Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP418019.RA9_3MC4sqPkWENm5kW4rH--1q8AtfDWkTKYBGWXNloXI130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP418019.RA9_3MC4sqPkWENm5kW4rH--1q8AtfDWkTKYBGWXNloXI130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP418019.RA9_3MC4sqPkWENm5kW4rH--1q8AtfDWkTKYBGWXNloXI130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP418019.RA9_3MC4sqPkWENm5kW4rH--1q8AtfDWkTKYBGWXNloXI130_provenance.
- NP418019.RA9_3MC4sqPkWENm5kW4rH--1q8AtfDWkTKYBGWXNloXI130_assertion description "[GAP-43 levels were low in all disorders analysed (in particular motor neuron disease; p=0.001, and movement disorders and multiple sclerosis; p<0.0001) compared to controls, aside from CNS infections.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP418019.RA9_3MC4sqPkWENm5kW4rH--1q8AtfDWkTKYBGWXNloXI130_provenance.
- NP418019.RA9_3MC4sqPkWENm5kW4rH--1q8AtfDWkTKYBGWXNloXI130_assertion evidence source_evidence_literature NP418019.RA9_3MC4sqPkWENm5kW4rH--1q8AtfDWkTKYBGWXNloXI130_provenance.
- NP418019.RA9_3MC4sqPkWENm5kW4rH--1q8AtfDWkTKYBGWXNloXI130_assertion SIO_000772 25175067 NP418019.RA9_3MC4sqPkWENm5kW4rH--1q8AtfDWkTKYBGWXNloXI130_provenance.
- NP418019.RA9_3MC4sqPkWENm5kW4rH--1q8AtfDWkTKYBGWXNloXI130_assertion wasDerivedFrom befree-20150227 NP418019.RA9_3MC4sqPkWENm5kW4rH--1q8AtfDWkTKYBGWXNloXI130_provenance.
- NP418019.RA9_3MC4sqPkWENm5kW4rH--1q8AtfDWkTKYBGWXNloXI130_assertion wasGeneratedBy ECO_0000203 NP418019.RA9_3MC4sqPkWENm5kW4rH--1q8AtfDWkTKYBGWXNloXI130_provenance.
- befree-20150227 importedOn "2015-02-27" NP418019.RA9_3MC4sqPkWENm5kW4rH--1q8AtfDWkTKYBGWXNloXI130_provenance.