Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP709978.RAM5JnRnbODv8kDhWS7VNjmh-bsocG_qfaW73sCrgmKXg130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP709978.RAM5JnRnbODv8kDhWS7VNjmh-bsocG_qfaW73sCrgmKXg130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP709978.RAM5JnRnbODv8kDhWS7VNjmh-bsocG_qfaW73sCrgmKXg130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP709978.RAM5JnRnbODv8kDhWS7VNjmh-bsocG_qfaW73sCrgmKXg130_provenance.
- NP709978.RAM5JnRnbODv8kDhWS7VNjmh-bsocG_qfaW73sCrgmKXg130_assertion description "[Peripheral neuropathy in hereditary spastic paraplegia due to spastin (SPG4) mutation--a neurophysiological study using excitability techniques.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP709978.RAM5JnRnbODv8kDhWS7VNjmh-bsocG_qfaW73sCrgmKXg130_provenance.
- NP709978.RAM5JnRnbODv8kDhWS7VNjmh-bsocG_qfaW73sCrgmKXg130_assertion evidence source_evidence_literature NP709978.RAM5JnRnbODv8kDhWS7VNjmh-bsocG_qfaW73sCrgmKXg130_provenance.
- NP709978.RAM5JnRnbODv8kDhWS7VNjmh-bsocG_qfaW73sCrgmKXg130_assertion SIO_000772 22192498 NP709978.RAM5JnRnbODv8kDhWS7VNjmh-bsocG_qfaW73sCrgmKXg130_provenance.
- NP709978.RAM5JnRnbODv8kDhWS7VNjmh-bsocG_qfaW73sCrgmKXg130_assertion wasDerivedFrom befree-20150227 NP709978.RAM5JnRnbODv8kDhWS7VNjmh-bsocG_qfaW73sCrgmKXg130_provenance.
- NP709978.RAM5JnRnbODv8kDhWS7VNjmh-bsocG_qfaW73sCrgmKXg130_assertion wasGeneratedBy ECO_0000203 NP709978.RAM5JnRnbODv8kDhWS7VNjmh-bsocG_qfaW73sCrgmKXg130_provenance.
- befree-20150227 importedOn "2015-02-27" NP709978.RAM5JnRnbODv8kDhWS7VNjmh-bsocG_qfaW73sCrgmKXg130_provenance.