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- NP1070060.RAvwpDOUbQ5Yc1UBMtjnKZdlRzI--WHoBiIZtfqn-sr1E130_assertion type Assertion NP1070060.RAvwpDOUbQ5Yc1UBMtjnKZdlRzI--WHoBiIZtfqn-sr1E130_head.
- NP1070060.RAvwpDOUbQ5Yc1UBMtjnKZdlRzI--WHoBiIZtfqn-sr1E130_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." NP1070060.RAvwpDOUbQ5Yc1UBMtjnKZdlRzI--WHoBiIZtfqn-sr1E130_provenance.
- NP1070060.RAvwpDOUbQ5Yc1UBMtjnKZdlRzI--WHoBiIZtfqn-sr1E130_assertion evidence source_evidence_literature NP1070060.RAvwpDOUbQ5Yc1UBMtjnKZdlRzI--WHoBiIZtfqn-sr1E130_provenance.
- NP1070060.RAvwpDOUbQ5Yc1UBMtjnKZdlRzI--WHoBiIZtfqn-sr1E130_assertion SIO_000772 23592921 NP1070060.RAvwpDOUbQ5Yc1UBMtjnKZdlRzI--WHoBiIZtfqn-sr1E130_provenance.
- NP1070060.RAvwpDOUbQ5Yc1UBMtjnKZdlRzI--WHoBiIZtfqn-sr1E130_assertion wasDerivedFrom befree-2016 NP1070060.RAvwpDOUbQ5Yc1UBMtjnKZdlRzI--WHoBiIZtfqn-sr1E130_provenance.
- NP1070060.RAvwpDOUbQ5Yc1UBMtjnKZdlRzI--WHoBiIZtfqn-sr1E130_assertion wasGeneratedBy ECO_0000203 NP1070060.RAvwpDOUbQ5Yc1UBMtjnKZdlRzI--WHoBiIZtfqn-sr1E130_provenance.