Matches in Nanopublications for { <http://rdf.disgenet.org/nanopublications.trig#NP758014.RAjC8q8nQR_iRCMNU1r7SsG9Wx08TZS4F1JO6ED07A-lM130_assertion> ?p ?o ?g. }
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- NP758014.RAjC8q8nQR_iRCMNU1r7SsG9Wx08TZS4F1JO6ED07A-lM130_assertion type Assertion NP758014.RAjC8q8nQR_iRCMNU1r7SsG9Wx08TZS4F1JO6ED07A-lM130_head.
- NP758014.RAjC8q8nQR_iRCMNU1r7SsG9Wx08TZS4F1JO6ED07A-lM130_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." NP758014.RAjC8q8nQR_iRCMNU1r7SsG9Wx08TZS4F1JO6ED07A-lM130_provenance.
- NP758014.RAjC8q8nQR_iRCMNU1r7SsG9Wx08TZS4F1JO6ED07A-lM130_assertion evidence source_evidence_literature NP758014.RAjC8q8nQR_iRCMNU1r7SsG9Wx08TZS4F1JO6ED07A-lM130_provenance.
- NP758014.RAjC8q8nQR_iRCMNU1r7SsG9Wx08TZS4F1JO6ED07A-lM130_assertion SIO_000772 15459825 NP758014.RAjC8q8nQR_iRCMNU1r7SsG9Wx08TZS4F1JO6ED07A-lM130_provenance.
- NP758014.RAjC8q8nQR_iRCMNU1r7SsG9Wx08TZS4F1JO6ED07A-lM130_assertion wasDerivedFrom befree-20140225 NP758014.RAjC8q8nQR_iRCMNU1r7SsG9Wx08TZS4F1JO6ED07A-lM130_provenance.
- NP758014.RAjC8q8nQR_iRCMNU1r7SsG9Wx08TZS4F1JO6ED07A-lM130_assertion wasGeneratedBy ECO_0000203 NP758014.RAjC8q8nQR_iRCMNU1r7SsG9Wx08TZS4F1JO6ED07A-lM130_provenance.