Matches in Nanopublications for { ?s ?p "[Spastic paraplegia type 4 (SPG4) is the most common autosomal dominant hereditary SPG caused by mutations in the SPAST gene.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine."@en ?g. }
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- NP193412.RARF-jhM9-pA8rcgNgZ2wx3JUItDzwd-gBQP8YwvYpZ2w130_assertion description "[Spastic paraplegia type 4 (SPG4) is the most common autosomal dominant hereditary SPG caused by mutations in the SPAST gene.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP193412.RARF-jhM9-pA8rcgNgZ2wx3JUItDzwd-gBQP8YwvYpZ2w130_provenance.
- NP426399.RA-d87ezaLXN_Mc7nib7iAZoIT1wTmg6PEmoS6ZyFvFR4130_assertion description "[Spastic paraplegia type 4 (SPG4) is the most common autosomal dominant hereditary SPG caused by mutations in the SPAST gene.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP426399.RA-d87ezaLXN_Mc7nib7iAZoIT1wTmg6PEmoS6ZyFvFR4130_provenance.
- NP713922.RAUUVWtEMqAoIewYPRtZIUx-u2GVMOeBjqeneKcatiTUA130_assertion description "[Spastic paraplegia type 4 (SPG4) is the most common autosomal dominant hereditary SPG caused by mutations in the SPAST gene.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP713922.RAUUVWtEMqAoIewYPRtZIUx-u2GVMOeBjqeneKcatiTUA130_provenance.
- NP920881.RAZf2IKV0sn0nle-n7573Vm0LCW1WQBp5vqVfpf5RzxGw130_assertion description "[Spastic paraplegia type 4 (SPG4) is the most common autosomal dominant hereditary SPG caused by mutations in the SPAST gene.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP920881.RAZf2IKV0sn0nle-n7573Vm0LCW1WQBp5vqVfpf5RzxGw130_provenance.
- assertion description "[Spastic paraplegia type 4 (SPG4) is the most common autosomal dominant hereditary SPG caused by mutations in the SPAST gene.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.
- assertion description "[Spastic paraplegia type 4 (SPG4) is the most common autosomal dominant hereditary SPG caused by mutations in the SPAST gene.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.
- assertion description "[Spastic paraplegia type 4 (SPG4) is the most common autosomal dominant hereditary SPG caused by mutations in the SPAST gene.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.
- assertion description "[Spastic paraplegia type 4 (SPG4) is the most common autosomal dominant hereditary SPG caused by mutations in the SPAST gene.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.
- assertion description "[Spastic paraplegia type 4 (SPG4) is the most common autosomal dominant hereditary SPG caused by mutations in the SPAST gene.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.
- NP840720.RAYpQKiwPmw7s_7pv3zn3IeLmau9Glmzim_bJaw6WVVxo130_assertion description "[Spastic paraplegia type 4 (SPG4) is the most common autosomal dominant hereditary SPG caused by mutations in the SPAST gene.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP840720.RAYpQKiwPmw7s_7pv3zn3IeLmau9Glmzim_bJaw6WVVxo130_provenance.
- NP933194.RA4lI-jpFy49236m3vGjMhFakSnBwAnKnZu3o6O5B7TBU130_assertion description "[Spastic paraplegia type 4 (SPG4) is the most common autosomal dominant hereditary SPG caused by mutations in the SPAST gene.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP933194.RA4lI-jpFy49236m3vGjMhFakSnBwAnKnZu3o6O5B7TBU130_provenance.
- NP840721.RA3J7PJTLiGSyLOCFfxIhQb0XpXBlKX1vjNkfNz8KCJgE130_assertion description "[Spastic paraplegia type 4 (SPG4) is the most common autosomal dominant hereditary SPG caused by mutations in the SPAST gene.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP840721.RA3J7PJTLiGSyLOCFfxIhQb0XpXBlKX1vjNkfNz8KCJgE130_provenance.