Matches in Nanopublications for { <http://rdf.disgenet.org/nanopublications.trig#NP534150.RA3gzyZix9nGwG4IUgZyntITMgcnFzCJX6RWz89MdX6IA130_assertion> ?p ?o ?g. }
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- NP534150.RA3gzyZix9nGwG4IUgZyntITMgcnFzCJX6RWz89MdX6IA130_assertion type Assertion NP534150.RA3gzyZix9nGwG4IUgZyntITMgcnFzCJX6RWz89MdX6IA130_head.
- NP534150.RA3gzyZix9nGwG4IUgZyntITMgcnFzCJX6RWz89MdX6IA130_assertion description "[Based upon the unique finding of the mutation and the expression of CRYAA in the lens, this R21L mutation in the CRYAA is considered to be causative for the dominant cataract phenotype.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP534150.RA3gzyZix9nGwG4IUgZyntITMgcnFzCJX6RWz89MdX6IA130_provenance.
- NP534150.RA3gzyZix9nGwG4IUgZyntITMgcnFzCJX6RWz89MdX6IA130_assertion evidence source_evidence_literature NP534150.RA3gzyZix9nGwG4IUgZyntITMgcnFzCJX6RWz89MdX6IA130_provenance.
- NP534150.RA3gzyZix9nGwG4IUgZyntITMgcnFzCJX6RWz89MdX6IA130_assertion SIO_000772 16453125 NP534150.RA3gzyZix9nGwG4IUgZyntITMgcnFzCJX6RWz89MdX6IA130_provenance.
- NP534150.RA3gzyZix9nGwG4IUgZyntITMgcnFzCJX6RWz89MdX6IA130_assertion wasDerivedFrom befree-20140225 NP534150.RA3gzyZix9nGwG4IUgZyntITMgcnFzCJX6RWz89MdX6IA130_provenance.
- NP534150.RA3gzyZix9nGwG4IUgZyntITMgcnFzCJX6RWz89MdX6IA130_assertion wasGeneratedBy ECO_0000203 NP534150.RA3gzyZix9nGwG4IUgZyntITMgcnFzCJX6RWz89MdX6IA130_provenance.