Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP761618.RAA0fnKIBS2rlKRphzOSSwfKT-x7tRGPzYVDVAMgZ7rNc130_assertion> ?p ?o ?g. }
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- NP761618.RAA0fnKIBS2rlKRphzOSSwfKT-x7tRGPzYVDVAMgZ7rNc130_assertion type Assertion NP761618.RAA0fnKIBS2rlKRphzOSSwfKT-x7tRGPzYVDVAMgZ7rNc130_head.
- 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.
- NP761618.RAA0fnKIBS2rlKRphzOSSwfKT-x7tRGPzYVDVAMgZ7rNc130_assertion evidence source_evidence_literature NP761618.RAA0fnKIBS2rlKRphzOSSwfKT-x7tRGPzYVDVAMgZ7rNc130_provenance.
- NP761618.RAA0fnKIBS2rlKRphzOSSwfKT-x7tRGPzYVDVAMgZ7rNc130_assertion SIO_000772 23797140 NP761618.RAA0fnKIBS2rlKRphzOSSwfKT-x7tRGPzYVDVAMgZ7rNc130_provenance.
- NP761618.RAA0fnKIBS2rlKRphzOSSwfKT-x7tRGPzYVDVAMgZ7rNc130_assertion wasDerivedFrom befree-20150227 NP761618.RAA0fnKIBS2rlKRphzOSSwfKT-x7tRGPzYVDVAMgZ7rNc130_provenance.
- NP761618.RAA0fnKIBS2rlKRphzOSSwfKT-x7tRGPzYVDVAMgZ7rNc130_assertion wasGeneratedBy ECO_0000203 NP761618.RAA0fnKIBS2rlKRphzOSSwfKT-x7tRGPzYVDVAMgZ7rNc130_provenance.