Matches in Nanopublications for { ?s ?p "[The novel mutation p.G315X in the OA1 gene was identified in a Chinese family with ocular albinism, which is predicted to generate a premature stop codon.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine."@en ?g. }
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- NP167941.RAhFo5enGIN-dc9dSTqKNxgVSNmTpLxAIXvB_fQldTlP8130_assertion description "[The novel mutation p.G315X in the OA1 gene was identified in a Chinese family with ocular albinism, which is predicted to generate a premature stop codon.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP167941.RAhFo5enGIN-dc9dSTqKNxgVSNmTpLxAIXvB_fQldTlP8130_provenance.
- NP1002281.RAUfP13MnFotR-c_QuIb2YG5aZy14-NalCRqW5AidPUVI130_assertion description "[The novel mutation p.G315X in the OA1 gene was identified in a Chinese family with ocular albinism, which is predicted to generate a premature stop codon.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1002281.RAUfP13MnFotR-c_QuIb2YG5aZy14-NalCRqW5AidPUVI130_provenance.
- NP601241.RApyo7NYBaHoqxXzocXLqEE7bwyHbAx-zMSvp36HbTV-Y130_assertion description "[The novel mutation p.G315X in the OA1 gene was identified in a Chinese family with ocular albinism, which is predicted to generate a premature stop codon.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP601241.RApyo7NYBaHoqxXzocXLqEE7bwyHbAx-zMSvp36HbTV-Y130_provenance.
- NP821212.RAMNbIfz8H6R1bWGQbKJAB8grq3lm_Ff6H0QgJfnjQysY130_assertion description "[The novel mutation p.G315X in the OA1 gene was identified in a Chinese family with ocular albinism, which is predicted to generate a premature stop codon.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP821212.RAMNbIfz8H6R1bWGQbKJAB8grq3lm_Ff6H0QgJfnjQysY130_provenance.
- NP712312.RAd81lgFHogYq0ZvFV7-cVk3a6BYA8OqZBb81A2ZEfqkc130_assertion description "[The novel mutation p.G315X in the OA1 gene was identified in a Chinese family with ocular albinism, which is predicted to generate a premature stop codon.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP712312.RAd81lgFHogYq0ZvFV7-cVk3a6BYA8OqZBb81A2ZEfqkc130_provenance.
- NP712313.RAU_h5oVfNHiOl1m-MAOtiRx8Ne1sfZWHjGsNkxtuUafg130_assertion description "[The novel mutation p.G315X in the OA1 gene was identified in a Chinese family with ocular albinism, which is predicted to generate a premature stop codon.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP712313.RAU_h5oVfNHiOl1m-MAOtiRx8Ne1sfZWHjGsNkxtuUafg130_provenance.