Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP1362929.RAf4VxqCRPY4QfxHvqWb73CR0QIfGZtIzhnOw_oi41cfw130_assertion> ?p ?o ?g. }
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- NP1362929.RAf4VxqCRPY4QfxHvqWb73CR0QIfGZtIzhnOw_oi41cfw130_assertion type Assertion NP1362929.RAf4VxqCRPY4QfxHvqWb73CR0QIfGZtIzhnOw_oi41cfw130_head.
- NP1362929.RAf4VxqCRPY4QfxHvqWb73CR0QIfGZtIzhnOw_oi41cfw130_assertion description "[Sixty-five patients suffering from autosomal dominant cerebellar ataxia-I(ADCA-1) were subjected genotype phenotype correlation analysis using molecular genetic assignment to the spinocerebellar ataxia type 1, 2 or 3 (SCA1, -2 or -3) locus, clinical examination, eye movement recording and morphometric analysis of MRIs.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1362929.RAf4VxqCRPY4QfxHvqWb73CR0QIfGZtIzhnOw_oi41cfw130_provenance.
- NP1362929.RAf4VxqCRPY4QfxHvqWb73CR0QIfGZtIzhnOw_oi41cfw130_assertion evidence source_evidence_literature NP1362929.RAf4VxqCRPY4QfxHvqWb73CR0QIfGZtIzhnOw_oi41cfw130_provenance.
- NP1362929.RAf4VxqCRPY4QfxHvqWb73CR0QIfGZtIzhnOw_oi41cfw130_assertion SIO_000772 8931575 NP1362929.RAf4VxqCRPY4QfxHvqWb73CR0QIfGZtIzhnOw_oi41cfw130_provenance.
- NP1362929.RAf4VxqCRPY4QfxHvqWb73CR0QIfGZtIzhnOw_oi41cfw130_assertion wasDerivedFrom befree-2016 NP1362929.RAf4VxqCRPY4QfxHvqWb73CR0QIfGZtIzhnOw_oi41cfw130_provenance.
- NP1362929.RAf4VxqCRPY4QfxHvqWb73CR0QIfGZtIzhnOw_oi41cfw130_assertion wasGeneratedBy ECO_0000203 NP1362929.RAf4VxqCRPY4QfxHvqWb73CR0QIfGZtIzhnOw_oi41cfw130_provenance.