Matches in Nanopublications for { ?s ?p "[Tyrosinase-related oculocutaneous albinism (OCA1), an autosomal recessive inborn error of pigmentation, is caused by the deficiency of tyrosinase.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine."@en ?g. }
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- NP168365.RAMxn6Kh9rFIr789JbHnOHhtpIOlq_coidu6C6ozcNEm0130_assertion description "[Tyrosinase-related oculocutaneous albinism (OCA1), an autosomal recessive inborn error of pigmentation, is caused by the deficiency of tyrosinase.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP168365.RAMxn6Kh9rFIr789JbHnOHhtpIOlq_coidu6C6ozcNEm0130_provenance.
- assertion description "[Tyrosinase-related oculocutaneous albinism (OCA1), an autosomal recessive inborn error of pigmentation, is caused by the deficiency of tyrosinase.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.
- NP1393789.RAkpJgS3P7cRBLeugER53tPRXRUfgIgvTYC7qAhWfc1DE130_assertion description "[Tyrosinase-related oculocutaneous albinism (OCA1), an autosomal recessive inborn error of pigmentation, is caused by the deficiency of tyrosinase.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1393789.RAkpJgS3P7cRBLeugER53tPRXRUfgIgvTYC7qAhWfc1DE130_provenance.