Matches in Nanopublications for { <http://rdf.disgenet.org/nanopublications.trig#NP486069.RAtc7xiRqVBF8Xq5pBBcCTuudgnKo9p6yU99xen3fxfYg130_assertion> ?p ?o ?g. }
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- NP486069.RAtc7xiRqVBF8Xq5pBBcCTuudgnKo9p6yU99xen3fxfYg130_assertion type Assertion NP486069.RAtc7xiRqVBF8Xq5pBBcCTuudgnKo9p6yU99xen3fxfYg130_head.
- NP486069.RAtc7xiRqVBF8Xq5pBBcCTuudgnKo9p6yU99xen3fxfYg130_assertion description "[The most common cause of inherited SCA was a mutation at the SCA6 locus (25%), followed by mutation at the SCA1 locus (15%), SCA3 locus (5%) and dentatorubral-pallidoluysian atrophy locus (5%).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP486069.RAtc7xiRqVBF8Xq5pBBcCTuudgnKo9p6yU99xen3fxfYg130_provenance.
- NP486069.RAtc7xiRqVBF8Xq5pBBcCTuudgnKo9p6yU99xen3fxfYg130_assertion evidence source_evidence_literature NP486069.RAtc7xiRqVBF8Xq5pBBcCTuudgnKo9p6yU99xen3fxfYg130_provenance.
- NP486069.RAtc7xiRqVBF8Xq5pBBcCTuudgnKo9p6yU99xen3fxfYg130_assertion SIO_000772 11359084 NP486069.RAtc7xiRqVBF8Xq5pBBcCTuudgnKo9p6yU99xen3fxfYg130_provenance.
- NP486069.RAtc7xiRqVBF8Xq5pBBcCTuudgnKo9p6yU99xen3fxfYg130_assertion wasDerivedFrom befree-20140225 NP486069.RAtc7xiRqVBF8Xq5pBBcCTuudgnKo9p6yU99xen3fxfYg130_provenance.
- NP486069.RAtc7xiRqVBF8Xq5pBBcCTuudgnKo9p6yU99xen3fxfYg130_assertion wasGeneratedBy ECO_0000203 NP486069.RAtc7xiRqVBF8Xq5pBBcCTuudgnKo9p6yU99xen3fxfYg130_provenance.