Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP3210.RAsgD83L3rCqSXC-c9Id6_TeZ-rIgmHZrfi7rDkIRAsW8130_assertion> ?p ?o ?g. }
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- NP3210.RAsgD83L3rCqSXC-c9Id6_TeZ-rIgmHZrfi7rDkIRAsW8130_assertion type Assertion NP3210.RAsgD83L3rCqSXC-c9Id6_TeZ-rIgmHZrfi7rDkIRAsW8130_head.
- NP3210.RAsgD83L3rCqSXC-c9Id6_TeZ-rIgmHZrfi7rDkIRAsW8130_assertion description "[The most common form of hereditary spastic paraplegia is caused by mutations in the spastin gene (SPG4), which encodes spastin, an adenosine triphosphatase associated with various cellular activities protein.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP3210.RAsgD83L3rCqSXC-c9Id6_TeZ-rIgmHZrfi7rDkIRAsW8130_provenance.
- NP3210.RAsgD83L3rCqSXC-c9Id6_TeZ-rIgmHZrfi7rDkIRAsW8130_assertion evidence source_evidence_curated NP3210.RAsgD83L3rCqSXC-c9Id6_TeZ-rIgmHZrfi7rDkIRAsW8130_provenance.
- NP3210.RAsgD83L3rCqSXC-c9Id6_TeZ-rIgmHZrfi7rDkIRAsW8130_assertion SIO_000772 14732620 NP3210.RAsgD83L3rCqSXC-c9Id6_TeZ-rIgmHZrfi7rDkIRAsW8130_provenance.
- NP3210.RAsgD83L3rCqSXC-c9Id6_TeZ-rIgmHZrfi7rDkIRAsW8130_assertion wasDerivedFrom uniprot-2016 NP3210.RAsgD83L3rCqSXC-c9Id6_TeZ-rIgmHZrfi7rDkIRAsW8130_provenance.
- NP3210.RAsgD83L3rCqSXC-c9Id6_TeZ-rIgmHZrfi7rDkIRAsW8130_assertion wasGeneratedBy ECO_0000218 NP3210.RAsgD83L3rCqSXC-c9Id6_TeZ-rIgmHZrfi7rDkIRAsW8130_provenance.