Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP401402.RAejvSN1czCxIdlm30hDbItp78cpr8aKSQvvpRo-ShBto130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP401402.RAejvSN1czCxIdlm30hDbItp78cpr8aKSQvvpRo-ShBto130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP401402.RAejvSN1czCxIdlm30hDbItp78cpr8aKSQvvpRo-ShBto130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP401402.RAejvSN1czCxIdlm30hDbItp78cpr8aKSQvvpRo-ShBto130_provenance.
- NP401402.RAejvSN1czCxIdlm30hDbItp78cpr8aKSQvvpRo-ShBto130_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." NP401402.RAejvSN1czCxIdlm30hDbItp78cpr8aKSQvvpRo-ShBto130_provenance.
- NP401402.RAejvSN1czCxIdlm30hDbItp78cpr8aKSQvvpRo-ShBto130_assertion evidence source_evidence_literature NP401402.RAejvSN1czCxIdlm30hDbItp78cpr8aKSQvvpRo-ShBto130_provenance.
- NP401402.RAejvSN1czCxIdlm30hDbItp78cpr8aKSQvvpRo-ShBto130_assertion SIO_000772 12853462 NP401402.RAejvSN1czCxIdlm30hDbItp78cpr8aKSQvvpRo-ShBto130_provenance.
- NP401402.RAejvSN1czCxIdlm30hDbItp78cpr8aKSQvvpRo-ShBto130_assertion wasDerivedFrom befree-2016 NP401402.RAejvSN1czCxIdlm30hDbItp78cpr8aKSQvvpRo-ShBto130_provenance.
- NP401402.RAejvSN1czCxIdlm30hDbItp78cpr8aKSQvvpRo-ShBto130_assertion wasGeneratedBy ECO_0000203 NP401402.RAejvSN1czCxIdlm30hDbItp78cpr8aKSQvvpRo-ShBto130_provenance.
- befree-2016 importedOn "2016-02-19" NP401402.RAejvSN1czCxIdlm30hDbItp78cpr8aKSQvvpRo-ShBto130_provenance.