Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP376945.RAgtgVhWO-wFG-HFuN-kqzZ-hDEvgEK9tTr0PoaUPGM0c130_assertion> ?p ?o ?g. }
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- NP376945.RAgtgVhWO-wFG-HFuN-kqzZ-hDEvgEK9tTr0PoaUPGM0c130_assertion type Assertion NP376945.RAgtgVhWO-wFG-HFuN-kqzZ-hDEvgEK9tTr0PoaUPGM0c130_head.
- NP376945.RAgtgVhWO-wFG-HFuN-kqzZ-hDEvgEK9tTr0PoaUPGM0c130_assertion description "[We postulate that mutation of UMOD disrupts the tertiary structure of UMOD and is responsible for the clinical changes of interstitial renal disease, polyuria, and hyperuricaemia found in MCKD2 and FJHN.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP376945.RAgtgVhWO-wFG-HFuN-kqzZ-hDEvgEK9tTr0PoaUPGM0c130_provenance.
- NP376945.RAgtgVhWO-wFG-HFuN-kqzZ-hDEvgEK9tTr0PoaUPGM0c130_assertion evidence source_evidence_literature NP376945.RAgtgVhWO-wFG-HFuN-kqzZ-hDEvgEK9tTr0PoaUPGM0c130_provenance.
- NP376945.RAgtgVhWO-wFG-HFuN-kqzZ-hDEvgEK9tTr0PoaUPGM0c130_assertion SIO_000772 12471200 NP376945.RAgtgVhWO-wFG-HFuN-kqzZ-hDEvgEK9tTr0PoaUPGM0c130_provenance.
- NP376945.RAgtgVhWO-wFG-HFuN-kqzZ-hDEvgEK9tTr0PoaUPGM0c130_assertion wasDerivedFrom befree-2016 NP376945.RAgtgVhWO-wFG-HFuN-kqzZ-hDEvgEK9tTr0PoaUPGM0c130_provenance.
- NP376945.RAgtgVhWO-wFG-HFuN-kqzZ-hDEvgEK9tTr0PoaUPGM0c130_assertion wasGeneratedBy ECO_0000203 NP376945.RAgtgVhWO-wFG-HFuN-kqzZ-hDEvgEK9tTr0PoaUPGM0c130_provenance.