Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP77226.RAbGbSvhYQKHtrq1YFXmxknO1DYGb509vi1Dr1k3z_ikM130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP77226.RAbGbSvhYQKHtrq1YFXmxknO1DYGb509vi1Dr1k3z_ikM130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP77226.RAbGbSvhYQKHtrq1YFXmxknO1DYGb509vi1Dr1k3z_ikM130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP77226.RAbGbSvhYQKHtrq1YFXmxknO1DYGb509vi1Dr1k3z_ikM130_provenance.
- gad-20150221 importedOn "2015-02-21" NP77226.RAbGbSvhYQKHtrq1YFXmxknO1DYGb509vi1Dr1k3z_ikM130_provenance.
- NP77226.RAbGbSvhYQKHtrq1YFXmxknO1DYGb509vi1Dr1k3z_ikM130_assertion wasGeneratedBy ECO_0000203 NP77226.RAbGbSvhYQKHtrq1YFXmxknO1DYGb509vi1Dr1k3z_ikM130_provenance.
- NP77226.RAbGbSvhYQKHtrq1YFXmxknO1DYGb509vi1Dr1k3z_ikM130_assertion wasDerivedFrom gad-20150221 NP77226.RAbGbSvhYQKHtrq1YFXmxknO1DYGb509vi1Dr1k3z_ikM130_provenance.
- NP77226.RAbGbSvhYQKHtrq1YFXmxknO1DYGb509vi1Dr1k3z_ikM130_assertion SIO_000772 12446192 NP77226.RAbGbSvhYQKHtrq1YFXmxknO1DYGb509vi1Dr1k3z_ikM130_provenance.
- NP77226.RAbGbSvhYQKHtrq1YFXmxknO1DYGb509vi1Dr1k3z_ikM130_assertion evidence source_evidence_literature NP77226.RAbGbSvhYQKHtrq1YFXmxknO1DYGb509vi1Dr1k3z_ikM130_provenance.
- NP77226.RAbGbSvhYQKHtrq1YFXmxknO1DYGb509vi1Dr1k3z_ikM130_assertion description "[ An increasing number of risk alleles are associated with an elevated risk for CAD. An analysis of multiple polymorphisms, some several hundred, each with a small impact, may allow improved assessment of the individual genetic burden for CAD. Larger studi]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP77226.RAbGbSvhYQKHtrq1YFXmxknO1DYGb509vi1Dr1k3z_ikM130_provenance.