Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP844537.RAUkhwexcVT7knHZ4G5t9rvRc8YwKDc3UXQQxPriGWWNQ130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP844537.RAUkhwexcVT7knHZ4G5t9rvRc8YwKDc3UXQQxPriGWWNQ130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP844537.RAUkhwexcVT7knHZ4G5t9rvRc8YwKDc3UXQQxPriGWWNQ130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP844537.RAUkhwexcVT7knHZ4G5t9rvRc8YwKDc3UXQQxPriGWWNQ130_provenance.
- NP844537.RAUkhwexcVT7knHZ4G5t9rvRc8YwKDc3UXQQxPriGWWNQ130_assertion description "[Mutational spectrum of the SPG4 (SPAST) and SPG3A (ATL1) genes in Spanish patients with hereditary spastic paraplegia.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP844537.RAUkhwexcVT7knHZ4G5t9rvRc8YwKDc3UXQQxPriGWWNQ130_provenance.
- NP844537.RAUkhwexcVT7knHZ4G5t9rvRc8YwKDc3UXQQxPriGWWNQ130_assertion evidence source_evidence_literature NP844537.RAUkhwexcVT7knHZ4G5t9rvRc8YwKDc3UXQQxPriGWWNQ130_provenance.
- NP844537.RAUkhwexcVT7knHZ4G5t9rvRc8YwKDc3UXQQxPriGWWNQ130_assertion SIO_000772 20932283 NP844537.RAUkhwexcVT7knHZ4G5t9rvRc8YwKDc3UXQQxPriGWWNQ130_provenance.
- NP844537.RAUkhwexcVT7knHZ4G5t9rvRc8YwKDc3UXQQxPriGWWNQ130_assertion wasDerivedFrom befree-2016 NP844537.RAUkhwexcVT7knHZ4G5t9rvRc8YwKDc3UXQQxPriGWWNQ130_provenance.
- NP844537.RAUkhwexcVT7knHZ4G5t9rvRc8YwKDc3UXQQxPriGWWNQ130_assertion wasGeneratedBy ECO_0000203 NP844537.RAUkhwexcVT7knHZ4G5t9rvRc8YwKDc3UXQQxPriGWWNQ130_provenance.
- befree-2016 importedOn "2016-02-19" NP844537.RAUkhwexcVT7knHZ4G5t9rvRc8YwKDc3UXQQxPriGWWNQ130_provenance.