Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP458521.RA0NOx6ZbddkyqvpvMpJZAp1L6j_SMsenRCo5la8GlZlU130_assertion> ?p ?o ?g. }
Showing items 1 to 6 of
6
with 100 items per page.
- NP458521.RA0NOx6ZbddkyqvpvMpJZAp1L6j_SMsenRCo5la8GlZlU130_assertion type Assertion NP458521.RA0NOx6ZbddkyqvpvMpJZAp1L6j_SMsenRCo5la8GlZlU130_head.
- NP458521.RA0NOx6ZbddkyqvpvMpJZAp1L6j_SMsenRCo5la8GlZlU130_assertion description "[The missense mutation in exon 13 of the beta MHC gene in individuals with FHCM is associated with high penetrance, highly variable expressivity, severe disease, early in onset and a high incidence of premature sudden death.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP458521.RA0NOx6ZbddkyqvpvMpJZAp1L6j_SMsenRCo5la8GlZlU130_provenance.
- NP458521.RA0NOx6ZbddkyqvpvMpJZAp1L6j_SMsenRCo5la8GlZlU130_assertion evidence source_evidence_literature NP458521.RA0NOx6ZbddkyqvpvMpJZAp1L6j_SMsenRCo5la8GlZlU130_provenance.
- NP458521.RA0NOx6ZbddkyqvpvMpJZAp1L6j_SMsenRCo5la8GlZlU130_assertion SIO_000772 7934006 NP458521.RA0NOx6ZbddkyqvpvMpJZAp1L6j_SMsenRCo5la8GlZlU130_provenance.
- NP458521.RA0NOx6ZbddkyqvpvMpJZAp1L6j_SMsenRCo5la8GlZlU130_assertion wasDerivedFrom befree-20150227 NP458521.RA0NOx6ZbddkyqvpvMpJZAp1L6j_SMsenRCo5la8GlZlU130_provenance.
- NP458521.RA0NOx6ZbddkyqvpvMpJZAp1L6j_SMsenRCo5la8GlZlU130_assertion wasGeneratedBy ECO_0000203 NP458521.RA0NOx6ZbddkyqvpvMpJZAp1L6j_SMsenRCo5la8GlZlU130_provenance.