Matches in Nanopublications for { ?s ?p "[Non-syndromic oculocutaneous albinism (OCA) is a clinically and genetically heterogeneous autosomal recessive disorder with mutations identified in several genes: OCA1 (tyrosinase, TYR), OCA2 (OCA2), OCA3 (tyrosinase-related protein 1, TYRP1), and OCA4 (membrane-associated transporter protein, MATP).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine."@en ?g. }
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- NP499326.RA2InCX88Ekq0kjjGtBg80ewapPMhJJos6TrwehO1X9-c130_assertion description "[Non-syndromic oculocutaneous albinism (OCA) is a clinically and genetically heterogeneous autosomal recessive disorder with mutations identified in several genes: OCA1 (tyrosinase, TYR), OCA2 (OCA2), OCA3 (tyrosinase-related protein 1, TYRP1), and OCA4 (membrane-associated transporter protein, MATP).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP499326.RA2InCX88Ekq0kjjGtBg80ewapPMhJJos6TrwehO1X9-c130_provenance.
- assertion description "[Non-syndromic oculocutaneous albinism (OCA) is a clinically and genetically heterogeneous autosomal recessive disorder with mutations identified in several genes: OCA1 (tyrosinase, TYR), OCA2 (OCA2), OCA3 (tyrosinase-related protein 1, TYRP1), and OCA4 (membrane-associated transporter protein, MATP).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.
- NP549973.RAAqw27bvGsiY2ZJ_xQ2_Sb3vkrITS7QzoswPgG2WOjBk130_assertion description "[Non-syndromic oculocutaneous albinism (OCA) is a clinically and genetically heterogeneous autosomal recessive disorder with mutations identified in several genes: OCA1 (tyrosinase, TYR), OCA2 (OCA2), OCA3 (tyrosinase-related protein 1, TYRP1), and OCA4 (membrane-associated transporter protein, MATP).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP549973.RAAqw27bvGsiY2ZJ_xQ2_Sb3vkrITS7QzoswPgG2WOjBk130_provenance.
- NP549974.RAA0eXiCE_R6stxF86DVUBcGFO7ZQG0heybTIojTQDOA0130_assertion description "[Non-syndromic oculocutaneous albinism (OCA) is a clinically and genetically heterogeneous autosomal recessive disorder with mutations identified in several genes: OCA1 (tyrosinase, TYR), OCA2 (OCA2), OCA3 (tyrosinase-related protein 1, TYRP1), and OCA4 (membrane-associated transporter protein, MATP).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP549974.RAA0eXiCE_R6stxF86DVUBcGFO7ZQG0heybTIojTQDOA0130_provenance.
- NP549976.RAuZyTsmKU0kUONwZVpM2uPjC38Cj54pbJW1SRw2AR6zw130_assertion description "[Non-syndromic oculocutaneous albinism (OCA) is a clinically and genetically heterogeneous autosomal recessive disorder with mutations identified in several genes: OCA1 (tyrosinase, TYR), OCA2 (OCA2), OCA3 (tyrosinase-related protein 1, TYRP1), and OCA4 (membrane-associated transporter protein, MATP).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP549976.RAuZyTsmKU0kUONwZVpM2uPjC38Cj54pbJW1SRw2AR6zw130_provenance.