Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP609147.RA-9Ix4xUwRYwhsxRvrwCwy2Fvmr_-3UPaELmsK6DDK6M130_assertion> ?p ?o ?g. }
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- NP609147.RA-9Ix4xUwRYwhsxRvrwCwy2Fvmr_-3UPaELmsK6DDK6M130_assertion type Assertion NP609147.RA-9Ix4xUwRYwhsxRvrwCwy2Fvmr_-3UPaELmsK6DDK6M130_head.
- 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.
- NP609147.RA-9Ix4xUwRYwhsxRvrwCwy2Fvmr_-3UPaELmsK6DDK6M130_assertion evidence source_evidence_literature NP609147.RA-9Ix4xUwRYwhsxRvrwCwy2Fvmr_-3UPaELmsK6DDK6M130_provenance.
- NP609147.RA-9Ix4xUwRYwhsxRvrwCwy2Fvmr_-3UPaELmsK6DDK6M130_assertion SIO_000772 24676634 NP609147.RA-9Ix4xUwRYwhsxRvrwCwy2Fvmr_-3UPaELmsK6DDK6M130_provenance.
- NP609147.RA-9Ix4xUwRYwhsxRvrwCwy2Fvmr_-3UPaELmsK6DDK6M130_assertion wasDerivedFrom befree-20150227 NP609147.RA-9Ix4xUwRYwhsxRvrwCwy2Fvmr_-3UPaELmsK6DDK6M130_provenance.
- NP609147.RA-9Ix4xUwRYwhsxRvrwCwy2Fvmr_-3UPaELmsK6DDK6M130_assertion wasGeneratedBy ECO_0000203 NP609147.RA-9Ix4xUwRYwhsxRvrwCwy2Fvmr_-3UPaELmsK6DDK6M130_provenance.