Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP1327905.RAgPAXTs27DHhLnqLHWHy68iSey7xwySWHO8z46yJZaFo#assertion> ?p ?o ?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.
- assertion evidence source_evidence_literature provenance.
- assertion SIO_000772 25652355 provenance.
- assertion wasDerivedFrom BEFREE provenance.
- assertion wasGeneratedBy ECO_0000203 provenance.