Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP541605.RAjRTB3qC1IUYgpf5av0lWG-gdlqSeC5ekLx2zxgx6DpE130_assertion> ?p ?o ?g. }
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- NP541605.RAjRTB3qC1IUYgpf5av0lWG-gdlqSeC5ekLx2zxgx6DpE130_assertion type Assertion NP541605.RAjRTB3qC1IUYgpf5av0lWG-gdlqSeC5ekLx2zxgx6DpE130_head.
- NP541605.RAjRTB3qC1IUYgpf5av0lWG-gdlqSeC5ekLx2zxgx6DpE130_assertion wasGeneratedBy ECO_0000203 NP541605.RAjRTB3qC1IUYgpf5av0lWG-gdlqSeC5ekLx2zxgx6DpE130_provenance.
- NP541605.RAjRTB3qC1IUYgpf5av0lWG-gdlqSeC5ekLx2zxgx6DpE130_assertion wasDerivedFrom befree-20150227 NP541605.RAjRTB3qC1IUYgpf5av0lWG-gdlqSeC5ekLx2zxgx6DpE130_provenance.
- NP541605.RAjRTB3qC1IUYgpf5av0lWG-gdlqSeC5ekLx2zxgx6DpE130_assertion SIO_000772 10399872 NP541605.RAjRTB3qC1IUYgpf5av0lWG-gdlqSeC5ekLx2zxgx6DpE130_provenance.
- NP541605.RAjRTB3qC1IUYgpf5av0lWG-gdlqSeC5ekLx2zxgx6DpE130_assertion evidence source_evidence_literature NP541605.RAjRTB3qC1IUYgpf5av0lWG-gdlqSeC5ekLx2zxgx6DpE130_provenance.
- NP541605.RAjRTB3qC1IUYgpf5av0lWG-gdlqSeC5ekLx2zxgx6DpE130_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." NP541605.RAjRTB3qC1IUYgpf5av0lWG-gdlqSeC5ekLx2zxgx6DpE130_provenance.