Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP1383177.RA-vIIxycLEyE1FLBEbr407mbS04SAif4biae6tiWtq1A130_assertion> ?p ?o ?g. }
Showing items 1 to 6 of
6
with 100 items per page.
- NP1383177.RA-vIIxycLEyE1FLBEbr407mbS04SAif4biae6tiWtq1A130_assertion type Assertion NP1383177.RA-vIIxycLEyE1FLBEbr407mbS04SAif4biae6tiWtq1A130_head.
- NP1383177.RA-vIIxycLEyE1FLBEbr407mbS04SAif4biae6tiWtq1A130_assertion wasGeneratedBy ECO_0000203 NP1383177.RA-vIIxycLEyE1FLBEbr407mbS04SAif4biae6tiWtq1A130_provenance.
- NP1383177.RA-vIIxycLEyE1FLBEbr407mbS04SAif4biae6tiWtq1A130_assertion wasDerivedFrom befree-2016 NP1383177.RA-vIIxycLEyE1FLBEbr407mbS04SAif4biae6tiWtq1A130_provenance.
- NP1383177.RA-vIIxycLEyE1FLBEbr407mbS04SAif4biae6tiWtq1A130_assertion SIO_000772 9354764 NP1383177.RA-vIIxycLEyE1FLBEbr407mbS04SAif4biae6tiWtq1A130_provenance.
- NP1383177.RA-vIIxycLEyE1FLBEbr407mbS04SAif4biae6tiWtq1A130_assertion evidence source_evidence_literature NP1383177.RA-vIIxycLEyE1FLBEbr407mbS04SAif4biae6tiWtq1A130_provenance.
- NP1383177.RA-vIIxycLEyE1FLBEbr407mbS04SAif4biae6tiWtq1A130_assertion description "[Familial amyloidosis of the Finnish type (FAF) is an autosomal dominant type of systemic amyloidosis caused by a G654A (Asn-187) or G654T (Tyr-187) mutation in the gelsolin gene.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1383177.RA-vIIxycLEyE1FLBEbr407mbS04SAif4biae6tiWtq1A130_provenance.