Matches in Nanopublications for { ?s ?p "[These results expand the phenotypic spectrum associated with PAX2 mutations, which have been shown to lead to congenital abnormalities of the kidney and urinary tract as part of papillorenal syndrome.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine."@en ?g. }
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- NP609354.RAdvSNz8TYJ7gKZpyQpYnr0t2UeNl_Tvhvy_wlWg6ZdGU130_assertion description "[These results expand the phenotypic spectrum associated with PAX2 mutations, which have been shown to lead to congenital abnormalities of the kidney and urinary tract as part of papillorenal syndrome.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP609354.RAdvSNz8TYJ7gKZpyQpYnr0t2UeNl_Tvhvy_wlWg6ZdGU130_provenance.
- assertion description "[These results expand the phenotypic spectrum associated with PAX2 mutations, which have been shown to lead to congenital abnormalities of the kidney and urinary tract as part of papillorenal syndrome.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.
- assertion description "[These results expand the phenotypic spectrum associated with PAX2 mutations, which have been shown to lead to congenital abnormalities of the kidney and urinary tract as part of papillorenal syndrome.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.
- assertion description "[These results expand the phenotypic spectrum associated with PAX2 mutations, which have been shown to lead to congenital abnormalities of the kidney and urinary tract as part of papillorenal syndrome.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.
- NP7833.RATpZvGF8m636RoGMawLpl0zKgKC5o4wKIGUy8IAZgN0w130_assertion description "[These results expand the phenotypic spectrum associated with PAX2 mutations, which have been shown to lead to congenital abnormalities of the kidney and urinary tract as part of papillorenal syndrome.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP7833.RATpZvGF8m636RoGMawLpl0zKgKC5o4wKIGUy8IAZgN0w130_provenance.
- NP1168178.RAfoPXsuL54JvBCVrcc1gVhcNe2e5iUg_NzE7yw5L-sbc130_assertion description "[These results expand the phenotypic spectrum associated with PAX2 mutations, which have been shown to lead to congenital abnormalities of the kidney and urinary tract as part of papillorenal syndrome.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1168178.RAfoPXsuL54JvBCVrcc1gVhcNe2e5iUg_NzE7yw5L-sbc130_provenance.
- NP609147.RA-9Ix4xUwRYwhsxRvrwCwy2Fvmr_-3UPaELmsK6DDK6M130_assertion description "[These results expand the phenotypic spectrum associated with PAX2 mutations, which have been shown to lead to congenital abnormalities of the kidney and urinary tract as part of papillorenal syndrome.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP609147.RA-9Ix4xUwRYwhsxRvrwCwy2Fvmr_-3UPaELmsK6DDK6M130_provenance.
- NP1168179.RA51SLMX-IQC6Wo0QZFfgSEVUo8jgnAtim9qjJuP_7j38130_assertion description "[These results expand the phenotypic spectrum associated with PAX2 mutations, which have been shown to lead to congenital abnormalities of the kidney and urinary tract as part of papillorenal syndrome.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1168179.RA51SLMX-IQC6Wo0QZFfgSEVUo8jgnAtim9qjJuP_7j38130_provenance.