Matches in Nanopublications for { <http://rdf.disgenet.org/nanopublications.trig#NP722928.RA1FsIAooly-XyP2HCfqa5VC8dqmn9ycf2nQc7889tHBM130_assertion> ?p ?o ?g. }
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- NP722928.RA1FsIAooly-XyP2HCfqa5VC8dqmn9ycf2nQc7889tHBM130_assertion type Assertion NP722928.RA1FsIAooly-XyP2HCfqa5VC8dqmn9ycf2nQc7889tHBM130_head.
- 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.
- NP722928.RA1FsIAooly-XyP2HCfqa5VC8dqmn9ycf2nQc7889tHBM130_assertion evidence source_evidence_literature NP722928.RA1FsIAooly-XyP2HCfqa5VC8dqmn9ycf2nQc7889tHBM130_provenance.
- NP722928.RA1FsIAooly-XyP2HCfqa5VC8dqmn9ycf2nQc7889tHBM130_assertion SIO_000772 23797140 NP722928.RA1FsIAooly-XyP2HCfqa5VC8dqmn9ycf2nQc7889tHBM130_provenance.
- NP722928.RA1FsIAooly-XyP2HCfqa5VC8dqmn9ycf2nQc7889tHBM130_assertion wasDerivedFrom befree-20140225 NP722928.RA1FsIAooly-XyP2HCfqa5VC8dqmn9ycf2nQc7889tHBM130_provenance.
- NP722928.RA1FsIAooly-XyP2HCfqa5VC8dqmn9ycf2nQc7889tHBM130_assertion wasGeneratedBy ECO_0000203 NP722928.RA1FsIAooly-XyP2HCfqa5VC8dqmn9ycf2nQc7889tHBM130_provenance.