Matches in Nanopublications for { ?s ?p "[A missense mutation in SLC33A1, which encodes the acetyl-CoA transporter, causes autosomal-dominant spastic paraplegia (SPG42).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine."@en ?g. }
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- NP613158.RABxsoO6TmPJ8WPmATKh7nJvU0P2QUf-wqGc79s3fFbsg130_assertion description "[A missense mutation in SLC33A1, which encodes the acetyl-CoA transporter, causes autosomal-dominant spastic paraplegia (SPG42).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP613158.RABxsoO6TmPJ8WPmATKh7nJvU0P2QUf-wqGc79s3fFbsg130_provenance.
- NP6119.RA4EAJDZApbrR-Pypyq0ApXR6RcNXD7TeNCmmYmICHl70130_assertion description "[A missense mutation in SLC33A1, which encodes the acetyl-CoA transporter, causes autosomal-dominant spastic paraplegia (SPG42).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP6119.RA4EAJDZApbrR-Pypyq0ApXR6RcNXD7TeNCmmYmICHl70130_provenance.
- NP880211.RAxVaWkf9j159yAUsKKklDtSgdB-PSx4K5kV5YI-xuJps130_assertion description "[A missense mutation in SLC33A1, which encodes the acetyl-CoA transporter, causes autosomal-dominant spastic paraplegia (SPG42).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP880211.RAxVaWkf9j159yAUsKKklDtSgdB-PSx4K5kV5YI-xuJps130_provenance.
- NP5602.RAcD7xDaFxKVGCiRzB_nDukTQxSbBw7r8hdnhREtvnG8Y130_assertion description "[A missense mutation in SLC33A1, which encodes the acetyl-CoA transporter, causes autosomal-dominant spastic paraplegia (SPG42).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP5602.RAcD7xDaFxKVGCiRzB_nDukTQxSbBw7r8hdnhREtvnG8Y130_provenance.
- assertion description "[A missense mutation in SLC33A1, which encodes the acetyl-CoA transporter, causes autosomal-dominant spastic paraplegia (SPG42).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.
- assertion description "[A missense mutation in SLC33A1, which encodes the acetyl-CoA transporter, causes autosomal-dominant spastic paraplegia (SPG42).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.
- assertion description "[A missense mutation in SLC33A1, which encodes the acetyl-CoA transporter, causes autosomal-dominant spastic paraplegia (SPG42).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.
- NP817317.RA-6DGMCCzGMJfeS26bpHLc3OP0tuGt2Yxaj6BsqVXt9w130_assertion description "[A missense mutation in SLC33A1, which encodes the acetyl-CoA transporter, causes autosomal-dominant spastic paraplegia (SPG42).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP817317.RA-6DGMCCzGMJfeS26bpHLc3OP0tuGt2Yxaj6BsqVXt9w130_provenance.
- NP707724.RAHi3sSLruhdP49xN9O9O712seL8m8ikvGWwpG1vM3W1I130_assertion description "[A missense mutation in SLC33A1, which encodes the acetyl-CoA transporter, causes autosomal-dominant spastic paraplegia (SPG42).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP707724.RAHi3sSLruhdP49xN9O9O712seL8m8ikvGWwpG1vM3W1I130_provenance.