Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP262535.RAxfvrqQKFlC6s1Y9B8LwgtUjBhbScIeZpH377U0bLfw0130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP262535.RAxfvrqQKFlC6s1Y9B8LwgtUjBhbScIeZpH377U0bLfw0130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP262535.RAxfvrqQKFlC6s1Y9B8LwgtUjBhbScIeZpH377U0bLfw0130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP262535.RAxfvrqQKFlC6s1Y9B8LwgtUjBhbScIeZpH377U0bLfw0130_provenance.
- NP262535.RAxfvrqQKFlC6s1Y9B8LwgtUjBhbScIeZpH377U0bLfw0130_assertion description "[SPG7 is a newly identified gene involved in an autosomal recessive form of hereditary spastic paraplegia (HSP), a genetically heterogeneous group of neurodegenerative disorders.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP262535.RAxfvrqQKFlC6s1Y9B8LwgtUjBhbScIeZpH377U0bLfw0130_provenance.
- NP262535.RAxfvrqQKFlC6s1Y9B8LwgtUjBhbScIeZpH377U0bLfw0130_assertion evidence source_evidence_literature NP262535.RAxfvrqQKFlC6s1Y9B8LwgtUjBhbScIeZpH377U0bLfw0130_provenance.
- NP262535.RAxfvrqQKFlC6s1Y9B8LwgtUjBhbScIeZpH377U0bLfw0130_assertion SIO_000772 10480368 NP262535.RAxfvrqQKFlC6s1Y9B8LwgtUjBhbScIeZpH377U0bLfw0130_provenance.
- NP262535.RAxfvrqQKFlC6s1Y9B8LwgtUjBhbScIeZpH377U0bLfw0130_assertion wasDerivedFrom befree-2016 NP262535.RAxfvrqQKFlC6s1Y9B8LwgtUjBhbScIeZpH377U0bLfw0130_provenance.
- NP262535.RAxfvrqQKFlC6s1Y9B8LwgtUjBhbScIeZpH377U0bLfw0130_assertion wasGeneratedBy ECO_0000203 NP262535.RAxfvrqQKFlC6s1Y9B8LwgtUjBhbScIeZpH377U0bLfw0130_provenance.
- befree-2016 importedOn "2016-02-19" NP262535.RAxfvrqQKFlC6s1Y9B8LwgtUjBhbScIeZpH377U0bLfw0130_provenance.