Matches in Nanopublications for { <http://rdf.disgenet.org/nanopublications.trig#NP309628.RAaz76RHdtlNZreO8LX7woBkPnA3U7qz0I44xRHAum9nc130_assertion> ?p ?o ?g. }
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- NP309628.RAaz76RHdtlNZreO8LX7woBkPnA3U7qz0I44xRHAum9nc130_assertion type Assertion NP309628.RAaz76RHdtlNZreO8LX7woBkPnA3U7qz0I44xRHAum9nc130_head.
- NP309628.RAaz76RHdtlNZreO8LX7woBkPnA3U7qz0I44xRHAum9nc130_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." NP309628.RAaz76RHdtlNZreO8LX7woBkPnA3U7qz0I44xRHAum9nc130_provenance.
- NP309628.RAaz76RHdtlNZreO8LX7woBkPnA3U7qz0I44xRHAum9nc130_assertion evidence source_evidence_literature NP309628.RAaz76RHdtlNZreO8LX7woBkPnA3U7qz0I44xRHAum9nc130_provenance.
- NP309628.RAaz76RHdtlNZreO8LX7woBkPnA3U7qz0I44xRHAum9nc130_assertion SIO_000772 22158539 NP309628.RAaz76RHdtlNZreO8LX7woBkPnA3U7qz0I44xRHAum9nc130_provenance.
- NP309628.RAaz76RHdtlNZreO8LX7woBkPnA3U7qz0I44xRHAum9nc130_assertion wasDerivedFrom befree-20140225 NP309628.RAaz76RHdtlNZreO8LX7woBkPnA3U7qz0I44xRHAum9nc130_provenance.
- NP309628.RAaz76RHdtlNZreO8LX7woBkPnA3U7qz0I44xRHAum9nc130_assertion wasGeneratedBy ECO_0000203 NP309628.RAaz76RHdtlNZreO8LX7woBkPnA3U7qz0I44xRHAum9nc130_provenance.