Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP756861.RAHMoM_LzD8pdUOgdp0kILdpKiFxpj9MKnb5P1LKH82D0130_assertion> ?p ?o ?g. }
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- NP756861.RAHMoM_LzD8pdUOgdp0kILdpKiFxpj9MKnb5P1LKH82D0130_assertion type Assertion NP756861.RAHMoM_LzD8pdUOgdp0kILdpKiFxpj9MKnb5P1LKH82D0130_head.
- NP756861.RAHMoM_LzD8pdUOgdp0kILdpKiFxpj9MKnb5P1LKH82D0130_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." NP756861.RAHMoM_LzD8pdUOgdp0kILdpKiFxpj9MKnb5P1LKH82D0130_provenance.
- NP756861.RAHMoM_LzD8pdUOgdp0kILdpKiFxpj9MKnb5P1LKH82D0130_assertion evidence source_evidence_literature NP756861.RAHMoM_LzD8pdUOgdp0kILdpKiFxpj9MKnb5P1LKH82D0130_provenance.
- NP756861.RAHMoM_LzD8pdUOgdp0kILdpKiFxpj9MKnb5P1LKH82D0130_assertion SIO_000772 17049295 NP756861.RAHMoM_LzD8pdUOgdp0kILdpKiFxpj9MKnb5P1LKH82D0130_provenance.
- NP756861.RAHMoM_LzD8pdUOgdp0kILdpKiFxpj9MKnb5P1LKH82D0130_assertion wasDerivedFrom befree-20150227 NP756861.RAHMoM_LzD8pdUOgdp0kILdpKiFxpj9MKnb5P1LKH82D0130_provenance.
- NP756861.RAHMoM_LzD8pdUOgdp0kILdpKiFxpj9MKnb5P1LKH82D0130_assertion wasGeneratedBy ECO_0000203 NP756861.RAHMoM_LzD8pdUOgdp0kILdpKiFxpj9MKnb5P1LKH82D0130_provenance.