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- source_evidence_literature type ECO_0000212 NP256338.RAUjx7Dgje1CC9Wz9iP3oAie_DxWLnck-MgGj_nrJGKa4130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP256338.RAUjx7Dgje1CC9Wz9iP3oAie_DxWLnck-MgGj_nrJGKa4130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP256338.RAUjx7Dgje1CC9Wz9iP3oAie_DxWLnck-MgGj_nrJGKa4130_provenance.
- NP256338.RAUjx7Dgje1CC9Wz9iP3oAie_DxWLnck-MgGj_nrJGKa4130_assertion description "[Overall, our findings establish PCBD1 as a coactivator of the HNF1B-mediated transcription necessary for fine tuning FXYD2 transcription in the DCT and suggest that patients with HPABH4D should be monitored for previously unrecognized late complications, such as hypomagnesemia and MODY diabetes.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP256338.RAUjx7Dgje1CC9Wz9iP3oAie_DxWLnck-MgGj_nrJGKa4130_provenance.
- NP256338.RAUjx7Dgje1CC9Wz9iP3oAie_DxWLnck-MgGj_nrJGKa4130_assertion evidence source_evidence_literature NP256338.RAUjx7Dgje1CC9Wz9iP3oAie_DxWLnck-MgGj_nrJGKa4130_provenance.
- NP256338.RAUjx7Dgje1CC9Wz9iP3oAie_DxWLnck-MgGj_nrJGKa4130_assertion SIO_000772 24204001 NP256338.RAUjx7Dgje1CC9Wz9iP3oAie_DxWLnck-MgGj_nrJGKa4130_provenance.
- NP256338.RAUjx7Dgje1CC9Wz9iP3oAie_DxWLnck-MgGj_nrJGKa4130_assertion wasDerivedFrom befree-20150227 NP256338.RAUjx7Dgje1CC9Wz9iP3oAie_DxWLnck-MgGj_nrJGKa4130_provenance.
- NP256338.RAUjx7Dgje1CC9Wz9iP3oAie_DxWLnck-MgGj_nrJGKa4130_assertion wasGeneratedBy ECO_0000203 NP256338.RAUjx7Dgje1CC9Wz9iP3oAie_DxWLnck-MgGj_nrJGKa4130_provenance.
- befree-20150227 importedOn "2015-02-27" NP256338.RAUjx7Dgje1CC9Wz9iP3oAie_DxWLnck-MgGj_nrJGKa4130_provenance.