Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP619732.RAIbYoKs0NF0qSgrDXxp5jubn2DlP5yw5avZv-MqLvIEs130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP619732.RAIbYoKs0NF0qSgrDXxp5jubn2DlP5yw5avZv-MqLvIEs130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP619732.RAIbYoKs0NF0qSgrDXxp5jubn2DlP5yw5avZv-MqLvIEs130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP619732.RAIbYoKs0NF0qSgrDXxp5jubn2DlP5yw5avZv-MqLvIEs130_provenance.
- NP619732.RAIbYoKs0NF0qSgrDXxp5jubn2DlP5yw5avZv-MqLvIEs130_assertion description "[In this study, in order to determine the role of CCR2, a receptor for MCP-1, in the development of CAD, we initially sequenced and identified the genetic variants of CCR2 using 24 unrelated Korean individuals' DNA samples.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP619732.RAIbYoKs0NF0qSgrDXxp5jubn2DlP5yw5avZv-MqLvIEs130_provenance.
- NP619732.RAIbYoKs0NF0qSgrDXxp5jubn2DlP5yw5avZv-MqLvIEs130_assertion evidence source_evidence_literature NP619732.RAIbYoKs0NF0qSgrDXxp5jubn2DlP5yw5avZv-MqLvIEs130_provenance.
- NP619732.RAIbYoKs0NF0qSgrDXxp5jubn2DlP5yw5avZv-MqLvIEs130_assertion SIO_000772 17482150 NP619732.RAIbYoKs0NF0qSgrDXxp5jubn2DlP5yw5avZv-MqLvIEs130_provenance.
- NP619732.RAIbYoKs0NF0qSgrDXxp5jubn2DlP5yw5avZv-MqLvIEs130_assertion wasDerivedFrom befree-20140225 NP619732.RAIbYoKs0NF0qSgrDXxp5jubn2DlP5yw5avZv-MqLvIEs130_provenance.
- NP619732.RAIbYoKs0NF0qSgrDXxp5jubn2DlP5yw5avZv-MqLvIEs130_assertion wasGeneratedBy ECO_0000203 NP619732.RAIbYoKs0NF0qSgrDXxp5jubn2DlP5yw5avZv-MqLvIEs130_provenance.
- befree-20140225 importedOn "2014-02-25" NP619732.RAIbYoKs0NF0qSgrDXxp5jubn2DlP5yw5avZv-MqLvIEs130_provenance.