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- source_evidence_literature type ECO_0000212 NP812645.RAo4eqV8NR4n7oW6IWYXrZmJj1x_tld6X7mM9qj-6-cFA130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP812645.RAo4eqV8NR4n7oW6IWYXrZmJj1x_tld6X7mM9qj-6-cFA130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP812645.RAo4eqV8NR4n7oW6IWYXrZmJj1x_tld6X7mM9qj-6-cFA130_provenance.
- NP812645.RAo4eqV8NR4n7oW6IWYXrZmJj1x_tld6X7mM9qj-6-cFA130_assertion description "[We propose that familial cortical myoclonus is a novel movement disorder that may be caused by mutation in NOL3.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP812645.RAo4eqV8NR4n7oW6IWYXrZmJj1x_tld6X7mM9qj-6-cFA130_provenance.
- NP812645.RAo4eqV8NR4n7oW6IWYXrZmJj1x_tld6X7mM9qj-6-cFA130_assertion evidence source_evidence_literature NP812645.RAo4eqV8NR4n7oW6IWYXrZmJj1x_tld6X7mM9qj-6-cFA130_provenance.
- NP812645.RAo4eqV8NR4n7oW6IWYXrZmJj1x_tld6X7mM9qj-6-cFA130_assertion SIO_000772 22926851 NP812645.RAo4eqV8NR4n7oW6IWYXrZmJj1x_tld6X7mM9qj-6-cFA130_provenance.
- NP812645.RAo4eqV8NR4n7oW6IWYXrZmJj1x_tld6X7mM9qj-6-cFA130_assertion wasDerivedFrom befree-20150227 NP812645.RAo4eqV8NR4n7oW6IWYXrZmJj1x_tld6X7mM9qj-6-cFA130_provenance.
- NP812645.RAo4eqV8NR4n7oW6IWYXrZmJj1x_tld6X7mM9qj-6-cFA130_assertion wasGeneratedBy ECO_0000203 NP812645.RAo4eqV8NR4n7oW6IWYXrZmJj1x_tld6X7mM9qj-6-cFA130_provenance.
- befree-20150227 importedOn "2015-02-27" NP812645.RAo4eqV8NR4n7oW6IWYXrZmJj1x_tld6X7mM9qj-6-cFA130_provenance.