Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP235062.RADgXXeCtM9DoopszDYaatXmNc85w2_cf20a2uW6vC8VE130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP235062.RADgXXeCtM9DoopszDYaatXmNc85w2_cf20a2uW6vC8VE130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP235062.RADgXXeCtM9DoopszDYaatXmNc85w2_cf20a2uW6vC8VE130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP235062.RADgXXeCtM9DoopszDYaatXmNc85w2_cf20a2uW6vC8VE130_provenance.
- NP235062.RADgXXeCtM9DoopszDYaatXmNc85w2_cf20a2uW6vC8VE130_assertion description "[The C-106T polymorphism was genotyped in 228 cases (microalbuminuria or overt proteinuria) and 220 controls (normoalbuminuria with diabetes duration > or =10 years) for a case-control comparison, and the association with erythrocyte AR content was investigated.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP235062.RADgXXeCtM9DoopszDYaatXmNc85w2_cf20a2uW6vC8VE130_provenance.
- NP235062.RADgXXeCtM9DoopszDYaatXmNc85w2_cf20a2uW6vC8VE130_assertion evidence source_evidence_literature NP235062.RADgXXeCtM9DoopszDYaatXmNc85w2_cf20a2uW6vC8VE130_provenance.
- NP235062.RADgXXeCtM9DoopszDYaatXmNc85w2_cf20a2uW6vC8VE130_assertion SIO_000772 14582038 NP235062.RADgXXeCtM9DoopszDYaatXmNc85w2_cf20a2uW6vC8VE130_provenance.
- NP235062.RADgXXeCtM9DoopszDYaatXmNc85w2_cf20a2uW6vC8VE130_assertion wasDerivedFrom befree-20150227 NP235062.RADgXXeCtM9DoopszDYaatXmNc85w2_cf20a2uW6vC8VE130_provenance.
- NP235062.RADgXXeCtM9DoopszDYaatXmNc85w2_cf20a2uW6vC8VE130_assertion wasGeneratedBy ECO_0000203 NP235062.RADgXXeCtM9DoopszDYaatXmNc85w2_cf20a2uW6vC8VE130_provenance.
- befree-20150227 importedOn "2015-02-27" NP235062.RADgXXeCtM9DoopszDYaatXmNc85w2_cf20a2uW6vC8VE130_provenance.