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- source_evidence_literature type ECO_0000212 NP794947.RA9heLZIEQIul8lHGD7SSMCOsB1JAT3Cm83e-gxPjbLPQ130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP794947.RA9heLZIEQIul8lHGD7SSMCOsB1JAT3Cm83e-gxPjbLPQ130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP794947.RA9heLZIEQIul8lHGD7SSMCOsB1JAT3Cm83e-gxPjbLPQ130_provenance.
- NP794947.RA9heLZIEQIul8lHGD7SSMCOsB1JAT3Cm83e-gxPjbLPQ130_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." NP794947.RA9heLZIEQIul8lHGD7SSMCOsB1JAT3Cm83e-gxPjbLPQ130_provenance.
- NP794947.RA9heLZIEQIul8lHGD7SSMCOsB1JAT3Cm83e-gxPjbLPQ130_assertion evidence source_evidence_literature NP794947.RA9heLZIEQIul8lHGD7SSMCOsB1JAT3Cm83e-gxPjbLPQ130_provenance.
- NP794947.RA9heLZIEQIul8lHGD7SSMCOsB1JAT3Cm83e-gxPjbLPQ130_assertion SIO_000772 19389850 NP794947.RA9heLZIEQIul8lHGD7SSMCOsB1JAT3Cm83e-gxPjbLPQ130_provenance.
- NP794947.RA9heLZIEQIul8lHGD7SSMCOsB1JAT3Cm83e-gxPjbLPQ130_assertion wasDerivedFrom befree-20140225 NP794947.RA9heLZIEQIul8lHGD7SSMCOsB1JAT3Cm83e-gxPjbLPQ130_provenance.
- NP794947.RA9heLZIEQIul8lHGD7SSMCOsB1JAT3Cm83e-gxPjbLPQ130_assertion wasGeneratedBy ECO_0000203 NP794947.RA9heLZIEQIul8lHGD7SSMCOsB1JAT3Cm83e-gxPjbLPQ130_provenance.
- befree-20140225 importedOn "2014-02-25" NP794947.RA9heLZIEQIul8lHGD7SSMCOsB1JAT3Cm83e-gxPjbLPQ130_provenance.