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- source_evidence_literature type ECO_0000212 NP435419.RAENNeB0GKADA0iqTKceL8AuFLCxnXtjUDYbdM_j8HRQo130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP435419.RAENNeB0GKADA0iqTKceL8AuFLCxnXtjUDYbdM_j8HRQo130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP435419.RAENNeB0GKADA0iqTKceL8AuFLCxnXtjUDYbdM_j8HRQo130_provenance.
- NP435419.RAENNeB0GKADA0iqTKceL8AuFLCxnXtjUDYbdM_j8HRQo130_assertion description "[Genetic variation in the ABCA4 (ABCR) gene has been associated with several distinct retinal phenotypes, including Stargardt disease/fundus flavimaculatus (STGD/FFM), cone-rod dystrophy (CRD), retinitis pigmentosa (RP) and age-related macular degeneration.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP435419.RAENNeB0GKADA0iqTKceL8AuFLCxnXtjUDYbdM_j8HRQo130_provenance.
- NP435419.RAENNeB0GKADA0iqTKceL8AuFLCxnXtjUDYbdM_j8HRQo130_assertion evidence source_evidence_literature NP435419.RAENNeB0GKADA0iqTKceL8AuFLCxnXtjUDYbdM_j8HRQo130_provenance.
- NP435419.RAENNeB0GKADA0iqTKceL8AuFLCxnXtjUDYbdM_j8HRQo130_assertion SIO_000772 15017103 NP435419.RAENNeB0GKADA0iqTKceL8AuFLCxnXtjUDYbdM_j8HRQo130_provenance.
- NP435419.RAENNeB0GKADA0iqTKceL8AuFLCxnXtjUDYbdM_j8HRQo130_assertion wasDerivedFrom befree-2016 NP435419.RAENNeB0GKADA0iqTKceL8AuFLCxnXtjUDYbdM_j8HRQo130_provenance.
- NP435419.RAENNeB0GKADA0iqTKceL8AuFLCxnXtjUDYbdM_j8HRQo130_assertion wasGeneratedBy ECO_0000203 NP435419.RAENNeB0GKADA0iqTKceL8AuFLCxnXtjUDYbdM_j8HRQo130_provenance.
- befree-2016 importedOn "2016-02-19" NP435419.RAENNeB0GKADA0iqTKceL8AuFLCxnXtjUDYbdM_j8HRQo130_provenance.