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- NP734361.RAWEqLppw0x6obrUv2XyqynTce_NkGcUo1WzQFGXBjJXo130_assertion type Assertion NP734361.RAWEqLppw0x6obrUv2XyqynTce_NkGcUo1WzQFGXBjJXo130_head.
- NP734361.RAWEqLppw0x6obrUv2XyqynTce_NkGcUo1WzQFGXBjJXo130_assertion description "[Because hypermagnesuria and hypocalciuria accompanied the hypomagnesemia, we analyzed genes associated with hypermagnesuria and detected highly conserved HNF1 recognition sites in FXYD2, a gene that can cause autosomal dominant hypomagnesemia and hypocalciuria when mutated.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP734361.RAWEqLppw0x6obrUv2XyqynTce_NkGcUo1WzQFGXBjJXo130_provenance.
- NP734361.RAWEqLppw0x6obrUv2XyqynTce_NkGcUo1WzQFGXBjJXo130_assertion evidence source_evidence_literature NP734361.RAWEqLppw0x6obrUv2XyqynTce_NkGcUo1WzQFGXBjJXo130_provenance.
- NP734361.RAWEqLppw0x6obrUv2XyqynTce_NkGcUo1WzQFGXBjJXo130_assertion SIO_000772 19389850 NP734361.RAWEqLppw0x6obrUv2XyqynTce_NkGcUo1WzQFGXBjJXo130_provenance.
- NP734361.RAWEqLppw0x6obrUv2XyqynTce_NkGcUo1WzQFGXBjJXo130_assertion wasDerivedFrom befree-2016 NP734361.RAWEqLppw0x6obrUv2XyqynTce_NkGcUo1WzQFGXBjJXo130_provenance.
- NP734361.RAWEqLppw0x6obrUv2XyqynTce_NkGcUo1WzQFGXBjJXo130_assertion wasGeneratedBy ECO_0000203 NP734361.RAWEqLppw0x6obrUv2XyqynTce_NkGcUo1WzQFGXBjJXo130_provenance.