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- source_evidence_literature type ECO_0000212 NP916867.RAauj061HaOQIU5iay-TnWD2apoWz44NafhGf9ejleeow130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP916867.RAauj061HaOQIU5iay-TnWD2apoWz44NafhGf9ejleeow130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP916867.RAauj061HaOQIU5iay-TnWD2apoWz44NafhGf9ejleeow130_provenance.
- NP916867.RAauj061HaOQIU5iay-TnWD2apoWz44NafhGf9ejleeow130_assertion description "[Gain-of-function mutations in TRPC6 cause hereditary focal segmental glomerulosclerosis (FSGS), and several human acquired proteinuric diseases show increased glomerular TRPC6 expression.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP916867.RAauj061HaOQIU5iay-TnWD2apoWz44NafhGf9ejleeow130_provenance.
- NP916867.RAauj061HaOQIU5iay-TnWD2apoWz44NafhGf9ejleeow130_assertion evidence source_evidence_literature NP916867.RAauj061HaOQIU5iay-TnWD2apoWz44NafhGf9ejleeow130_provenance.
- NP916867.RAauj061HaOQIU5iay-TnWD2apoWz44NafhGf9ejleeow130_assertion SIO_000772 21839714 NP916867.RAauj061HaOQIU5iay-TnWD2apoWz44NafhGf9ejleeow130_provenance.
- NP916867.RAauj061HaOQIU5iay-TnWD2apoWz44NafhGf9ejleeow130_assertion wasDerivedFrom befree-2016 NP916867.RAauj061HaOQIU5iay-TnWD2apoWz44NafhGf9ejleeow130_provenance.
- NP916867.RAauj061HaOQIU5iay-TnWD2apoWz44NafhGf9ejleeow130_assertion wasGeneratedBy ECO_0000203 NP916867.RAauj061HaOQIU5iay-TnWD2apoWz44NafhGf9ejleeow130_provenance.
- befree-2016 importedOn "2016-02-19" NP916867.RAauj061HaOQIU5iay-TnWD2apoWz44NafhGf9ejleeow130_provenance.