Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP615644.RAHRYTqoe-3uhbWMp025XMI2YVo7puVUOBZRZTsl7EE3A130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP615644.RAHRYTqoe-3uhbWMp025XMI2YVo7puVUOBZRZTsl7EE3A130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP615644.RAHRYTqoe-3uhbWMp025XMI2YVo7puVUOBZRZTsl7EE3A130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP615644.RAHRYTqoe-3uhbWMp025XMI2YVo7puVUOBZRZTsl7EE3A130_provenance.
- NP615644.RAHRYTqoe-3uhbWMp025XMI2YVo7puVUOBZRZTsl7EE3A130_assertion description "[Three known vWF gene polymorphisms were genotyped in a group of 493 type I diabetic subjects, all showing proliferative retinopathy, but with various stages of renal involvement, which ranged from no microalbuminuria, despite a mean duration of diabetes of 31 years, to advanced nephropathy (GENEDIAB Study): Thr789Ala (Rsa I), M-/M+ (Msp I) (intron 19), and Ala1381Thr (Hph I).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP615644.RAHRYTqoe-3uhbWMp025XMI2YVo7puVUOBZRZTsl7EE3A130_provenance.
- NP615644.RAHRYTqoe-3uhbWMp025XMI2YVo7puVUOBZRZTsl7EE3A130_assertion evidence source_evidence_literature NP615644.RAHRYTqoe-3uhbWMp025XMI2YVo7puVUOBZRZTsl7EE3A130_provenance.
- NP615644.RAHRYTqoe-3uhbWMp025XMI2YVo7puVUOBZRZTsl7EE3A130_assertion SIO_000772 10760079 NP615644.RAHRYTqoe-3uhbWMp025XMI2YVo7puVUOBZRZTsl7EE3A130_provenance.
- NP615644.RAHRYTqoe-3uhbWMp025XMI2YVo7puVUOBZRZTsl7EE3A130_assertion wasDerivedFrom befree-20140225 NP615644.RAHRYTqoe-3uhbWMp025XMI2YVo7puVUOBZRZTsl7EE3A130_provenance.
- NP615644.RAHRYTqoe-3uhbWMp025XMI2YVo7puVUOBZRZTsl7EE3A130_assertion wasGeneratedBy ECO_0000203 NP615644.RAHRYTqoe-3uhbWMp025XMI2YVo7puVUOBZRZTsl7EE3A130_provenance.
- befree-20140225 importedOn "2014-02-25" NP615644.RAHRYTqoe-3uhbWMp025XMI2YVo7puVUOBZRZTsl7EE3A130_provenance.