Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP636940.RAxMTyD2fTg1jaqVSTFO5CWXHY2Mk7x5WmzgOz-3omohc130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP636940.RAxMTyD2fTg1jaqVSTFO5CWXHY2Mk7x5WmzgOz-3omohc130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP636940.RAxMTyD2fTg1jaqVSTFO5CWXHY2Mk7x5WmzgOz-3omohc130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP636940.RAxMTyD2fTg1jaqVSTFO5CWXHY2Mk7x5WmzgOz-3omohc130_provenance.
- NP636940.RAxMTyD2fTg1jaqVSTFO5CWXHY2Mk7x5WmzgOz-3omohc130_assertion description "[Mutations and deletions in the SPG4 gene are responsible for up to 40% of autosomal dominant hereditary spastic paraplegia (HSP).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP636940.RAxMTyD2fTg1jaqVSTFO5CWXHY2Mk7x5WmzgOz-3omohc130_provenance.
- NP636940.RAxMTyD2fTg1jaqVSTFO5CWXHY2Mk7x5WmzgOz-3omohc130_assertion evidence source_evidence_literature NP636940.RAxMTyD2fTg1jaqVSTFO5CWXHY2Mk7x5WmzgOz-3omohc130_provenance.
- NP636940.RAxMTyD2fTg1jaqVSTFO5CWXHY2Mk7x5WmzgOz-3omohc130_assertion SIO_000772 17957230 NP636940.RAxMTyD2fTg1jaqVSTFO5CWXHY2Mk7x5WmzgOz-3omohc130_provenance.
- NP636940.RAxMTyD2fTg1jaqVSTFO5CWXHY2Mk7x5WmzgOz-3omohc130_assertion wasDerivedFrom befree-2016 NP636940.RAxMTyD2fTg1jaqVSTFO5CWXHY2Mk7x5WmzgOz-3omohc130_provenance.
- NP636940.RAxMTyD2fTg1jaqVSTFO5CWXHY2Mk7x5WmzgOz-3omohc130_assertion wasGeneratedBy ECO_0000203 NP636940.RAxMTyD2fTg1jaqVSTFO5CWXHY2Mk7x5WmzgOz-3omohc130_provenance.
- befree-2016 importedOn "2016-02-19" NP636940.RAxMTyD2fTg1jaqVSTFO5CWXHY2Mk7x5WmzgOz-3omohc130_provenance.