Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP477613.RAEtWkVdHxGNtBT3jwOLKUwcdpYgs58DS5OLCJ4zpa50o130_assertion> ?p ?o ?g. }
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- NP477613.RAEtWkVdHxGNtBT3jwOLKUwcdpYgs58DS5OLCJ4zpa50o130_assertion type Assertion NP477613.RAEtWkVdHxGNtBT3jwOLKUwcdpYgs58DS5OLCJ4zpa50o130_head.
- NP477613.RAEtWkVdHxGNtBT3jwOLKUwcdpYgs58DS5OLCJ4zpa50o130_assertion description "[Hereditary spastic paraplegia with cerebellar ataxia: a complex phenotype associated with a new SPG4 gene mutation.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP477613.RAEtWkVdHxGNtBT3jwOLKUwcdpYgs58DS5OLCJ4zpa50o130_provenance.
- NP477613.RAEtWkVdHxGNtBT3jwOLKUwcdpYgs58DS5OLCJ4zpa50o130_assertion evidence source_evidence_literature NP477613.RAEtWkVdHxGNtBT3jwOLKUwcdpYgs58DS5OLCJ4zpa50o130_provenance.
- NP477613.RAEtWkVdHxGNtBT3jwOLKUwcdpYgs58DS5OLCJ4zpa50o130_assertion SIO_000772 15667412 NP477613.RAEtWkVdHxGNtBT3jwOLKUwcdpYgs58DS5OLCJ4zpa50o130_provenance.
- NP477613.RAEtWkVdHxGNtBT3jwOLKUwcdpYgs58DS5OLCJ4zpa50o130_assertion wasDerivedFrom befree-2016 NP477613.RAEtWkVdHxGNtBT3jwOLKUwcdpYgs58DS5OLCJ4zpa50o130_provenance.
- NP477613.RAEtWkVdHxGNtBT3jwOLKUwcdpYgs58DS5OLCJ4zpa50o130_assertion wasGeneratedBy ECO_0000203 NP477613.RAEtWkVdHxGNtBT3jwOLKUwcdpYgs58DS5OLCJ4zpa50o130_provenance.