Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP828454.RAeeS2DrsrV-Q5ul15w9HH8h5tEhf9nGNszdymreHqEcA130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP828454.RAeeS2DrsrV-Q5ul15w9HH8h5tEhf9nGNszdymreHqEcA130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP828454.RAeeS2DrsrV-Q5ul15w9HH8h5tEhf9nGNszdymreHqEcA130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP828454.RAeeS2DrsrV-Q5ul15w9HH8h5tEhf9nGNszdymreHqEcA130_provenance.
- NP828454.RAeeS2DrsrV-Q5ul15w9HH8h5tEhf9nGNszdymreHqEcA130_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." NP828454.RAeeS2DrsrV-Q5ul15w9HH8h5tEhf9nGNszdymreHqEcA130_provenance.
- NP828454.RAeeS2DrsrV-Q5ul15w9HH8h5tEhf9nGNszdymreHqEcA130_assertion evidence source_evidence_literature NP828454.RAeeS2DrsrV-Q5ul15w9HH8h5tEhf9nGNszdymreHqEcA130_provenance.
- NP828454.RAeeS2DrsrV-Q5ul15w9HH8h5tEhf9nGNszdymreHqEcA130_assertion SIO_000772 20395377 NP828454.RAeeS2DrsrV-Q5ul15w9HH8h5tEhf9nGNszdymreHqEcA130_provenance.
- NP828454.RAeeS2DrsrV-Q5ul15w9HH8h5tEhf9nGNszdymreHqEcA130_assertion wasDerivedFrom befree-20140225 NP828454.RAeeS2DrsrV-Q5ul15w9HH8h5tEhf9nGNszdymreHqEcA130_provenance.
- NP828454.RAeeS2DrsrV-Q5ul15w9HH8h5tEhf9nGNszdymreHqEcA130_assertion wasGeneratedBy ECO_0000203 NP828454.RAeeS2DrsrV-Q5ul15w9HH8h5tEhf9nGNszdymreHqEcA130_provenance.
- befree-20140225 importedOn "2014-02-25" NP828454.RAeeS2DrsrV-Q5ul15w9HH8h5tEhf9nGNszdymreHqEcA130_provenance.