Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP575014.RA7IxjD2MCk7VJynJ2XK_70MQc01eWOksdXSVa7DkE8G8130_assertion> ?p ?o ?g. }
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- NP575014.RA7IxjD2MCk7VJynJ2XK_70MQc01eWOksdXSVa7DkE8G8130_assertion type Assertion NP575014.RA7IxjD2MCk7VJynJ2XK_70MQc01eWOksdXSVa7DkE8G8130_head.
- NP575014.RA7IxjD2MCk7VJynJ2XK_70MQc01eWOksdXSVa7DkE8G8130_assertion description "[We describe 2 patients whose clinical features resembled those of multiple system atrophy of the cerebellar subtype (MSA-C) but without ocular motor apraxia and hypoalbuminemia.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP575014.RA7IxjD2MCk7VJynJ2XK_70MQc01eWOksdXSVa7DkE8G8130_provenance.
- NP575014.RA7IxjD2MCk7VJynJ2XK_70MQc01eWOksdXSVa7DkE8G8130_assertion evidence source_evidence_literature NP575014.RA7IxjD2MCk7VJynJ2XK_70MQc01eWOksdXSVa7DkE8G8130_provenance.
- NP575014.RA7IxjD2MCk7VJynJ2XK_70MQc01eWOksdXSVa7DkE8G8130_assertion SIO_000772 17049295 NP575014.RA7IxjD2MCk7VJynJ2XK_70MQc01eWOksdXSVa7DkE8G8130_provenance.
- NP575014.RA7IxjD2MCk7VJynJ2XK_70MQc01eWOksdXSVa7DkE8G8130_assertion wasDerivedFrom befree-2016 NP575014.RA7IxjD2MCk7VJynJ2XK_70MQc01eWOksdXSVa7DkE8G8130_provenance.
- NP575014.RA7IxjD2MCk7VJynJ2XK_70MQc01eWOksdXSVa7DkE8G8130_assertion wasGeneratedBy ECO_0000203 NP575014.RA7IxjD2MCk7VJynJ2XK_70MQc01eWOksdXSVa7DkE8G8130_provenance.