Matches in Nanopublications for { ?s ?p "[This model, where dominant mutations cause mild Bethlem myopathy and recessive mutations cause severe UCMD was recently challenged when a patient with UCMD was shown to have a heterozygous in-frame deletion in COL6A1.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine."@en ?g. }
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- NP320342.RAdi59Q2vdrcsNPmVOk6SpThjEDXj06_iBR1_5br-QnSw130_assertion description "[This model, where dominant mutations cause mild Bethlem myopathy and recessive mutations cause severe UCMD was recently challenged when a patient with UCMD was shown to have a heterozygous in-frame deletion in COL6A1.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP320342.RAdi59Q2vdrcsNPmVOk6SpThjEDXj06_iBR1_5br-QnSw130_provenance.
- assertion description "[This model, where dominant mutations cause mild Bethlem myopathy and recessive mutations cause severe UCMD was recently challenged when a patient with UCMD was shown to have a heterozygous in-frame deletion in COL6A1.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.
- assertion description "[This model, where dominant mutations cause mild Bethlem myopathy and recessive mutations cause severe UCMD was recently challenged when a patient with UCMD was shown to have a heterozygous in-frame deletion in COL6A1.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.
- NP470131.RAFW9AvYgW_Eh5cWVgdL-6bTxmsL7orrK8BUNC4xggWA4130_assertion description "[This model, where dominant mutations cause mild Bethlem myopathy and recessive mutations cause severe UCMD was recently challenged when a patient with UCMD was shown to have a heterozygous in-frame deletion in COL6A1.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP470131.RAFW9AvYgW_Eh5cWVgdL-6bTxmsL7orrK8BUNC4xggWA4130_provenance.
- NP470134.RAvY4G-eWcLSguSecIb2-oBlwl8UsX6rl1UGKEoT9lhuU130_assertion description "[This model, where dominant mutations cause mild Bethlem myopathy and recessive mutations cause severe UCMD was recently challenged when a patient with UCMD was shown to have a heterozygous in-frame deletion in COL6A1.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP470134.RAvY4G-eWcLSguSecIb2-oBlwl8UsX6rl1UGKEoT9lhuU130_provenance.