Nanopublications LDF server

Matches in Nanopublications for { ?s ?p "[The phenotypes of four allelic mutations identified in the sodium channel gene Scn8a range from ataxia and muscle weakness through severe dystonia and progressive paralysis, indicating that human mutations in this gene could be associated with a variety of clinical syndromes.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine."@en ?g. }

• NP683290.RAeVPe9ASyGwZ8pc-U4s5TVqDNrdbmSo_A9-TzoW6flNk130_assertion description "[The phenotypes of four allelic mutations identified in the sodium channel gene Scn8a range from ataxia and muscle weakness through severe dystonia and progressive paralysis, indicating that human mutations in this gene could be associated with a variety of clinical syndromes.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP683290.RAeVPe9ASyGwZ8pc-U4s5TVqDNrdbmSo_A9-TzoW6flNk130_provenance.
• NP683349.RAW66Qw39xmZEjfa21PDABxuUn_LvlmOAIae_1dYhzrFo130_assertion description "[The phenotypes of four allelic mutations identified in the sodium channel gene Scn8a range from ataxia and muscle weakness through severe dystonia and progressive paralysis, indicating that human mutations in this gene could be associated with a variety of clinical syndromes.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP683349.RAW66Qw39xmZEjfa21PDABxuUn_LvlmOAIae_1dYhzrFo130_provenance.
• assertion description "[The phenotypes of four allelic mutations identified in the sodium channel gene Scn8a range from ataxia and muscle weakness through severe dystonia and progressive paralysis, indicating that human mutations in this gene could be associated with a variety of clinical syndromes.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.
• assertion description "[The phenotypes of four allelic mutations identified in the sodium channel gene Scn8a range from ataxia and muscle weakness through severe dystonia and progressive paralysis, indicating that human mutations in this gene could be associated with a variety of clinical syndromes.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.
• assertion description "[The phenotypes of four allelic mutations identified in the sodium channel gene Scn8a range from ataxia and muscle weakness through severe dystonia and progressive paralysis, indicating that human mutations in this gene could be associated with a variety of clinical syndromes.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.
• assertion description "[The phenotypes of four allelic mutations identified in the sodium channel gene Scn8a range from ataxia and muscle weakness through severe dystonia and progressive paralysis, indicating that human mutations in this gene could be associated with a variety of clinical syndromes.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.
• assertion description "[The phenotypes of four allelic mutations identified in the sodium channel gene Scn8a range from ataxia and muscle weakness through severe dystonia and progressive paralysis, indicating that human mutations in this gene could be associated with a variety of clinical syndromes.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.
• assertion description "[The phenotypes of four allelic mutations identified in the sodium channel gene Scn8a range from ataxia and muscle weakness through severe dystonia and progressive paralysis, indicating that human mutations in this gene could be associated with a variety of clinical syndromes.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.
• assertion description "[The phenotypes of four allelic mutations identified in the sodium channel gene Scn8a range from ataxia and muscle weakness through severe dystonia and progressive paralysis, indicating that human mutations in this gene could be associated with a variety of clinical syndromes.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.
• NP1393862.RAZDfFFlioWqUFAs7ZsYNAsRnwjigXleLWzzoODM_yrtI130_assertion description "[The phenotypes of four allelic mutations identified in the sodium channel gene Scn8a range from ataxia and muscle weakness through severe dystonia and progressive paralysis, indicating that human mutations in this gene could be associated with a variety of clinical syndromes.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1393862.RAZDfFFlioWqUFAs7ZsYNAsRnwjigXleLWzzoODM_yrtI130_provenance.
• NP1393865.RAeOXII3XgVTaT4iKmJhUqmZHeD84IfxBtUSRyjEMTCAo130_assertion description "[The phenotypes of four allelic mutations identified in the sodium channel gene Scn8a range from ataxia and muscle weakness through severe dystonia and progressive paralysis, indicating that human mutations in this gene could be associated with a variety of clinical syndromes.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1393865.RAeOXII3XgVTaT4iKmJhUqmZHeD84IfxBtUSRyjEMTCAo130_provenance.
• NP1393869.RAdxw-bbSVxQ05rvrwBHm_oNIWxFJeQwhNskBWQO9tpzk130_assertion description "[The phenotypes of four allelic mutations identified in the sodium channel gene Scn8a range from ataxia and muscle weakness through severe dystonia and progressive paralysis, indicating that human mutations in this gene could be associated with a variety of clinical syndromes.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1393869.RAdxw-bbSVxQ05rvrwBHm_oNIWxFJeQwhNskBWQO9tpzk130_provenance.
• NP1393870.RAueFWUlEgv_mzL2hl4yOz-OH1OlZ2n0ieTkf9QfcdTDY130_assertion description "[The phenotypes of four allelic mutations identified in the sodium channel gene Scn8a range from ataxia and muscle weakness through severe dystonia and progressive paralysis, indicating that human mutations in this gene could be associated with a variety of clinical syndromes.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1393870.RAueFWUlEgv_mzL2hl4yOz-OH1OlZ2n0ieTkf9QfcdTDY130_provenance.
• NP683346.RANVikJ_a_8qD-2Y3KD4AB3lmGPNycMq1yp9MNsQtWN60130_assertion description "[The phenotypes of four allelic mutations identified in the sodium channel gene Scn8a range from ataxia and muscle weakness through severe dystonia and progressive paralysis, indicating that human mutations in this gene could be associated with a variety of clinical syndromes.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP683346.RANVikJ_a_8qD-2Y3KD4AB3lmGPNycMq1yp9MNsQtWN60130_provenance.
• NP683358.RAIYLYX8bGzfb1WvERF4EIVvFm9OY1_mMsROYGq_8CBTE130_assertion description "[The phenotypes of four allelic mutations identified in the sodium channel gene Scn8a range from ataxia and muscle weakness through severe dystonia and progressive paralysis, indicating that human mutations in this gene could be associated with a variety of clinical syndromes.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP683358.RAIYLYX8bGzfb1WvERF4EIVvFm9OY1_mMsROYGq_8CBTE130_provenance.
• NP1393866.RAPQ2TQ8F1DkzeUnkm1u8ct8UCw0Z2GmRo2vH0OGPPuDw130_assertion description "[The phenotypes of four allelic mutations identified in the sodium channel gene Scn8a range from ataxia and muscle weakness through severe dystonia and progressive paralysis, indicating that human mutations in this gene could be associated with a variety of clinical syndromes.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1393866.RAPQ2TQ8F1DkzeUnkm1u8ct8UCw0Z2GmRo2vH0OGPPuDw130_provenance.
• NP683282.RA39JdOqcP2srox4on_LKCJHendXCxh3KeiQqJfd7jeF0130_assertion description "[The phenotypes of four allelic mutations identified in the sodium channel gene Scn8a range from ataxia and muscle weakness through severe dystonia and progressive paralysis, indicating that human mutations in this gene could be associated with a variety of clinical syndromes.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP683282.RA39JdOqcP2srox4on_LKCJHendXCxh3KeiQqJfd7jeF0130_provenance.
• NP683333.RA3KsQHhf3zRHg7dxYWR7wC96Y2PSDbj7R3T7pvJt03_0130_assertion description "[The phenotypes of four allelic mutations identified in the sodium channel gene Scn8a range from ataxia and muscle weakness through severe dystonia and progressive paralysis, indicating that human mutations in this gene could be associated with a variety of clinical syndromes.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP683333.RA3KsQHhf3zRHg7dxYWR7wC96Y2PSDbj7R3T7pvJt03_0130_provenance.
• NP1393867.RA5LPS-4w6pitcToNTvvvMoqk4KfiV9owHHOxWi1aGOP4130_assertion description "[The phenotypes of four allelic mutations identified in the sodium channel gene Scn8a range from ataxia and muscle weakness through severe dystonia and progressive paralysis, indicating that human mutations in this gene could be associated with a variety of clinical syndromes.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1393867.RA5LPS-4w6pitcToNTvvvMoqk4KfiV9owHHOxWi1aGOP4130_provenance.