Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP927797.RAsQ0lh7nbP03Yttk6sO88Ix_CGWRk1XMxMMa84iwNoLU130_assertion> ?p ?o ?g. }
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- NP927797.RAsQ0lh7nbP03Yttk6sO88Ix_CGWRk1XMxMMa84iwNoLU130_assertion type Assertion NP927797.RAsQ0lh7nbP03Yttk6sO88Ix_CGWRk1XMxMMa84iwNoLU130_head.
- NP927797.RAsQ0lh7nbP03Yttk6sO88Ix_CGWRk1XMxMMa84iwNoLU130_assertion description "[Screening all exons of CPA6 in unrelated patients with partial epilepsy (n = 195) and FS (n = 145) revealed a new heterozygous missense mutation c.799G>A (p.Gly267Arg) in three TLE patients.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP927797.RAsQ0lh7nbP03Yttk6sO88Ix_CGWRk1XMxMMa84iwNoLU130_provenance.
- NP927797.RAsQ0lh7nbP03Yttk6sO88Ix_CGWRk1XMxMMa84iwNoLU130_assertion evidence source_evidence_literature NP927797.RAsQ0lh7nbP03Yttk6sO88Ix_CGWRk1XMxMMa84iwNoLU130_provenance.
- NP927797.RAsQ0lh7nbP03Yttk6sO88Ix_CGWRk1XMxMMa84iwNoLU130_assertion SIO_000772 21922598 NP927797.RAsQ0lh7nbP03Yttk6sO88Ix_CGWRk1XMxMMa84iwNoLU130_provenance.
- NP927797.RAsQ0lh7nbP03Yttk6sO88Ix_CGWRk1XMxMMa84iwNoLU130_assertion wasDerivedFrom befree-20150227 NP927797.RAsQ0lh7nbP03Yttk6sO88Ix_CGWRk1XMxMMa84iwNoLU130_provenance.
- NP927797.RAsQ0lh7nbP03Yttk6sO88Ix_CGWRk1XMxMMa84iwNoLU130_assertion wasGeneratedBy ECO_0000203 NP927797.RAsQ0lh7nbP03Yttk6sO88Ix_CGWRk1XMxMMa84iwNoLU130_provenance.