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- NP30218.RAQqW_bdH22jz5JqWz_f98_WqLJikMkZ-XLwV-JYQWG0A130_assertion type Assertion NP30218.RAQqW_bdH22jz5JqWz_f98_WqLJikMkZ-XLwV-JYQWG0A130_head.
- NP30218.RAQqW_bdH22jz5JqWz_f98_WqLJikMkZ-XLwV-JYQWG0A130_assertion description "[Mutations at a single codon in Mad homology 2 domain of SMAD4 cause Myhre syndrome.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP30218.RAQqW_bdH22jz5JqWz_f98_WqLJikMkZ-XLwV-JYQWG0A130_provenance.
- NP30218.RAQqW_bdH22jz5JqWz_f98_WqLJikMkZ-XLwV-JYQWG0A130_assertion evidence source_evidence_curated NP30218.RAQqW_bdH22jz5JqWz_f98_WqLJikMkZ-XLwV-JYQWG0A130_provenance.
- NP30218.RAQqW_bdH22jz5JqWz_f98_WqLJikMkZ-XLwV-JYQWG0A130_assertion SIO_000772 22158539 NP30218.RAQqW_bdH22jz5JqWz_f98_WqLJikMkZ-XLwV-JYQWG0A130_provenance.
- NP30218.RAQqW_bdH22jz5JqWz_f98_WqLJikMkZ-XLwV-JYQWG0A130_assertion wasDerivedFrom ctd_human-20130708 NP30218.RAQqW_bdH22jz5JqWz_f98_WqLJikMkZ-XLwV-JYQWG0A130_provenance.
- NP30218.RAQqW_bdH22jz5JqWz_f98_WqLJikMkZ-XLwV-JYQWG0A130_assertion wasGeneratedBy ECO_0000218 NP30218.RAQqW_bdH22jz5JqWz_f98_WqLJikMkZ-XLwV-JYQWG0A130_provenance.