Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP257187.RApNe_fFX178pRxD_xsRIxWxKIC0DxEcO-8OzRlGHioWg130_assertion> ?p ?o ?g. }
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- NP257187.RApNe_fFX178pRxD_xsRIxWxKIC0DxEcO-8OzRlGHioWg130_assertion type Assertion NP257187.RApNe_fFX178pRxD_xsRIxWxKIC0DxEcO-8OzRlGHioWg130_head.
- NP257187.RApNe_fFX178pRxD_xsRIxWxKIC0DxEcO-8OzRlGHioWg130_assertion wasGeneratedBy ECO_0000203 NP257187.RApNe_fFX178pRxD_xsRIxWxKIC0DxEcO-8OzRlGHioWg130_provenance.
- NP257187.RApNe_fFX178pRxD_xsRIxWxKIC0DxEcO-8OzRlGHioWg130_assertion wasDerivedFrom befree-2016 NP257187.RApNe_fFX178pRxD_xsRIxWxKIC0DxEcO-8OzRlGHioWg130_provenance.
- NP257187.RApNe_fFX178pRxD_xsRIxWxKIC0DxEcO-8OzRlGHioWg130_assertion SIO_000772 10399872 NP257187.RApNe_fFX178pRxD_xsRIxWxKIC0DxEcO-8OzRlGHioWg130_provenance.
- NP257187.RApNe_fFX178pRxD_xsRIxWxKIC0DxEcO-8OzRlGHioWg130_assertion evidence source_evidence_literature NP257187.RApNe_fFX178pRxD_xsRIxWxKIC0DxEcO-8OzRlGHioWg130_provenance.
- NP257187.RApNe_fFX178pRxD_xsRIxWxKIC0DxEcO-8OzRlGHioWg130_assertion description "[Clinical and molecular studies of 73 Italian families with autosomal dominant cerebellar ataxia type I: SCA1 and SCA2 are the most common genotypes.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP257187.RApNe_fFX178pRxD_xsRIxWxKIC0DxEcO-8OzRlGHioWg130_provenance.