Matches in Nanopublications for { <http://rdf.disgenet.org/nanopublications.trig#NP657262.RACoXEiD9a84WCxQvX9IyW2-MKk3qtivLD9sNUywbWdO4130_assertion> ?p ?o ?g. }
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- NP657262.RACoXEiD9a84WCxQvX9IyW2-MKk3qtivLD9sNUywbWdO4130_assertion type Assertion NP657262.RACoXEiD9a84WCxQvX9IyW2-MKk3qtivLD9sNUywbWdO4130_head.
- NP657262.RACoXEiD9a84WCxQvX9IyW2-MKk3qtivLD9sNUywbWdO4130_assertion description "[The new SPG7 gene mutation leads to a novel complicated autosomal recessive hereditary spastic paraparesis phenotype that widens the spectrum of different brain systems that are optionally affected in hereditary spastic paraplegia (HSP).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP657262.RACoXEiD9a84WCxQvX9IyW2-MKk3qtivLD9sNUywbWdO4130_provenance.
- NP657262.RACoXEiD9a84WCxQvX9IyW2-MKk3qtivLD9sNUywbWdO4130_assertion evidence source_evidence_literature NP657262.RACoXEiD9a84WCxQvX9IyW2-MKk3qtivLD9sNUywbWdO4130_provenance.
- NP657262.RACoXEiD9a84WCxQvX9IyW2-MKk3qtivLD9sNUywbWdO4130_assertion SIO_000772 17646629 NP657262.RACoXEiD9a84WCxQvX9IyW2-MKk3qtivLD9sNUywbWdO4130_provenance.
- NP657262.RACoXEiD9a84WCxQvX9IyW2-MKk3qtivLD9sNUywbWdO4130_assertion wasDerivedFrom befree-20140225 NP657262.RACoXEiD9a84WCxQvX9IyW2-MKk3qtivLD9sNUywbWdO4130_provenance.
- NP657262.RACoXEiD9a84WCxQvX9IyW2-MKk3qtivLD9sNUywbWdO4130_assertion wasGeneratedBy ECO_0000203 NP657262.RACoXEiD9a84WCxQvX9IyW2-MKk3qtivLD9sNUywbWdO4130_provenance.