Matches in Nanopublications for { ?s ?p "[Papillorenal syndrome is an autosomal dominant entity due to PAX2 gene mutation, involving optic nerve and renal malformations.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine."@en ?g. }
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- NP250852.RANtwYne9v2HGr3KxHJ0TRyGjMglxk1mdcSMRX3alR_lw130_assertion description "[Papillorenal syndrome is an autosomal dominant entity due to PAX2 gene mutation, involving optic nerve and renal malformations.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP250852.RANtwYne9v2HGr3KxHJ0TRyGjMglxk1mdcSMRX3alR_lw130_provenance.