Matches in Nanopublications for { ?s ?p "[Mutations in the Wilms' tumor suppressor gene (WT1) are linked with Denys-Drash syndrome (DDS), a rare childhood disease characterized by diffuse mesangial sclerosis and renal failure of early onset, XY pseudohermaphroditism, and high risk of Wilms' tumor.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine."@en ?g. }
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- NP471466.RAbBSArsvpt0d0rkmrfWhr8JeS31JIkPRSPYFG5wMmLD4130_assertion description "[Mutations in the Wilms' tumor suppressor gene (WT1) are linked with Denys-Drash syndrome (DDS), a rare childhood disease characterized by diffuse mesangial sclerosis and renal failure of early onset, XY pseudohermaphroditism, and high risk of Wilms' tumor.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP471466.RAbBSArsvpt0d0rkmrfWhr8JeS31JIkPRSPYFG5wMmLD4130_provenance.
- NP199294.RA6vADErbeF0JfqFjInCwUMMOZHFgu29zH0Ak0AhAnwNs130_assertion description "[Mutations in the Wilms' tumor suppressor gene (WT1) are linked with Denys-Drash syndrome (DDS), a rare childhood disease characterized by diffuse mesangial sclerosis and renal failure of early onset, XY pseudohermaphroditism, and high risk of Wilms' tumor.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP199294.RA6vADErbeF0JfqFjInCwUMMOZHFgu29zH0Ak0AhAnwNs130_provenance.
- NP261416.RA77qVYW8q50DSF4TsZOAnNLqYll8UcB7lOST6bI3whcw130_assertion description "[Mutations in the Wilms' tumor suppressor gene (WT1) are linked with Denys-Drash syndrome (DDS), a rare childhood disease characterized by diffuse mesangial sclerosis and renal failure of early onset, XY pseudohermaphroditism, and high risk of Wilms' tumor.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP261416.RA77qVYW8q50DSF4TsZOAnNLqYll8UcB7lOST6bI3whcw130_provenance.