Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP966547.RAmNTfc9seCoa2IOrOCXyzNEsuC_nYOgrSrtZ2LWtLWDw130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP966547.RAmNTfc9seCoa2IOrOCXyzNEsuC_nYOgrSrtZ2LWtLWDw130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP966547.RAmNTfc9seCoa2IOrOCXyzNEsuC_nYOgrSrtZ2LWtLWDw130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP966547.RAmNTfc9seCoa2IOrOCXyzNEsuC_nYOgrSrtZ2LWtLWDw130_provenance.
- NP966547.RAmNTfc9seCoa2IOrOCXyzNEsuC_nYOgrSrtZ2LWtLWDw130_assertion description "[Twenty-five ADA*1/*2 heterozygotes (12.5%) and 2 ADA*2/*2 homozygotes (1%) were found in the control group, while only 10 *1/*2 heterozygotes (5.9%) and no *2/*2 homozygotes were found in the CAD group.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP966547.RAmNTfc9seCoa2IOrOCXyzNEsuC_nYOgrSrtZ2LWtLWDw130_provenance.
- NP966547.RAmNTfc9seCoa2IOrOCXyzNEsuC_nYOgrSrtZ2LWtLWDw130_assertion evidence source_evidence_literature NP966547.RAmNTfc9seCoa2IOrOCXyzNEsuC_nYOgrSrtZ2LWtLWDw130_provenance.
- NP966547.RAmNTfc9seCoa2IOrOCXyzNEsuC_nYOgrSrtZ2LWtLWDw130_assertion SIO_000772 17287605 NP966547.RAmNTfc9seCoa2IOrOCXyzNEsuC_nYOgrSrtZ2LWtLWDw130_provenance.
- NP966547.RAmNTfc9seCoa2IOrOCXyzNEsuC_nYOgrSrtZ2LWtLWDw130_assertion wasDerivedFrom befree-20150227 NP966547.RAmNTfc9seCoa2IOrOCXyzNEsuC_nYOgrSrtZ2LWtLWDw130_provenance.
- NP966547.RAmNTfc9seCoa2IOrOCXyzNEsuC_nYOgrSrtZ2LWtLWDw130_assertion wasGeneratedBy ECO_0000203 NP966547.RAmNTfc9seCoa2IOrOCXyzNEsuC_nYOgrSrtZ2LWtLWDw130_provenance.
- befree-20150227 importedOn "2015-02-27" NP966547.RAmNTfc9seCoa2IOrOCXyzNEsuC_nYOgrSrtZ2LWtLWDw130_provenance.