Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP834226.RAgHaBqfG728WRn3Nup91rsD3bl8uGLNETUw0WxoxKYDg130_assertion> ?p ?o ?g. }
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- NP834226.RAgHaBqfG728WRn3Nup91rsD3bl8uGLNETUw0WxoxKYDg130_assertion type Assertion NP834226.RAgHaBqfG728WRn3Nup91rsD3bl8uGLNETUw0WxoxKYDg130_head.
- NP834226.RAgHaBqfG728WRn3Nup91rsD3bl8uGLNETUw0WxoxKYDg130_assertion description "[Mutations in SCO2 are associated with a distinct form of hypertrophic cardiomyopathy and cytochrome c oxidase deficiency.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP834226.RAgHaBqfG728WRn3Nup91rsD3bl8uGLNETUw0WxoxKYDg130_provenance.
- NP834226.RAgHaBqfG728WRn3Nup91rsD3bl8uGLNETUw0WxoxKYDg130_assertion evidence source_evidence_literature NP834226.RAgHaBqfG728WRn3Nup91rsD3bl8uGLNETUw0WxoxKYDg130_provenance.
- NP834226.RAgHaBqfG728WRn3Nup91rsD3bl8uGLNETUw0WxoxKYDg130_assertion SIO_000772 10749987 NP834226.RAgHaBqfG728WRn3Nup91rsD3bl8uGLNETUw0WxoxKYDg130_provenance.
- NP834226.RAgHaBqfG728WRn3Nup91rsD3bl8uGLNETUw0WxoxKYDg130_assertion wasDerivedFrom befree-20150227 NP834226.RAgHaBqfG728WRn3Nup91rsD3bl8uGLNETUw0WxoxKYDg130_provenance.
- NP834226.RAgHaBqfG728WRn3Nup91rsD3bl8uGLNETUw0WxoxKYDg130_assertion wasGeneratedBy ECO_0000203 NP834226.RAgHaBqfG728WRn3Nup91rsD3bl8uGLNETUw0WxoxKYDg130_provenance.