Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP333855.RA4W_Hl1qaOxQVaoCT0g_jm5F6bjAtpwrfNdRSRTClefs130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP333855.RA4W_Hl1qaOxQVaoCT0g_jm5F6bjAtpwrfNdRSRTClefs130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP333855.RA4W_Hl1qaOxQVaoCT0g_jm5F6bjAtpwrfNdRSRTClefs130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP333855.RA4W_Hl1qaOxQVaoCT0g_jm5F6bjAtpwrfNdRSRTClefs130_provenance.
- NP333855.RA4W_Hl1qaOxQVaoCT0g_jm5F6bjAtpwrfNdRSRTClefs130_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." NP333855.RA4W_Hl1qaOxQVaoCT0g_jm5F6bjAtpwrfNdRSRTClefs130_provenance.
- NP333855.RA4W_Hl1qaOxQVaoCT0g_jm5F6bjAtpwrfNdRSRTClefs130_assertion evidence source_evidence_literature NP333855.RA4W_Hl1qaOxQVaoCT0g_jm5F6bjAtpwrfNdRSRTClefs130_provenance.
- NP333855.RA4W_Hl1qaOxQVaoCT0g_jm5F6bjAtpwrfNdRSRTClefs130_assertion SIO_000772 12853462 NP333855.RA4W_Hl1qaOxQVaoCT0g_jm5F6bjAtpwrfNdRSRTClefs130_provenance.
- NP333855.RA4W_Hl1qaOxQVaoCT0g_jm5F6bjAtpwrfNdRSRTClefs130_assertion wasDerivedFrom befree-20150227 NP333855.RA4W_Hl1qaOxQVaoCT0g_jm5F6bjAtpwrfNdRSRTClefs130_provenance.
- NP333855.RA4W_Hl1qaOxQVaoCT0g_jm5F6bjAtpwrfNdRSRTClefs130_assertion wasGeneratedBy ECO_0000203 NP333855.RA4W_Hl1qaOxQVaoCT0g_jm5F6bjAtpwrfNdRSRTClefs130_provenance.
- befree-20150227 importedOn "2015-02-27" NP333855.RA4W_Hl1qaOxQVaoCT0g_jm5F6bjAtpwrfNdRSRTClefs130_provenance.