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- NP767392.RAmDbXtUROsymPK08ETumCFRIVz-nnmLXeiJzqUKzDcEA130_assertion type Assertion NP767392.RAmDbXtUROsymPK08ETumCFRIVz-nnmLXeiJzqUKzDcEA130_head.
- NP767392.RAmDbXtUROsymPK08ETumCFRIVz-nnmLXeiJzqUKzDcEA130_assertion wasGeneratedBy ECO_0000203 NP767392.RAmDbXtUROsymPK08ETumCFRIVz-nnmLXeiJzqUKzDcEA130_provenance.
- NP767392.RAmDbXtUROsymPK08ETumCFRIVz-nnmLXeiJzqUKzDcEA130_assertion wasDerivedFrom befree-2016 NP767392.RAmDbXtUROsymPK08ETumCFRIVz-nnmLXeiJzqUKzDcEA130_provenance.
- NP767392.RAmDbXtUROsymPK08ETumCFRIVz-nnmLXeiJzqUKzDcEA130_assertion SIO_000772 19804849 NP767392.RAmDbXtUROsymPK08ETumCFRIVz-nnmLXeiJzqUKzDcEA130_provenance.
- NP767392.RAmDbXtUROsymPK08ETumCFRIVz-nnmLXeiJzqUKzDcEA130_assertion evidence source_evidence_literature NP767392.RAmDbXtUROsymPK08ETumCFRIVz-nnmLXeiJzqUKzDcEA130_provenance.
- NP767392.RAmDbXtUROsymPK08ETumCFRIVz-nnmLXeiJzqUKzDcEA130_assertion description "[Furthermore, the assay can detect excess FMR1 methylation in 82% of females with full mutations, although the methylation did not correlate with intellectual disability.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP767392.RAmDbXtUROsymPK08ETumCFRIVz-nnmLXeiJzqUKzDcEA130_provenance.