Matches in Nanopublications for { ?s ?p "[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."@en ?g. }
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- 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.
- 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." provenance.
- NP534203.RAWl7wpuw6XMD0_ETjNYcfC27QFYdc5-MIQFfTRpI1hTY130_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." NP534203.RAWl7wpuw6XMD0_ETjNYcfC27QFYdc5-MIQFfTRpI1hTY130_provenance.
- NP534199.RApVgBP-F3ovfSPSmwjuZUnBpmHY7PmWtO6-4gRNOOJoM130_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." NP534199.RApVgBP-F3ovfSPSmwjuZUnBpmHY7PmWtO6-4gRNOOJoM130_provenance.