Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP333826.RAe2S_KwP0cyNOWFF7UrFcBH2SEre3ktklc0QJQHwaZI4130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP333826.RAe2S_KwP0cyNOWFF7UrFcBH2SEre3ktklc0QJQHwaZI4130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP333826.RAe2S_KwP0cyNOWFF7UrFcBH2SEre3ktklc0QJQHwaZI4130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP333826.RAe2S_KwP0cyNOWFF7UrFcBH2SEre3ktklc0QJQHwaZI4130_provenance.
- NP333826.RAe2S_KwP0cyNOWFF7UrFcBH2SEre3ktklc0QJQHwaZI4130_assertion description "[CSTB-deficient mice, produced by targeted disruption of the mouse Cstb gene, display a phenotype similar to the human disease, with progressive ataxia and myoclonic seizures.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP333826.RAe2S_KwP0cyNOWFF7UrFcBH2SEre3ktklc0QJQHwaZI4130_provenance.
- NP333826.RAe2S_KwP0cyNOWFF7UrFcBH2SEre3ktklc0QJQHwaZI4130_assertion evidence source_evidence_literature NP333826.RAe2S_KwP0cyNOWFF7UrFcBH2SEre3ktklc0QJQHwaZI4130_provenance.
- NP333826.RAe2S_KwP0cyNOWFF7UrFcBH2SEre3ktklc0QJQHwaZI4130_assertion SIO_000772 12853462 NP333826.RAe2S_KwP0cyNOWFF7UrFcBH2SEre3ktklc0QJQHwaZI4130_provenance.
- NP333826.RAe2S_KwP0cyNOWFF7UrFcBH2SEre3ktklc0QJQHwaZI4130_assertion wasDerivedFrom befree-20150227 NP333826.RAe2S_KwP0cyNOWFF7UrFcBH2SEre3ktklc0QJQHwaZI4130_provenance.
- NP333826.RAe2S_KwP0cyNOWFF7UrFcBH2SEre3ktklc0QJQHwaZI4130_assertion wasGeneratedBy ECO_0000203 NP333826.RAe2S_KwP0cyNOWFF7UrFcBH2SEre3ktklc0QJQHwaZI4130_provenance.
- befree-20150227 importedOn "2015-02-27" NP333826.RAe2S_KwP0cyNOWFF7UrFcBH2SEre3ktklc0QJQHwaZI4130_provenance.