Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP1088639.RA468S2NEacuvV9sis53AWU_gVIGWZddGYQg-tWJg-P-Y130_assertion> ?p ?o ?g. }
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- NP1088639.RA468S2NEacuvV9sis53AWU_gVIGWZddGYQg-tWJg-P-Y130_assertion type Assertion NP1088639.RA468S2NEacuvV9sis53AWU_gVIGWZddGYQg-tWJg-P-Y130_head.
- 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.
- NP1088639.RA468S2NEacuvV9sis53AWU_gVIGWZddGYQg-tWJg-P-Y130_assertion evidence source_evidence_literature NP1088639.RA468S2NEacuvV9sis53AWU_gVIGWZddGYQg-tWJg-P-Y130_provenance.
- NP1088639.RA468S2NEacuvV9sis53AWU_gVIGWZddGYQg-tWJg-P-Y130_assertion SIO_000772 23797140 NP1088639.RA468S2NEacuvV9sis53AWU_gVIGWZddGYQg-tWJg-P-Y130_provenance.
- NP1088639.RA468S2NEacuvV9sis53AWU_gVIGWZddGYQg-tWJg-P-Y130_assertion wasDerivedFrom befree-2016 NP1088639.RA468S2NEacuvV9sis53AWU_gVIGWZddGYQg-tWJg-P-Y130_provenance.
- NP1088639.RA468S2NEacuvV9sis53AWU_gVIGWZddGYQg-tWJg-P-Y130_assertion wasGeneratedBy ECO_0000203 NP1088639.RA468S2NEacuvV9sis53AWU_gVIGWZddGYQg-tWJg-P-Y130_provenance.