Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP710063.RAOofpvzPzTh5WHlIl68hRnVyXojeP0BdGweBXEgZq6MM130_assertion> ?p ?o ?g. }
Showing items 1 to 6 of
6
with 100 items per page.
- NP710063.RAOofpvzPzTh5WHlIl68hRnVyXojeP0BdGweBXEgZq6MM130_assertion type Assertion NP710063.RAOofpvzPzTh5WHlIl68hRnVyXojeP0BdGweBXEgZq6MM130_head.
- NP710063.RAOofpvzPzTh5WHlIl68hRnVyXojeP0BdGweBXEgZq6MM130_assertion description "[We studied nine Italian families with a pure form of autosomal dominant spastic paraplegia (ADHSP) to assess the frequency of mutations in the SPG4 gene.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP710063.RAOofpvzPzTh5WHlIl68hRnVyXojeP0BdGweBXEgZq6MM130_provenance.
- NP710063.RAOofpvzPzTh5WHlIl68hRnVyXojeP0BdGweBXEgZq6MM130_assertion evidence source_evidence_literature NP710063.RAOofpvzPzTh5WHlIl68hRnVyXojeP0BdGweBXEgZq6MM130_provenance.
- NP710063.RAOofpvzPzTh5WHlIl68hRnVyXojeP0BdGweBXEgZq6MM130_assertion SIO_000772 11985387 NP710063.RAOofpvzPzTh5WHlIl68hRnVyXojeP0BdGweBXEgZq6MM130_provenance.
- NP710063.RAOofpvzPzTh5WHlIl68hRnVyXojeP0BdGweBXEgZq6MM130_assertion wasDerivedFrom befree-20150227 NP710063.RAOofpvzPzTh5WHlIl68hRnVyXojeP0BdGweBXEgZq6MM130_provenance.
- NP710063.RAOofpvzPzTh5WHlIl68hRnVyXojeP0BdGweBXEgZq6MM130_assertion wasGeneratedBy ECO_0000203 NP710063.RAOofpvzPzTh5WHlIl68hRnVyXojeP0BdGweBXEgZq6MM130_provenance.