Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP413393.RAhx5YzPoRs_qEKWPejVKg8kWWrSgSXlHFBUVADhkf0j8130_assertion> ?p ?o ?g. }
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- NP413393.RAhx5YzPoRs_qEKWPejVKg8kWWrSgSXlHFBUVADhkf0j8130_assertion type Assertion NP413393.RAhx5YzPoRs_qEKWPejVKg8kWWrSgSXlHFBUVADhkf0j8130_head.
- NP413393.RAhx5YzPoRs_qEKWPejVKg8kWWrSgSXlHFBUVADhkf0j8130_assertion description "[The data are consistent with robust transcription of FTL in the lens, and suggest that whereas variations clustered in the IRE of the FTL gene are directly associated with hereditary hyperferritinemia-cataract syndrome, such IRE variations are unlikely to play a significant role in the genetic etiology of age-related cataract.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP413393.RAhx5YzPoRs_qEKWPejVKg8kWWrSgSXlHFBUVADhkf0j8130_provenance.
- NP413393.RAhx5YzPoRs_qEKWPejVKg8kWWrSgSXlHFBUVADhkf0j8130_assertion evidence source_evidence_literature NP413393.RAhx5YzPoRs_qEKWPejVKg8kWWrSgSXlHFBUVADhkf0j8130_provenance.
- NP413393.RAhx5YzPoRs_qEKWPejVKg8kWWrSgSXlHFBUVADhkf0j8130_assertion SIO_000772 23592921 NP413393.RAhx5YzPoRs_qEKWPejVKg8kWWrSgSXlHFBUVADhkf0j8130_provenance.
- NP413393.RAhx5YzPoRs_qEKWPejVKg8kWWrSgSXlHFBUVADhkf0j8130_assertion wasDerivedFrom befree-20150227 NP413393.RAhx5YzPoRs_qEKWPejVKg8kWWrSgSXlHFBUVADhkf0j8130_provenance.
- NP413393.RAhx5YzPoRs_qEKWPejVKg8kWWrSgSXlHFBUVADhkf0j8130_assertion wasGeneratedBy ECO_0000203 NP413393.RAhx5YzPoRs_qEKWPejVKg8kWWrSgSXlHFBUVADhkf0j8130_provenance.