Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP204777.RAxRd5j2OC-8v7SZMdsEwMnJ6yFI2wmr52weTic5VqKgA130_assertion> ?p ?o ?g. }
Showing items 1 to 6 of
6
with 100 items per page.
- NP204777.RAxRd5j2OC-8v7SZMdsEwMnJ6yFI2wmr52weTic5VqKgA130_assertion type Assertion NP204777.RAxRd5j2OC-8v7SZMdsEwMnJ6yFI2wmr52weTic5VqKgA130_head.
- NP204777.RAxRd5j2OC-8v7SZMdsEwMnJ6yFI2wmr52weTic5VqKgA130_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.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP204777.RAxRd5j2OC-8v7SZMdsEwMnJ6yFI2wmr52weTic5VqKgA130_provenance.
- NP204777.RAxRd5j2OC-8v7SZMdsEwMnJ6yFI2wmr52weTic5VqKgA130_assertion evidence source_evidence_literature NP204777.RAxRd5j2OC-8v7SZMdsEwMnJ6yFI2wmr52weTic5VqKgA130_provenance.
- NP204777.RAxRd5j2OC-8v7SZMdsEwMnJ6yFI2wmr52weTic5VqKgA130_assertion SIO_000772 17646629 NP204777.RAxRd5j2OC-8v7SZMdsEwMnJ6yFI2wmr52weTic5VqKgA130_provenance.
- NP204777.RAxRd5j2OC-8v7SZMdsEwMnJ6yFI2wmr52weTic5VqKgA130_assertion wasDerivedFrom lhgdn-20090331 NP204777.RAxRd5j2OC-8v7SZMdsEwMnJ6yFI2wmr52weTic5VqKgA130_provenance.
- NP204777.RAxRd5j2OC-8v7SZMdsEwMnJ6yFI2wmr52weTic5VqKgA130_assertion wasGeneratedBy ECO_0000203 NP204777.RAxRd5j2OC-8v7SZMdsEwMnJ6yFI2wmr52weTic5VqKgA130_provenance.