Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP748316.RAQe-RMec2LVGD5TeZnRYHDutO1_f-59Lsi7PlAF1F_Bs130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP748316.RAQe-RMec2LVGD5TeZnRYHDutO1_f-59Lsi7PlAF1F_Bs130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP748316.RAQe-RMec2LVGD5TeZnRYHDutO1_f-59Lsi7PlAF1F_Bs130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP748316.RAQe-RMec2LVGD5TeZnRYHDutO1_f-59Lsi7PlAF1F_Bs130_provenance.
- NP748316.RAQe-RMec2LVGD5TeZnRYHDutO1_f-59Lsi7PlAF1F_Bs130_assertion description "[The genetic defect was related to leptin and TNFR-II levels in DM1 patients.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP748316.RAQe-RMec2LVGD5TeZnRYHDutO1_f-59Lsi7PlAF1F_Bs130_provenance.
- NP748316.RAQe-RMec2LVGD5TeZnRYHDutO1_f-59Lsi7PlAF1F_Bs130_assertion evidence source_evidence_literature NP748316.RAQe-RMec2LVGD5TeZnRYHDutO1_f-59Lsi7PlAF1F_Bs130_provenance.
- NP748316.RAQe-RMec2LVGD5TeZnRYHDutO1_f-59Lsi7PlAF1F_Bs130_assertion SIO_000772 12355336 NP748316.RAQe-RMec2LVGD5TeZnRYHDutO1_f-59Lsi7PlAF1F_Bs130_provenance.
- NP748316.RAQe-RMec2LVGD5TeZnRYHDutO1_f-59Lsi7PlAF1F_Bs130_assertion wasDerivedFrom befree-20150227 NP748316.RAQe-RMec2LVGD5TeZnRYHDutO1_f-59Lsi7PlAF1F_Bs130_provenance.
- NP748316.RAQe-RMec2LVGD5TeZnRYHDutO1_f-59Lsi7PlAF1F_Bs130_assertion wasGeneratedBy ECO_0000203 NP748316.RAQe-RMec2LVGD5TeZnRYHDutO1_f-59Lsi7PlAF1F_Bs130_provenance.
- befree-20150227 importedOn "2015-02-27" NP748316.RAQe-RMec2LVGD5TeZnRYHDutO1_f-59Lsi7PlAF1F_Bs130_provenance.