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- source_evidence_literature type ECO_0000212 NP766692.RA0Bmz5ixC7ZWC-YWe9pWZNzWvEV2eXO-gRWYJOnmeiVQ130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP766692.RA0Bmz5ixC7ZWC-YWe9pWZNzWvEV2eXO-gRWYJOnmeiVQ130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP766692.RA0Bmz5ixC7ZWC-YWe9pWZNzWvEV2eXO-gRWYJOnmeiVQ130_provenance.
- NP766692.RA0Bmz5ixC7ZWC-YWe9pWZNzWvEV2eXO-gRWYJOnmeiVQ130_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." NP766692.RA0Bmz5ixC7ZWC-YWe9pWZNzWvEV2eXO-gRWYJOnmeiVQ130_provenance.
- NP766692.RA0Bmz5ixC7ZWC-YWe9pWZNzWvEV2eXO-gRWYJOnmeiVQ130_assertion evidence source_evidence_literature NP766692.RA0Bmz5ixC7ZWC-YWe9pWZNzWvEV2eXO-gRWYJOnmeiVQ130_provenance.
- NP766692.RA0Bmz5ixC7ZWC-YWe9pWZNzWvEV2eXO-gRWYJOnmeiVQ130_assertion SIO_000772 12471200 NP766692.RA0Bmz5ixC7ZWC-YWe9pWZNzWvEV2eXO-gRWYJOnmeiVQ130_provenance.
- NP766692.RA0Bmz5ixC7ZWC-YWe9pWZNzWvEV2eXO-gRWYJOnmeiVQ130_assertion wasDerivedFrom befree-20150227 NP766692.RA0Bmz5ixC7ZWC-YWe9pWZNzWvEV2eXO-gRWYJOnmeiVQ130_provenance.
- NP766692.RA0Bmz5ixC7ZWC-YWe9pWZNzWvEV2eXO-gRWYJOnmeiVQ130_assertion wasGeneratedBy ECO_0000203 NP766692.RA0Bmz5ixC7ZWC-YWe9pWZNzWvEV2eXO-gRWYJOnmeiVQ130_provenance.
- befree-20150227 importedOn "2015-02-27" NP766692.RA0Bmz5ixC7ZWC-YWe9pWZNzWvEV2eXO-gRWYJOnmeiVQ130_provenance.