Matches in Nanopublications for { ?s ?p "[The phenotype of Severe Early Childhood Onset Retinal Dystrophy (SECORD) from mutation of RPE65 and differentiation from Leber congenital amaurosis.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine."@en ?g. }
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- NP674851.RAbhrXnCS7IXLXMrdtaNHpptcocY2r0KvpzwudEaT2W00130_assertion description "[The phenotype of Severe Early Childhood Onset Retinal Dystrophy (SECORD) from mutation of RPE65 and differentiation from Leber congenital amaurosis.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP674851.RAbhrXnCS7IXLXMrdtaNHpptcocY2r0KvpzwudEaT2W00130_provenance.
- assertion description "[The phenotype of Severe Early Childhood Onset Retinal Dystrophy (SECORD) from mutation of RPE65 and differentiation from Leber congenital amaurosis.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.
- assertion description "[The phenotype of Severe Early Childhood Onset Retinal Dystrophy (SECORD) from mutation of RPE65 and differentiation from Leber congenital amaurosis.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.
- NP836521.RAWoJCjsX-H97z_YRuYD_B6wtXJ4ST9ha8qhxpfJ_ziME130_assertion description "[The phenotype of Severe Early Childhood Onset Retinal Dystrophy (SECORD) from mutation of RPE65 and differentiation from Leber congenital amaurosis.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP836521.RAWoJCjsX-H97z_YRuYD_B6wtXJ4ST9ha8qhxpfJ_ziME130_provenance.