Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP865242.RAkFYRdYs6UR6ZmAjR1F9ZdaXgXdC-HvHwtoGIjnsoe68130_assertion> ?p ?o ?g. }
Showing items 1 to 6 of
6
with 100 items per page.
- NP865242.RAkFYRdYs6UR6ZmAjR1F9ZdaXgXdC-HvHwtoGIjnsoe68130_assertion type Assertion NP865242.RAkFYRdYs6UR6ZmAjR1F9ZdaXgXdC-HvHwtoGIjnsoe68130_head.
- NP865242.RAkFYRdYs6UR6ZmAjR1F9ZdaXgXdC-HvHwtoGIjnsoe68130_assertion wasGeneratedBy ECO_0000203 NP865242.RAkFYRdYs6UR6ZmAjR1F9ZdaXgXdC-HvHwtoGIjnsoe68130_provenance.
- NP865242.RAkFYRdYs6UR6ZmAjR1F9ZdaXgXdC-HvHwtoGIjnsoe68130_assertion wasDerivedFrom befree-2016 NP865242.RAkFYRdYs6UR6ZmAjR1F9ZdaXgXdC-HvHwtoGIjnsoe68130_provenance.
- NP865242.RAkFYRdYs6UR6ZmAjR1F9ZdaXgXdC-HvHwtoGIjnsoe68130_assertion SIO_000772 21233288 NP865242.RAkFYRdYs6UR6ZmAjR1F9ZdaXgXdC-HvHwtoGIjnsoe68130_provenance.
- NP865242.RAkFYRdYs6UR6ZmAjR1F9ZdaXgXdC-HvHwtoGIjnsoe68130_assertion evidence source_evidence_literature NP865242.RAkFYRdYs6UR6ZmAjR1F9ZdaXgXdC-HvHwtoGIjnsoe68130_provenance.
- NP865242.RAkFYRdYs6UR6ZmAjR1F9ZdaXgXdC-HvHwtoGIjnsoe68130_assertion description "[Mutation of the inositol polyphosphate 5-phosphatase OCRL1 results in two disorders in humans, namely Lowe syndrome (characterized by ocular, nervous system, and renal defects) and type 2 Dent disease (in which only the renal symptoms are evident).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP865242.RAkFYRdYs6UR6ZmAjR1F9ZdaXgXdC-HvHwtoGIjnsoe68130_provenance.