amyloidosis) is an autosomal dominant inherited disease due to mutations of the transthyretin (TTR) gene coding for the corresponding protein, consisting of 127 amino acids.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP561675.RAoC9_2Dt16G7gROazVUaA3X27ySg_xVub_e5mB4beJ-U130_provenance.
• NP751557.RAu2BmiVLDly81GoKe65a-MR7nohUGdyIyAQ8DNYwm-jA130_assertion description "[Familial amyloid polyneuropathy (FAP; also known as familiar amyloidosis and hereditary amyloidosis) is an autosomal dominant inherited disease due to mutations of the transthyretin (TTR) gene coding for the corresponding protein, consisting of 127 amino acids.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP751557.RAu2BmiVLDly81GoKe65a-MR7nohUGdyIyAQ8DNYwm-jA130_provenance.
• NP273062.RA8U9r7KReFH6bIT5V7gaRZRmW-3fjaDk1zx1vb4aK6mg130_assertion description "[Familial amyloid polyneuropathy (FAP; also known as familiar amyloidosis and hereditary amyloidosis) is an autosomal dominant inherited disease due to mutations of the transthyretin (TTR) gene coding for the corresponding protein, consisting of 127 amino acids.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP273062.RA8U9r7KReFH6bIT5V7gaRZRmW-3fjaDk1zx1vb4aK6mg130_provenance.
• NP788375.RAfRB6hOdvK3fXI1SCI1XqgajH5H6OBYi_jAJd6THM8po130_assertion description "[Familial amyloid polyneuropathy (FAP; also known as familiar amyloidosis and hereditary amyloidosis) is an autosomal dominant inherited disease due to mutations of the transthyretin (TTR) gene coding for the corresponding protein, consisting of 127 amino acids.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP788375.RAfRB6hOdvK3fXI1SCI1XqgajH5H6OBYi_jAJd6THM8po130_provenance.
• NP521195.RA_C0l5jF0ylKUdtcvg8mqdjCuRtxIcihHMBcsBWxAtCM130_assertion description "[Familial amyloid polyneuropathy (FAP; also known as familiar amyloidosis and hereditary amyloidosis) is an autosomal dominant inherited disease due to mutations of the transthyretin (TTR) gene coding for the corresponding protein, consisting of 127 amino acids.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP521195.RA_C0l5jF0ylKUdtcvg8mqdjCuRtxIcihHMBcsBWxAtCM130_provenance.
• NP776093.RA2S_QmYbbzYTXpyMdKlZWHs80fzS0B1hq-U5MXF9bpwY130_assertion description "[Familial amyloid polyneuropathy (FAP; also known as familiar amyloidosis and hereditary amyloidosis) is an autosomal dominant inherited disease due to mutations of the transthyretin (TTR) gene coding for the corresponding protein, consisting of 127 amino acids.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP776093.RA2S_QmYbbzYTXpyMdKlZWHs80fzS0B1hq-U5MXF9bpwY130_provenance.
• NP722928.RA1FsIAooly-XyP2HCfqa5VC8dqmn9ycf2nQc7889tHBM130_assertion description "[Familial amyloid polyneuropathy (FAP; also known as familiar amyloidosis and hereditary amyloidosis) is an autosomal dominant inherited disease due to mutations of the transthyretin (TTR) gene coding for the corresponding protein, consisting of 127 amino acids.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP722928.RA1FsIAooly-XyP2HCfqa5VC8dqmn9ycf2nQc7889tHBM130_provenance.
• NP761719.RAvAgJ8sWaxvWL2HUK4iusyDu3l9sRmKtH7JI-jD5cgjg130_assertion description "[Familial amyloid polyneuropathy (FAP; also known as familiar amyloidosis and hereditary amyloidosis) is an autosomal dominant inherited disease due to mutations of the transthyretin (TTR) gene coding for the corresponding protein, consisting of 127 amino acids.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP761719.RAvAgJ8sWaxvWL2HUK4iusyDu3l9sRmKtH7JI-jD5cgjg130_provenance.
• NP761736.RAl4PcdpqW36rSVwuewbSFTxLi1xHUUu9PMLOlkfrcBQs130_assertion description "[Familial amyloid polyneuropathy (FAP; also known as familiar amyloidosis and hereditary amyloidosis) is an autosomal dominant inherited disease due to mutations of the transthyretin (TTR) gene coding for the corresponding protein, consisting of 127 amino acids.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP761736.RAl4PcdpqW36rSVwuewbSFTxLi1xHUUu9PMLOlkfrcBQs130_provenance.
• NP761618.RAA0fnKIBS2rlKRphzOSSwfKT-x7tRGPzYVDVAMgZ7rNc130_assertion description "[Familial amyloid polyneuropathy (FAP; also known as familiar amyloidosis and hereditary amyloidosis) is an autosomal dominant inherited disease due to mutations of the transthyretin (TTR) gene coding for the corresponding protein, consisting of 127 amino acids.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP761618.RAA0fnKIBS2rlKRphzOSSwfKT-x7tRGPzYVDVAMgZ7rNc130_provenance.
• NP1088638.RAu01qTHc5cH1Vc3AK21lwPQZopMdPdQGZMq_lwa1VRNo130_assertion description "[Familial amyloid polyneuropathy (FAP; also known as familiar amyloidosis and hereditary amyloidosis) is an autosomal dominant inherited disease due to mutations of the transthyretin (TTR) gene coding for the corresponding protein, consisting of 127 amino acids.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1088638.RAu01qTHc5cH1Vc3AK21lwPQZopMdPdQGZMq_lwa1VRNo130_provenance.
• NP1088640.RAtSBEA3SmXcnI2YAVrs9gHd07ILBctT4Af9x2Sqpc7GA130_assertion description "[Familial amyloid polyneuropathy (FAP; also known as familiar amyloidosis and hereditary amyloidosis) is an autosomal dominant inherited disease due to mutations of the transthyretin (TTR) gene coding for the corresponding protein, consisting of 127 amino acids.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1088640.RAtSBEA3SmXcnI2YAVrs9gHd07ILBctT4Af9x2Sqpc7GA130_provenance.
• NP1088639.RA468S2NEacuvV9sis53AWU_gVIGWZddGYQg-tWJg-P-Y130_assertion description "[Familial amyloid polyneuropathy (FAP; also known as familiar amyloidosis and hereditary amyloidosis) is an autosomal dominant inherited disease due to mutations of the transthyretin (TTR) gene coding for the corresponding protein, consisting of 127 amino acids.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1088639.RA468S2NEacuvV9sis53AWU_gVIGWZddGYQg-tWJg-P-Y130_provenance.