Matches in Nanopublications for { <http://rdf.disgenet.org/nanopublications.trig#NP864971.RAgtLIJlJFF1vm05TtpNUbICWu6bpI_PSCeHicqiFTYVs130_assertion> ?p ?o ?g. }
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- NP864971.RAgtLIJlJFF1vm05TtpNUbICWu6bpI_PSCeHicqiFTYVs130_assertion type Assertion NP864971.RAgtLIJlJFF1vm05TtpNUbICWu6bpI_PSCeHicqiFTYVs130_head.
- 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.
- NP864971.RAgtLIJlJFF1vm05TtpNUbICWu6bpI_PSCeHicqiFTYVs130_assertion evidence source_evidence_literature NP864971.RAgtLIJlJFF1vm05TtpNUbICWu6bpI_PSCeHicqiFTYVs130_provenance.
- NP864971.RAgtLIJlJFF1vm05TtpNUbICWu6bpI_PSCeHicqiFTYVs130_assertion SIO_000772 23797140 NP864971.RAgtLIJlJFF1vm05TtpNUbICWu6bpI_PSCeHicqiFTYVs130_provenance.
- NP864971.RAgtLIJlJFF1vm05TtpNUbICWu6bpI_PSCeHicqiFTYVs130_assertion wasDerivedFrom befree-20140225 NP864971.RAgtLIJlJFF1vm05TtpNUbICWu6bpI_PSCeHicqiFTYVs130_provenance.
- NP864971.RAgtLIJlJFF1vm05TtpNUbICWu6bpI_PSCeHicqiFTYVs130_assertion wasGeneratedBy ECO_0000203 NP864971.RAgtLIJlJFF1vm05TtpNUbICWu6bpI_PSCeHicqiFTYVs130_provenance.