Matches in Nanopublications for { ?s ?p "[On the basis of the present data, and the nearly identical clinical and/or pathological phenotype of the other reported cases of congenital NCL, it is reasonable to suggest that cathepsin D deficiency caused by mutations in the corresponding gene may underlie all cases of congenital NCL.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine."@en ?g. }
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- assertion description "[On the basis of the present data, and the nearly identical clinical and/or pathological phenotype of the other reported cases of congenital NCL, it is reasonable to suggest that cathepsin D deficiency caused by mutations in the corresponding gene may underlie all cases of congenital NCL.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.
- NP337495.RAVbzBc15LMcyiC7R1ZUIcHPYpBvxQ7ZEAGUdQPHipQqA130_assertion description "[On the basis of the present data, and the nearly identical clinical and/or pathological phenotype of the other reported cases of congenital NCL, it is reasonable to suggest that cathepsin D deficiency caused by mutations in the corresponding gene may underlie all cases of congenital NCL.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP337495.RAVbzBc15LMcyiC7R1ZUIcHPYpBvxQ7ZEAGUdQPHipQqA130_provenance.
- NP547974.RAZLKfUvj2JtyN_mvD6qkAv26FMsMdTsRqor0X45XxuF0130_assertion description "[On the basis of the present data, and the nearly identical clinical and/or pathological phenotype of the other reported cases of congenital NCL, it is reasonable to suggest that cathepsin D deficiency caused by mutations in the corresponding gene may underlie all cases of congenital NCL.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP547974.RAZLKfUvj2JtyN_mvD6qkAv26FMsMdTsRqor0X45XxuF0130_provenance.