Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP43016.RAhjF57apo64p8day6Jc3fuLvoKunPyhLvi_EveYXrd5c130_provenance>. }
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- source_evidence_predicted type ECO_0000266 NP43016.RAhjF57apo64p8day6Jc3fuLvoKunPyhLvi_EveYXrd5c130_provenance.
- source_evidence_predicted label "DisGeNET evidence - PREDICTED" NP43016.RAhjF57apo64p8day6Jc3fuLvoKunPyhLvi_EveYXrd5c130_provenance.
- source_evidence_predicted comment "Gene-disease associations inferred from animal model manually asserted gene-disease associations." NP43016.RAhjF57apo64p8day6Jc3fuLvoKunPyhLvi_EveYXrd5c130_provenance.
- NP43016.RAhjF57apo64p8day6Jc3fuLvoKunPyhLvi_EveYXrd5c130_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." NP43016.RAhjF57apo64p8day6Jc3fuLvoKunPyhLvi_EveYXrd5c130_provenance.
- NP43016.RAhjF57apo64p8day6Jc3fuLvoKunPyhLvi_EveYXrd5c130_assertion evidence source_evidence_predicted NP43016.RAhjF57apo64p8day6Jc3fuLvoKunPyhLvi_EveYXrd5c130_provenance.
- NP43016.RAhjF57apo64p8day6Jc3fuLvoKunPyhLvi_EveYXrd5c130_assertion SIO_000772 21839714 NP43016.RAhjF57apo64p8day6Jc3fuLvoKunPyhLvi_EveYXrd5c130_provenance.
- NP43016.RAhjF57apo64p8day6Jc3fuLvoKunPyhLvi_EveYXrd5c130_assertion wasDerivedFrom rgd-20150221 NP43016.RAhjF57apo64p8day6Jc3fuLvoKunPyhLvi_EveYXrd5c130_provenance.
- NP43016.RAhjF57apo64p8day6Jc3fuLvoKunPyhLvi_EveYXrd5c130_assertion wasGeneratedBy ECO_0000218 NP43016.RAhjF57apo64p8day6Jc3fuLvoKunPyhLvi_EveYXrd5c130_provenance.
- rgd-20150221 importedOn "2015-02-21" NP43016.RAhjF57apo64p8day6Jc3fuLvoKunPyhLvi_EveYXrd5c130_provenance.