Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP52881.RAgCoKBOX4IvCfJwNlWbq0wVfJGYvhEAVzir4tAzJl6pE130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP52881.RAgCoKBOX4IvCfJwNlWbq0wVfJGYvhEAVzir4tAzJl6pE130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP52881.RAgCoKBOX4IvCfJwNlWbq0wVfJGYvhEAVzir4tAzJl6pE130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP52881.RAgCoKBOX4IvCfJwNlWbq0wVfJGYvhEAVzir4tAzJl6pE130_provenance.
- NP52881.RAgCoKBOX4IvCfJwNlWbq0wVfJGYvhEAVzir4tAzJl6pE130_assertion description "[Addition of common genetic variants to traditional risk factors may be an effective method for discriminating young stroke patients at different risk of future ischemic events.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP52881.RAgCoKBOX4IvCfJwNlWbq0wVfJGYvhEAVzir4tAzJl6pE130_provenance.
- NP52881.RAgCoKBOX4IvCfJwNlWbq0wVfJGYvhEAVzir4tAzJl6pE130_assertion evidence source_evidence_literature NP52881.RAgCoKBOX4IvCfJwNlWbq0wVfJGYvhEAVzir4tAzJl6pE130_provenance.
- NP52881.RAgCoKBOX4IvCfJwNlWbq0wVfJGYvhEAVzir4tAzJl6pE130_assertion SIO_000772 19720979 NP52881.RAgCoKBOX4IvCfJwNlWbq0wVfJGYvhEAVzir4tAzJl6pE130_provenance.
- NP52881.RAgCoKBOX4IvCfJwNlWbq0wVfJGYvhEAVzir4tAzJl6pE130_assertion wasDerivedFrom gad-20150221 NP52881.RAgCoKBOX4IvCfJwNlWbq0wVfJGYvhEAVzir4tAzJl6pE130_provenance.
- NP52881.RAgCoKBOX4IvCfJwNlWbq0wVfJGYvhEAVzir4tAzJl6pE130_assertion wasGeneratedBy ECO_0000203 NP52881.RAgCoKBOX4IvCfJwNlWbq0wVfJGYvhEAVzir4tAzJl6pE130_provenance.
- gad-20150221 importedOn "2015-02-21" NP52881.RAgCoKBOX4IvCfJwNlWbq0wVfJGYvhEAVzir4tAzJl6pE130_provenance.