Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP262537.RAlrXptRtMniKonvzigC-rCmPhdmwnbG5kTGqKJWtu3lI130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP262537.RAlrXptRtMniKonvzigC-rCmPhdmwnbG5kTGqKJWtu3lI130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP262537.RAlrXptRtMniKonvzigC-rCmPhdmwnbG5kTGqKJWtu3lI130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP262537.RAlrXptRtMniKonvzigC-rCmPhdmwnbG5kTGqKJWtu3lI130_provenance.
- NP262537.RAlrXptRtMniKonvzigC-rCmPhdmwnbG5kTGqKJWtu3lI130_assertion description "[The provided genomic structure of SPG7 should facilitate the screening for mutations in this gene in patients with HSP and other related mitochondrial disease syndromes.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP262537.RAlrXptRtMniKonvzigC-rCmPhdmwnbG5kTGqKJWtu3lI130_provenance.
- NP262537.RAlrXptRtMniKonvzigC-rCmPhdmwnbG5kTGqKJWtu3lI130_assertion evidence source_evidence_literature NP262537.RAlrXptRtMniKonvzigC-rCmPhdmwnbG5kTGqKJWtu3lI130_provenance.
- NP262537.RAlrXptRtMniKonvzigC-rCmPhdmwnbG5kTGqKJWtu3lI130_assertion SIO_000772 10480368 NP262537.RAlrXptRtMniKonvzigC-rCmPhdmwnbG5kTGqKJWtu3lI130_provenance.
- NP262537.RAlrXptRtMniKonvzigC-rCmPhdmwnbG5kTGqKJWtu3lI130_assertion wasDerivedFrom befree-2016 NP262537.RAlrXptRtMniKonvzigC-rCmPhdmwnbG5kTGqKJWtu3lI130_provenance.
- NP262537.RAlrXptRtMniKonvzigC-rCmPhdmwnbG5kTGqKJWtu3lI130_assertion wasGeneratedBy ECO_0000203 NP262537.RAlrXptRtMniKonvzigC-rCmPhdmwnbG5kTGqKJWtu3lI130_provenance.
- befree-2016 importedOn "2016-02-19" NP262537.RAlrXptRtMniKonvzigC-rCmPhdmwnbG5kTGqKJWtu3lI130_provenance.