Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP337246.RAp-1dHZej5gzV4gBilvPER2zcr4DgYCIlv8YFcdGSe2s130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP337246.RAp-1dHZej5gzV4gBilvPER2zcr4DgYCIlv8YFcdGSe2s130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP337246.RAp-1dHZej5gzV4gBilvPER2zcr4DgYCIlv8YFcdGSe2s130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP337246.RAp-1dHZej5gzV4gBilvPER2zcr4DgYCIlv8YFcdGSe2s130_provenance.
- NP337246.RAp-1dHZej5gzV4gBilvPER2zcr4DgYCIlv8YFcdGSe2s130_assertion description "[Mutations in the gene encoding cystatin B (CSTB), a cysteine protease inhibitor, are responsible for the primary defect in Unverricht-Lundborg disease.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP337246.RAp-1dHZej5gzV4gBilvPER2zcr4DgYCIlv8YFcdGSe2s130_provenance.
- NP337246.RAp-1dHZej5gzV4gBilvPER2zcr4DgYCIlv8YFcdGSe2s130_assertion evidence source_evidence_literature NP337246.RAp-1dHZej5gzV4gBilvPER2zcr4DgYCIlv8YFcdGSe2s130_provenance.
- NP337246.RAp-1dHZej5gzV4gBilvPER2zcr4DgYCIlv8YFcdGSe2s130_assertion SIO_000772 12853462 NP337246.RAp-1dHZej5gzV4gBilvPER2zcr4DgYCIlv8YFcdGSe2s130_provenance.
- NP337246.RAp-1dHZej5gzV4gBilvPER2zcr4DgYCIlv8YFcdGSe2s130_assertion wasDerivedFrom befree-20150227 NP337246.RAp-1dHZej5gzV4gBilvPER2zcr4DgYCIlv8YFcdGSe2s130_provenance.
- NP337246.RAp-1dHZej5gzV4gBilvPER2zcr4DgYCIlv8YFcdGSe2s130_assertion wasGeneratedBy ECO_0000203 NP337246.RAp-1dHZej5gzV4gBilvPER2zcr4DgYCIlv8YFcdGSe2s130_provenance.
- befree-20150227 importedOn "2015-02-27" NP337246.RAp-1dHZej5gzV4gBilvPER2zcr4DgYCIlv8YFcdGSe2s130_provenance.