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- source_evidence_literature type ECO_0000212 NP631521.RA00YM5EaP68AOdEmMrh9ZecUlIoUY3MQl-OSslkg5WeM130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP631521.RA00YM5EaP68AOdEmMrh9ZecUlIoUY3MQl-OSslkg5WeM130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP631521.RA00YM5EaP68AOdEmMrh9ZecUlIoUY3MQl-OSslkg5WeM130_provenance.
- NP631521.RA00YM5EaP68AOdEmMrh9ZecUlIoUY3MQl-OSslkg5WeM130_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." NP631521.RA00YM5EaP68AOdEmMrh9ZecUlIoUY3MQl-OSslkg5WeM130_provenance.
- NP631521.RA00YM5EaP68AOdEmMrh9ZecUlIoUY3MQl-OSslkg5WeM130_assertion evidence source_evidence_literature NP631521.RA00YM5EaP68AOdEmMrh9ZecUlIoUY3MQl-OSslkg5WeM130_provenance.
- NP631521.RA00YM5EaP68AOdEmMrh9ZecUlIoUY3MQl-OSslkg5WeM130_assertion SIO_000772 23592921 NP631521.RA00YM5EaP68AOdEmMrh9ZecUlIoUY3MQl-OSslkg5WeM130_provenance.
- NP631521.RA00YM5EaP68AOdEmMrh9ZecUlIoUY3MQl-OSslkg5WeM130_assertion wasDerivedFrom befree-20140225 NP631521.RA00YM5EaP68AOdEmMrh9ZecUlIoUY3MQl-OSslkg5WeM130_provenance.
- NP631521.RA00YM5EaP68AOdEmMrh9ZecUlIoUY3MQl-OSslkg5WeM130_assertion wasGeneratedBy ECO_0000203 NP631521.RA00YM5EaP68AOdEmMrh9ZecUlIoUY3MQl-OSslkg5WeM130_provenance.
- befree-20140225 importedOn "2014-02-25" NP631521.RA00YM5EaP68AOdEmMrh9ZecUlIoUY3MQl-OSslkg5WeM130_provenance.