Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP505001.RATcwBjlx28j-_3dGPWkvAdp1XBU6Db8Pk-DO4A-OsQos130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP505001.RATcwBjlx28j-_3dGPWkvAdp1XBU6Db8Pk-DO4A-OsQos130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP505001.RATcwBjlx28j-_3dGPWkvAdp1XBU6Db8Pk-DO4A-OsQos130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP505001.RATcwBjlx28j-_3dGPWkvAdp1XBU6Db8Pk-DO4A-OsQos130_provenance.
- NP505001.RATcwBjlx28j-_3dGPWkvAdp1XBU6Db8Pk-DO4A-OsQos130_assertion description "[We investigated the following SNPs: -1082, -819, -592 in the promoter region of IL10 in a normal (control) population and selected diseases: breast cancer (BrCa), systemic lupus erythematosus (SLE), and B-cell chronic lymphocytic leukemia (B-CLL) by denaturing high-performance liquid chromatography (DHPLC) and found distinct genotype and haplotype patterns.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP505001.RATcwBjlx28j-_3dGPWkvAdp1XBU6Db8Pk-DO4A-OsQos130_provenance.
- NP505001.RATcwBjlx28j-_3dGPWkvAdp1XBU6Db8Pk-DO4A-OsQos130_assertion evidence source_evidence_literature NP505001.RATcwBjlx28j-_3dGPWkvAdp1XBU6Db8Pk-DO4A-OsQos130_provenance.
- NP505001.RATcwBjlx28j-_3dGPWkvAdp1XBU6Db8Pk-DO4A-OsQos130_assertion SIO_000772 16030322 NP505001.RATcwBjlx28j-_3dGPWkvAdp1XBU6Db8Pk-DO4A-OsQos130_provenance.
- NP505001.RATcwBjlx28j-_3dGPWkvAdp1XBU6Db8Pk-DO4A-OsQos130_assertion wasDerivedFrom befree-2016 NP505001.RATcwBjlx28j-_3dGPWkvAdp1XBU6Db8Pk-DO4A-OsQos130_provenance.
- NP505001.RATcwBjlx28j-_3dGPWkvAdp1XBU6Db8Pk-DO4A-OsQos130_assertion wasGeneratedBy ECO_0000203 NP505001.RATcwBjlx28j-_3dGPWkvAdp1XBU6Db8Pk-DO4A-OsQos130_provenance.
- befree-2016 importedOn "2016-02-19" NP505001.RATcwBjlx28j-_3dGPWkvAdp1XBU6Db8Pk-DO4A-OsQos130_provenance.