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- source_evidence_literature type ECO_0000212 NP973811.RAaYUIffhmBN2R2BCMgj9KegQLzUOCTgYr5dt0xTbhVVU130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP973811.RAaYUIffhmBN2R2BCMgj9KegQLzUOCTgYr5dt0xTbhVVU130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP973811.RAaYUIffhmBN2R2BCMgj9KegQLzUOCTgYr5dt0xTbhVVU130_provenance.
- NP973811.RAaYUIffhmBN2R2BCMgj9KegQLzUOCTgYr5dt0xTbhVVU130_assertion description "[Hereditary hypophosphatemic rickets with hypercalciuria is a rare metabolic disorder associated with mutations in SLC34A3, the gene that encodes the renal sodium phosphate cotransporter NaPi-IIc.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP973811.RAaYUIffhmBN2R2BCMgj9KegQLzUOCTgYr5dt0xTbhVVU130_provenance.
- NP973811.RAaYUIffhmBN2R2BCMgj9KegQLzUOCTgYr5dt0xTbhVVU130_assertion evidence source_evidence_literature NP973811.RAaYUIffhmBN2R2BCMgj9KegQLzUOCTgYr5dt0xTbhVVU130_provenance.
- NP973811.RAaYUIffhmBN2R2BCMgj9KegQLzUOCTgYr5dt0xTbhVVU130_assertion SIO_000772 18996815 NP973811.RAaYUIffhmBN2R2BCMgj9KegQLzUOCTgYr5dt0xTbhVVU130_provenance.
- NP973811.RAaYUIffhmBN2R2BCMgj9KegQLzUOCTgYr5dt0xTbhVVU130_assertion wasDerivedFrom befree-20150227 NP973811.RAaYUIffhmBN2R2BCMgj9KegQLzUOCTgYr5dt0xTbhVVU130_provenance.
- NP973811.RAaYUIffhmBN2R2BCMgj9KegQLzUOCTgYr5dt0xTbhVVU130_assertion wasGeneratedBy ECO_0000203 NP973811.RAaYUIffhmBN2R2BCMgj9KegQLzUOCTgYr5dt0xTbhVVU130_provenance.
- befree-20150227 importedOn "2015-02-27" NP973811.RAaYUIffhmBN2R2BCMgj9KegQLzUOCTgYr5dt0xTbhVVU130_provenance.