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- NP316379.RAQ4PIhamUZevGfhrjwQRSyptxJZd5ZYQdh4-OWynnBD0130_assertion type Assertion NP316379.RAQ4PIhamUZevGfhrjwQRSyptxJZd5ZYQdh4-OWynnBD0130_head.
- NP316379.RAQ4PIhamUZevGfhrjwQRSyptxJZd5ZYQdh4-OWynnBD0130_assertion wasGeneratedBy ECO_0000203 NP316379.RAQ4PIhamUZevGfhrjwQRSyptxJZd5ZYQdh4-OWynnBD0130_provenance.
- NP316379.RAQ4PIhamUZevGfhrjwQRSyptxJZd5ZYQdh4-OWynnBD0130_assertion wasDerivedFrom befree-20140225 NP316379.RAQ4PIhamUZevGfhrjwQRSyptxJZd5ZYQdh4-OWynnBD0130_provenance.
- NP316379.RAQ4PIhamUZevGfhrjwQRSyptxJZd5ZYQdh4-OWynnBD0130_assertion SIO_000772 9354764 NP316379.RAQ4PIhamUZevGfhrjwQRSyptxJZd5ZYQdh4-OWynnBD0130_provenance.
- NP316379.RAQ4PIhamUZevGfhrjwQRSyptxJZd5ZYQdh4-OWynnBD0130_assertion evidence source_evidence_literature NP316379.RAQ4PIhamUZevGfhrjwQRSyptxJZd5ZYQdh4-OWynnBD0130_provenance.
- NP316379.RAQ4PIhamUZevGfhrjwQRSyptxJZd5ZYQdh4-OWynnBD0130_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." NP316379.RAQ4PIhamUZevGfhrjwQRSyptxJZd5ZYQdh4-OWynnBD0130_provenance.