Matches in Nanopublications for { ?s ?p "[TTC19 mutations constitute a rare cause of CIII deficiency and are associated with neurological disorders in childhood and adulthood.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine."@en ?g. }
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- assertion description "[TTC19 mutations constitute a rare cause of CIII deficiency and are associated with neurological disorders in childhood and adulthood.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.
- NP1261057.RAO93fP87GP1pNxzitiuFKevLKEcfVYjYsRcKUG3f7FVc130_assertion description "[TTC19 mutations constitute a rare cause of CIII deficiency and are associated with neurological disorders in childhood and adulthood.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1261057.RAO93fP87GP1pNxzitiuFKevLKEcfVYjYsRcKUG3f7FVc130_provenance.