Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP462805.RAcRa5BQHQHQlBv3nlKW_36yGGVer5HMy2zPo0CEKJzEM130_assertion> ?p ?o ?g. }
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- NP462805.RAcRa5BQHQHQlBv3nlKW_36yGGVer5HMy2zPo0CEKJzEM130_assertion type Assertion NP462805.RAcRa5BQHQHQlBv3nlKW_36yGGVer5HMy2zPo0CEKJzEM130_head.
- NP462805.RAcRa5BQHQHQlBv3nlKW_36yGGVer5HMy2zPo0CEKJzEM130_assertion description "[In over 50% of cases the causative gene is CACNA1A (FHM1), which in some cases produces a phenotype with cerebellar signs, including ataxia and nystagmus.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP462805.RAcRa5BQHQHQlBv3nlKW_36yGGVer5HMy2zPo0CEKJzEM130_provenance.
- NP462805.RAcRa5BQHQHQlBv3nlKW_36yGGVer5HMy2zPo0CEKJzEM130_assertion evidence source_evidence_literature NP462805.RAcRa5BQHQHQlBv3nlKW_36yGGVer5HMy2zPo0CEKJzEM130_provenance.
- NP462805.RAcRa5BQHQHQlBv3nlKW_36yGGVer5HMy2zPo0CEKJzEM130_assertion SIO_000772 15459825 NP462805.RAcRa5BQHQHQlBv3nlKW_36yGGVer5HMy2zPo0CEKJzEM130_provenance.
- NP462805.RAcRa5BQHQHQlBv3nlKW_36yGGVer5HMy2zPo0CEKJzEM130_assertion wasDerivedFrom befree-2016 NP462805.RAcRa5BQHQHQlBv3nlKW_36yGGVer5HMy2zPo0CEKJzEM130_provenance.
- NP462805.RAcRa5BQHQHQlBv3nlKW_36yGGVer5HMy2zPo0CEKJzEM130_assertion wasGeneratedBy ECO_0000203 NP462805.RAcRa5BQHQHQlBv3nlKW_36yGGVer5HMy2zPo0CEKJzEM130_provenance.