Matches in Nanopublications for { <http://rdf.disgenet.org/nanopublications.trig#NP527774.RADccuyaPgyNz4WMiPa4OGihOuFe6AcIhAKgdSfriydz4130_assertion> ?p ?o ?g. }
Showing items 1 to 6 of
6
with 100 items per page.
- NP527774.RADccuyaPgyNz4WMiPa4OGihOuFe6AcIhAKgdSfriydz4130_assertion type Assertion NP527774.RADccuyaPgyNz4WMiPa4OGihOuFe6AcIhAKgdSfriydz4130_head.
- NP527774.RADccuyaPgyNz4WMiPa4OGihOuFe6AcIhAKgdSfriydz4130_assertion description "[Mmutations in paraplegin, a putative mitochondrial metallopeptidase of the AAA family, cause an autosomal recessive form of hereditary spastic paraplegia (HSP).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP527774.RADccuyaPgyNz4WMiPa4OGihOuFe6AcIhAKgdSfriydz4130_provenance.
- NP527774.RADccuyaPgyNz4WMiPa4OGihOuFe6AcIhAKgdSfriydz4130_assertion evidence source_evidence_literature NP527774.RADccuyaPgyNz4WMiPa4OGihOuFe6AcIhAKgdSfriydz4130_provenance.
- NP527774.RADccuyaPgyNz4WMiPa4OGihOuFe6AcIhAKgdSfriydz4130_assertion SIO_000772 14623864 NP527774.RADccuyaPgyNz4WMiPa4OGihOuFe6AcIhAKgdSfriydz4130_provenance.
- NP527774.RADccuyaPgyNz4WMiPa4OGihOuFe6AcIhAKgdSfriydz4130_assertion wasDerivedFrom befree-20140225 NP527774.RADccuyaPgyNz4WMiPa4OGihOuFe6AcIhAKgdSfriydz4130_provenance.
- NP527774.RADccuyaPgyNz4WMiPa4OGihOuFe6AcIhAKgdSfriydz4130_assertion wasGeneratedBy ECO_0000203 NP527774.RADccuyaPgyNz4WMiPa4OGihOuFe6AcIhAKgdSfriydz4130_provenance.