Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP1326765.RAjVZwWFiXhcNEqBBGJHa4eMPXLI3-Trz5fzxxSL5VmCE#assertion> ?p ?o ?g. }
Showing items 1 to 5 of
5
with 100 items per page.
- assertion description "[2 patients whose clinical features resembled those of multiple system atrophy of the cerebellar subtype (MSA-C) but without ocular motor apraxia and hypoalbuminemia/had a different nucleotide transition in the APTX gene.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.
- assertion evidence source_evidence_literature provenance.
- assertion SIO_000772 17049295 provenance.
- assertion wasDerivedFrom LHGDN provenance.
- assertion wasGeneratedBy ECO_0000203 provenance.