Matches in Nanopublications for { ?s ?p "[RAG1 Arg972Qln mutation, located in the primary sequence near catalytic amino acid Glu962, is hypersensitive to certain coding flank sequences in a patient with Omenn syndrome.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine."@en ?g. }
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- NP135768.RAzFoXdC9l1agSJl1nHlFMcbU7_t8GKmPfQSy4yc0bmNs130_assertion description "[RAG1 Arg972Qln mutation, located in the primary sequence near catalytic amino acid Glu962, is hypersensitive to certain coding flank sequences in a patient with Omenn syndrome.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP135768.RAzFoXdC9l1agSJl1nHlFMcbU7_t8GKmPfQSy4yc0bmNs130_provenance.
- assertion description "[RAG1 Arg972Qln mutation, located in the primary sequence near catalytic amino acid Glu962, is hypersensitive to certain coding flank sequences in a patient with Omenn syndrome.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.
- NP198923.RAoSSCD8uTObLHpJnuZe-5yTVyJVqDRBhf0rLkd6iGh0g130_assertion description "[RAG1 Arg972Qln mutation, located in the primary sequence near catalytic amino acid Glu962, is hypersensitive to certain coding flank sequences in a patient with Omenn syndrome.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP198923.RAoSSCD8uTObLHpJnuZe-5yTVyJVqDRBhf0rLkd6iGh0g130_provenance.
- NP241673.RAcy6N4qWDDmrYKJ9uQpdGPdSTDeU8VifdWl8wcfPhzRQ130_assertion description "[RAG1 Arg972Qln mutation, located in the primary sequence near catalytic amino acid Glu962, is hypersensitive to certain coding flank sequences in a patient with Omenn syndrome.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP241673.RAcy6N4qWDDmrYKJ9uQpdGPdSTDeU8VifdWl8wcfPhzRQ130_provenance.