Matches in Nanopublications for { ?s ?p "[Taken together, TGFB2 is a rarely mutated gene in patients with syndromic TAAD, and the clinical features of our TGFB2 mutation-positive individuals fit in the scheme of LDS, rather than MFS-related disorders.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine."@en ?g. }
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- assertion description "[Taken together, TGFB2 is a rarely mutated gene in patients with syndromic TAAD, and the clinical features of our TGFB2 mutation-positive individuals fit in the scheme of LDS, rather than MFS-related disorders.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.
- assertion description "[Taken together, TGFB2 is a rarely mutated gene in patients with syndromic TAAD, and the clinical features of our TGFB2 mutation-positive individuals fit in the scheme of LDS, rather than MFS-related disorders.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.
- NP733419.RAC-oeN_8c4fKVf-CU_-1wOoAbmL7oPEmez2FshVgcXB4130_assertion description "[Taken together, TGFB2 is a rarely mutated gene in patients with syndromic TAAD, and the clinical features of our TGFB2 mutation-positive individuals fit in the scheme of LDS, rather than MFS-related disorders.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP733419.RAC-oeN_8c4fKVf-CU_-1wOoAbmL7oPEmez2FshVgcXB4130_provenance.
- NP733578.RAp8ikrQXTgM-EZSsusuUWczRWZhRLrNOv1Hy1a9aHmn8130_assertion description "[Taken together, TGFB2 is a rarely mutated gene in patients with syndromic TAAD, and the clinical features of our TGFB2 mutation-positive individuals fit in the scheme of LDS, rather than MFS-related disorders.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP733578.RAp8ikrQXTgM-EZSsusuUWczRWZhRLrNOv1Hy1a9aHmn8130_provenance.
- NP1125192.RAp-KB-39J-K4Nyb3J3JopMmF5FNaaHtlLrIfFttm38Qo130_assertion description "[Taken together, TGFB2 is a rarely mutated gene in patients with syndromic TAAD, and the clinical features of our TGFB2 mutation-positive individuals fit in the scheme of LDS, rather than MFS-related disorders.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1125192.RAp-KB-39J-K4Nyb3J3JopMmF5FNaaHtlLrIfFttm38Qo130_provenance.
- NP1125191.RA8wLrYwImooFZxQa0iVARGLagLhLVZRbpkS1J7NxAWRc130_assertion description "[Taken together, TGFB2 is a rarely mutated gene in patients with syndromic TAAD, and the clinical features of our TGFB2 mutation-positive individuals fit in the scheme of LDS, rather than MFS-related disorders.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1125191.RA8wLrYwImooFZxQa0iVARGLagLhLVZRbpkS1J7NxAWRc130_provenance.