Matches in Nanopublications for { ?s ?p "[Mutations in DYNC1H1 are associated with spinal muscular atrophy (SMA), hereditary motor and sensory neuropathy (HMSN), cortical malformations, or a combination of these.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine."@en ?g. }
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- assertion description "[Mutations in DYNC1H1 are associated with spinal muscular atrophy (SMA), hereditary motor and sensory neuropathy (HMSN), cortical malformations, or a combination of these.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.
- assertion description "[Mutations in DYNC1H1 are associated with spinal muscular atrophy (SMA), hereditary motor and sensory neuropathy (HMSN), cortical malformations, or a combination of these.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.
- NP1248403.RAkQIbpv1HLbkBIFmdmo2K35qxCy_TCLqMLBdgzKHisKA130_assertion description "[Mutations in DYNC1H1 are associated with spinal muscular atrophy (SMA), hereditary motor and sensory neuropathy (HMSN), cortical malformations, or a combination of these.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1248403.RAkQIbpv1HLbkBIFmdmo2K35qxCy_TCLqMLBdgzKHisKA130_provenance.
- NP1248405.RAk8iX3gr0fR-1GM4WtYYb27TXl4_KPqUD8sgbGYuac1c130_assertion description "[Mutations in DYNC1H1 are associated with spinal muscular atrophy (SMA), hereditary motor and sensory neuropathy (HMSN), cortical malformations, or a combination of these.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1248405.RAk8iX3gr0fR-1GM4WtYYb27TXl4_KPqUD8sgbGYuac1c130_provenance.