Matches in Nanopublications for { ?s ?p "[New molecular mechanism for Ullrich congenital muscular dystrophy: a heterozygous in-frame deletion in the COL6A1 gene causes a severe phenotype.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine."@en ?g. }
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- NP46655.RARv2SvWBO33dt6Y0uAAZPwj3prrfPLPjKSNtKe-TMzSU130_assertion description "[New molecular mechanism for Ullrich congenital muscular dystrophy: a heterozygous in-frame deletion in the COL6A1 gene causes a severe phenotype.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP46655.RARv2SvWBO33dt6Y0uAAZPwj3prrfPLPjKSNtKe-TMzSU130_provenance.
- NP345017.RA8rIKJdpN7O68LZl13htTTBeH6_xLbstYfVNEaZueJJs130_assertion description "[New molecular mechanism for Ullrich congenital muscular dystrophy: a heterozygous in-frame deletion in the COL6A1 gene causes a severe phenotype.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP345017.RA8rIKJdpN7O68LZl13htTTBeH6_xLbstYfVNEaZueJJs130_provenance.
- NP56323.RAZ1rtGODxO79g9nbAsWCbL7M4UxXMzlCD1RM3o1Rs2mM130_assertion description "[New molecular mechanism for Ullrich congenital muscular dystrophy: a heterozygous in-frame deletion in the COL6A1 gene causes a severe phenotype.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP56323.RAZ1rtGODxO79g9nbAsWCbL7M4UxXMzlCD1RM3o1Rs2mM130_provenance.
- assertion description "[New molecular mechanism for Ullrich congenital muscular dystrophy: a heterozygous in-frame deletion in the COL6A1 gene causes a severe phenotype.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.
- assertion description "[New molecular mechanism for Ullrich congenital muscular dystrophy: a heterozygous in-frame deletion in the COL6A1 gene causes a severe phenotype.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.
- NP400422.RAWgdrUF3v0Ygn8Nsmo0EyvW_BamMnzGGa6xXevFWR8lM130_assertion description "[New molecular mechanism for Ullrich congenital muscular dystrophy: a heterozygous in-frame deletion in the COL6A1 gene causes a severe phenotype.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP400422.RAWgdrUF3v0Ygn8Nsmo0EyvW_BamMnzGGa6xXevFWR8lM130_provenance.
- NP80488.RA6YDq7NbOUXzabp7BrXP7ZXH-qojsFhirDf6HyCvWWYA130_assertion description "[New molecular mechanism for Ullrich congenital muscular dystrophy: a heterozygous in-frame deletion in the COL6A1 gene causes a severe phenotype.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP80488.RA6YDq7NbOUXzabp7BrXP7ZXH-qojsFhirDf6HyCvWWYA130_provenance.