Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP458521.RA0NOx6ZbddkyqvpvMpJZAp1L6j_SMsenRCo5la8GlZlU130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP458521.RA0NOx6ZbddkyqvpvMpJZAp1L6j_SMsenRCo5la8GlZlU130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP458521.RA0NOx6ZbddkyqvpvMpJZAp1L6j_SMsenRCo5la8GlZlU130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP458521.RA0NOx6ZbddkyqvpvMpJZAp1L6j_SMsenRCo5la8GlZlU130_provenance.
- 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.
- befree-20150227 importedOn "2015-02-27" NP458521.RA0NOx6ZbddkyqvpvMpJZAp1L6j_SMsenRCo5la8GlZlU130_provenance.