Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP800973.RALy0hp49STymyENr3el8bWixT3PJBtJCYjb8w_KrwIJM130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP800973.RALy0hp49STymyENr3el8bWixT3PJBtJCYjb8w_KrwIJM130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP800973.RALy0hp49STymyENr3el8bWixT3PJBtJCYjb8w_KrwIJM130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP800973.RALy0hp49STymyENr3el8bWixT3PJBtJCYjb8w_KrwIJM130_provenance.
- NP800973.RALy0hp49STymyENr3el8bWixT3PJBtJCYjb8w_KrwIJM130_assertion description "[We previously reported that the G/G genotype of single nucleotide polymorphism (SNP) at -420 (rs1862513) in the human resistin gene (RETN) increased susceptibility to type 2 diabetes by enhancing its promoter activity.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP800973.RALy0hp49STymyENr3el8bWixT3PJBtJCYjb8w_KrwIJM130_provenance.
- NP800973.RALy0hp49STymyENr3el8bWixT3PJBtJCYjb8w_KrwIJM130_assertion evidence source_evidence_literature NP800973.RALy0hp49STymyENr3el8bWixT3PJBtJCYjb8w_KrwIJM130_provenance.
- NP800973.RALy0hp49STymyENr3el8bWixT3PJBtJCYjb8w_KrwIJM130_assertion SIO_000772 20300528 NP800973.RALy0hp49STymyENr3el8bWixT3PJBtJCYjb8w_KrwIJM130_provenance.
- NP800973.RALy0hp49STymyENr3el8bWixT3PJBtJCYjb8w_KrwIJM130_assertion wasDerivedFrom befree-2016 NP800973.RALy0hp49STymyENr3el8bWixT3PJBtJCYjb8w_KrwIJM130_provenance.
- NP800973.RALy0hp49STymyENr3el8bWixT3PJBtJCYjb8w_KrwIJM130_assertion wasGeneratedBy ECO_0000203 NP800973.RALy0hp49STymyENr3el8bWixT3PJBtJCYjb8w_KrwIJM130_provenance.
- befree-2016 importedOn "2016-02-19" NP800973.RALy0hp49STymyENr3el8bWixT3PJBtJCYjb8w_KrwIJM130_provenance.