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- NP806363.RA2st4QIKmS80awxoLcnQIuR0Wn_jE-9ivge-_GiyqpT4130_assertion type Assertion NP806363.RA2st4QIKmS80awxoLcnQIuR0Wn_jE-9ivge-_GiyqpT4130_head.
- NP806363.RA2st4QIKmS80awxoLcnQIuR0Wn_jE-9ivge-_GiyqpT4130_assertion description "[Loss-of-function mutations in TRPM6 are a molecular cause of hypomagnesemia with secondary hypocalcemia, suggesting that TRPM6 is critically involved in transcellular Mg2+ transport in the kidney.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP806363.RA2st4QIKmS80awxoLcnQIuR0Wn_jE-9ivge-_GiyqpT4130_provenance.
- NP806363.RA2st4QIKmS80awxoLcnQIuR0Wn_jE-9ivge-_GiyqpT4130_assertion evidence source_evidence_literature NP806363.RA2st4QIKmS80awxoLcnQIuR0Wn_jE-9ivge-_GiyqpT4130_provenance.
- NP806363.RA2st4QIKmS80awxoLcnQIuR0Wn_jE-9ivge-_GiyqpT4130_assertion SIO_000772 20395377 NP806363.RA2st4QIKmS80awxoLcnQIuR0Wn_jE-9ivge-_GiyqpT4130_provenance.
- NP806363.RA2st4QIKmS80awxoLcnQIuR0Wn_jE-9ivge-_GiyqpT4130_assertion wasDerivedFrom befree-2016 NP806363.RA2st4QIKmS80awxoLcnQIuR0Wn_jE-9ivge-_GiyqpT4130_provenance.
- NP806363.RA2st4QIKmS80awxoLcnQIuR0Wn_jE-9ivge-_GiyqpT4130_assertion wasGeneratedBy ECO_0000203 NP806363.RA2st4QIKmS80awxoLcnQIuR0Wn_jE-9ivge-_GiyqpT4130_provenance.