Matches in Nanopublications for { ?s ?p "[the phenotypic overlap of patients with MEF2C mutations and atypical Rett syndrome is due to the involvement of a common pathway.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine."@en ?g. }
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- NP131185.RA3HCJTSWogDP9AaUTHkv-gKyjhQl6iAyXUCC9ciesVbU130_assertion description "[the phenotypic overlap of patients with MEF2C mutations and atypical Rett syndrome is due to the involvement of a common pathway.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP131185.RA3HCJTSWogDP9AaUTHkv-gKyjhQl6iAyXUCC9ciesVbU130_provenance.
- assertion description "[the phenotypic overlap of patients with MEF2C mutations and atypical Rett syndrome is due to the involvement of a common pathway.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.
- NP177473.RAuJc4F4iDIe7LfipHSQ5SgpKn-qMNDnGQdtM_M6dLN_c130_assertion description "[the phenotypic overlap of patients with MEF2C mutations and atypical Rett syndrome is due to the involvement of a common pathway.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP177473.RAuJc4F4iDIe7LfipHSQ5SgpKn-qMNDnGQdtM_M6dLN_c130_provenance.