Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP151082.RAsl9KPUeOy0aYFwQ0XVNUyhcIHjuWkP_eIOM9q7pwtBk130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP151082.RAsl9KPUeOy0aYFwQ0XVNUyhcIHjuWkP_eIOM9q7pwtBk130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP151082.RAsl9KPUeOy0aYFwQ0XVNUyhcIHjuWkP_eIOM9q7pwtBk130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP151082.RAsl9KPUeOy0aYFwQ0XVNUyhcIHjuWkP_eIOM9q7pwtBk130_provenance.
- NP151082.RAsl9KPUeOy0aYFwQ0XVNUyhcIHjuWkP_eIOM9q7pwtBk130_assertion description "[Sequence variation in the VEGFA gene is associated with risk of developing blinding DR in T1DM and T2DM.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP151082.RAsl9KPUeOy0aYFwQ0XVNUyhcIHjuWkP_eIOM9q7pwtBk130_provenance.
- NP151082.RAsl9KPUeOy0aYFwQ0XVNUyhcIHjuWkP_eIOM9q7pwtBk130_assertion evidence source_evidence_literature NP151082.RAsl9KPUeOy0aYFwQ0XVNUyhcIHjuWkP_eIOM9q7pwtBk130_provenance.
- NP151082.RAsl9KPUeOy0aYFwQ0XVNUyhcIHjuWkP_eIOM9q7pwtBk130_assertion SIO_000772 19553626 NP151082.RAsl9KPUeOy0aYFwQ0XVNUyhcIHjuWkP_eIOM9q7pwtBk130_provenance.
- NP151082.RAsl9KPUeOy0aYFwQ0XVNUyhcIHjuWkP_eIOM9q7pwtBk130_assertion wasDerivedFrom gad-20150221 NP151082.RAsl9KPUeOy0aYFwQ0XVNUyhcIHjuWkP_eIOM9q7pwtBk130_provenance.
- NP151082.RAsl9KPUeOy0aYFwQ0XVNUyhcIHjuWkP_eIOM9q7pwtBk130_assertion wasGeneratedBy ECO_0000203 NP151082.RAsl9KPUeOy0aYFwQ0XVNUyhcIHjuWkP_eIOM9q7pwtBk130_provenance.
- gad-20150221 importedOn "2015-02-21" NP151082.RAsl9KPUeOy0aYFwQ0XVNUyhcIHjuWkP_eIOM9q7pwtBk130_provenance.