Matches in Nanopublications for { ?s ?p "[PCDH21 mutations are not a major cause of the retinal diseases investigated herein, and the corresponding human phenotype remains to be determined.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine."@en ?g. }
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- NP961716.RAaAYMg5S7NyHM7XaCllapdZj4aibzD1k6miNE7GalHPk130_assertion description "[PCDH21 mutations are not a major cause of the retinal diseases investigated herein, and the corresponding human phenotype remains to be determined.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP961716.RAaAYMg5S7NyHM7XaCllapdZj4aibzD1k6miNE7GalHPk130_provenance.
- NP522764.RAw6xQN43xtlhnmkvo1qsi9QPZDfhZ4zzDEsDhArmUh1w130_assertion description "[PCDH21 mutations are not a major cause of the retinal diseases investigated herein, and the corresponding human phenotype remains to be determined.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP522764.RAw6xQN43xtlhnmkvo1qsi9QPZDfhZ4zzDEsDhArmUh1w130_provenance.