Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP3210.RAsgD83L3rCqSXC-c9Id6_TeZ-rIgmHZrfi7rDkIRAsW8130_provenance>. }
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- source_evidence_curated type ECO_0000205 NP3210.RAsgD83L3rCqSXC-c9Id6_TeZ-rIgmHZrfi7rDkIRAsW8130_provenance.
- source_evidence_curated label "DisGeNET evidence - CURATED" NP3210.RAsgD83L3rCqSXC-c9Id6_TeZ-rIgmHZrfi7rDkIRAsW8130_provenance.
- source_evidence_curated comment "Gene-disease associations manually curated." NP3210.RAsgD83L3rCqSXC-c9Id6_TeZ-rIgmHZrfi7rDkIRAsW8130_provenance.
- 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.
- uniprot-2016 importedOn "2016-01-25" NP3210.RAsgD83L3rCqSXC-c9Id6_TeZ-rIgmHZrfi7rDkIRAsW8130_provenance.