Matches in Nanopublications for { ?s ?p "[Autosomal recessive mutations in the ALS2 gene have been linked to juvenile-onset amyotrophic lateral sclerosis (ALS2), primary lateral sclerosis and juvenile-onset ascending hereditary spastic paraplegia.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine."@en ?g. }
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- NP487470.RAwrc13GiX0T_fzDP9CdlCYny3FZ2Jv-Ai0kLZfzjeWJM130_assertion description "[Autosomal recessive mutations in the ALS2 gene have been linked to juvenile-onset amyotrophic lateral sclerosis (ALS2), primary lateral sclerosis and juvenile-onset ascending hereditary spastic paraplegia.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP487470.RAwrc13GiX0T_fzDP9CdlCYny3FZ2Jv-Ai0kLZfzjeWJM130_provenance.
- NP794392.RAZSByKIZuOKi7aU3_l_AjMVxKYh92gEn-geTtKL4rlsU130_assertion description "[Autosomal recessive mutations in the ALS2 gene have been linked to juvenile-onset amyotrophic lateral sclerosis (ALS2), primary lateral sclerosis and juvenile-onset ascending hereditary spastic paraplegia.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP794392.RAZSByKIZuOKi7aU3_l_AjMVxKYh92gEn-geTtKL4rlsU130_provenance.
- NP455003.RA9jvBoK0LbCAoNmMbo-MfXkzaqOkxJJ8HaarGN23S_Cs130_assertion description "[Autosomal recessive mutations in the ALS2 gene have been linked to juvenile-onset amyotrophic lateral sclerosis (ALS2), primary lateral sclerosis and juvenile-onset ascending hereditary spastic paraplegia.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP455003.RA9jvBoK0LbCAoNmMbo-MfXkzaqOkxJJ8HaarGN23S_Cs130_provenance.
- NP932821.RATY8XlFlm8eBFsEP0MIPrkzwvgREvHZACHzv61Oy2gME130_assertion description "[Autosomal recessive mutations in the ALS2 gene have been linked to juvenile-onset amyotrophic lateral sclerosis (ALS2), primary lateral sclerosis and juvenile-onset ascending hereditary spastic paraplegia.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP932821.RATY8XlFlm8eBFsEP0MIPrkzwvgREvHZACHzv61Oy2gME130_provenance.
- assertion description "[Autosomal recessive mutations in the ALS2 gene have been linked to juvenile-onset amyotrophic lateral sclerosis (ALS2), primary lateral sclerosis and juvenile-onset ascending hereditary spastic paraplegia.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.
- assertion description "[Autosomal recessive mutations in the ALS2 gene have been linked to juvenile-onset amyotrophic lateral sclerosis (ALS2), primary lateral sclerosis and juvenile-onset ascending hereditary spastic paraplegia.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.
- NP688598.RAMbgWJC_br8shPH4_qa0IuiwDxkUmGMRJDzOsXraLMyc130_assertion description "[Autosomal recessive mutations in the ALS2 gene have been linked to juvenile-onset amyotrophic lateral sclerosis (ALS2), primary lateral sclerosis and juvenile-onset ascending hereditary spastic paraplegia.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP688598.RAMbgWJC_br8shPH4_qa0IuiwDxkUmGMRJDzOsXraLMyc130_provenance.
- NP932810.RAyBPILfUa0sPJUN2cTOMoqbz4Y0NO8L6H9sA2-KgWEh4130_assertion description "[Autosomal recessive mutations in the ALS2 gene have been linked to juvenile-onset amyotrophic lateral sclerosis (ALS2), primary lateral sclerosis and juvenile-onset ascending hereditary spastic paraplegia.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP932810.RAyBPILfUa0sPJUN2cTOMoqbz4Y0NO8L6H9sA2-KgWEh4130_provenance.
- NP688600.RA3hOmocQkfZkE55Kby_SJUAOcfdc4IGA3ApqLubA467Y130_assertion description "[Autosomal recessive mutations in the ALS2 gene have been linked to juvenile-onset amyotrophic lateral sclerosis (ALS2), primary lateral sclerosis and juvenile-onset ascending hereditary spastic paraplegia.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP688600.RA3hOmocQkfZkE55Kby_SJUAOcfdc4IGA3ApqLubA467Y130_provenance.