Matches in Nanopublications for { ?s ?p "[OCA type 2 (OCA2), the most common form of OCA, is an autosomal recessive disorder caused by mutations in the P gene, the function(s) of which is controversial.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine."@en ?g. }
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- NP394612.RAFFhrzQ7bHmiFhH0yMuY3HUs5mNOyP7owQl5Qw2-weIc130_assertion description "[OCA type 2 (OCA2), the most common form of OCA, is an autosomal recessive disorder caused by mutations in the P gene, the function(s) of which is controversial.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP394612.RAFFhrzQ7bHmiFhH0yMuY3HUs5mNOyP7owQl5Qw2-weIc130_provenance.
- NP355809.RA4PdopcfNwtRnn03dfX7zH4E5yoF0mHxgorJ6iAuOKqA130_assertion description "[OCA type 2 (OCA2), the most common form of OCA, is an autosomal recessive disorder caused by mutations in the P gene, the function(s) of which is controversial.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP355809.RA4PdopcfNwtRnn03dfX7zH4E5yoF0mHxgorJ6iAuOKqA130_provenance.