Matches in Nanopublications for { ?s ?p "[OTX2 mutations cause autosomal dominant pattern dystrophy of the retinal pigment epithelium.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine."@en ?g. }
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- assertion description "[OTX2 mutations cause autosomal dominant pattern dystrophy of the retinal pigment epithelium.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.
- NP8033.RAW4OoQZFrcAgedAWasN4_4mhstNYncYBeGr940O5ThrE130_assertion description "[OTX2 mutations cause autosomal dominant pattern dystrophy of the retinal pigment epithelium.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP8033.RAW4OoQZFrcAgedAWasN4_4mhstNYncYBeGr940O5ThrE130_provenance.