Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP865241.RAAJN3l6TYN5t72vqHNtMl42lKQuDwcV4dYz46RmdOnlQ130_assertion> ?p ?o ?g. }
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- NP865241.RAAJN3l6TYN5t72vqHNtMl42lKQuDwcV4dYz46RmdOnlQ130_assertion type Assertion NP865241.RAAJN3l6TYN5t72vqHNtMl42lKQuDwcV4dYz46RmdOnlQ130_head.
- NP865241.RAAJN3l6TYN5t72vqHNtMl42lKQuDwcV4dYz46RmdOnlQ130_assertion wasGeneratedBy ECO_0000203 NP865241.RAAJN3l6TYN5t72vqHNtMl42lKQuDwcV4dYz46RmdOnlQ130_provenance.
- NP865241.RAAJN3l6TYN5t72vqHNtMl42lKQuDwcV4dYz46RmdOnlQ130_assertion wasDerivedFrom befree-2016 NP865241.RAAJN3l6TYN5t72vqHNtMl42lKQuDwcV4dYz46RmdOnlQ130_provenance.
- NP865241.RAAJN3l6TYN5t72vqHNtMl42lKQuDwcV4dYz46RmdOnlQ130_assertion SIO_000772 21233288 NP865241.RAAJN3l6TYN5t72vqHNtMl42lKQuDwcV4dYz46RmdOnlQ130_provenance.
- NP865241.RAAJN3l6TYN5t72vqHNtMl42lKQuDwcV4dYz46RmdOnlQ130_assertion evidence source_evidence_literature NP865241.RAAJN3l6TYN5t72vqHNtMl42lKQuDwcV4dYz46RmdOnlQ130_provenance.
- NP865241.RAAJN3l6TYN5t72vqHNtMl42lKQuDwcV4dYz46RmdOnlQ130_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." NP865241.RAAJN3l6TYN5t72vqHNtMl42lKQuDwcV4dYz46RmdOnlQ130_provenance.