Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP6274.RACTpKrKAr96G5ModN6RMedIY5aK3562jEALiQovuBIo4130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_curated type ECO_0000205 NP6274.RACTpKrKAr96G5ModN6RMedIY5aK3562jEALiQovuBIo4130_provenance.
- source_evidence_curated label "DisGeNET evidence - CURATED" NP6274.RACTpKrKAr96G5ModN6RMedIY5aK3562jEALiQovuBIo4130_provenance.
- source_evidence_curated comment "Gene-disease associations manually curated." NP6274.RACTpKrKAr96G5ModN6RMedIY5aK3562jEALiQovuBIo4130_provenance.
- NP6274.RACTpKrKAr96G5ModN6RMedIY5aK3562jEALiQovuBIo4130_assertion description "[We studied 11 individuals with renal tubular dysgenesis, belonging to nine families, and found that they had homozygous or compound heterozygous mutations in the genes encoding renin, angiotensinogen, angiotensin converting enzyme or angiotensin II receptor type 1.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP6274.RACTpKrKAr96G5ModN6RMedIY5aK3562jEALiQovuBIo4130_provenance.
- NP6274.RACTpKrKAr96G5ModN6RMedIY5aK3562jEALiQovuBIo4130_assertion evidence source_evidence_curated NP6274.RACTpKrKAr96G5ModN6RMedIY5aK3562jEALiQovuBIo4130_provenance.
- NP6274.RACTpKrKAr96G5ModN6RMedIY5aK3562jEALiQovuBIo4130_assertion SIO_000772 16116425 NP6274.RACTpKrKAr96G5ModN6RMedIY5aK3562jEALiQovuBIo4130_provenance.
- NP6274.RACTpKrKAr96G5ModN6RMedIY5aK3562jEALiQovuBIo4130_assertion wasDerivedFrom ctd_human-20150221 NP6274.RACTpKrKAr96G5ModN6RMedIY5aK3562jEALiQovuBIo4130_provenance.
- NP6274.RACTpKrKAr96G5ModN6RMedIY5aK3562jEALiQovuBIo4130_assertion wasGeneratedBy ECO_0000218 NP6274.RACTpKrKAr96G5ModN6RMedIY5aK3562jEALiQovuBIo4130_provenance.
- ctd_human-20150221 importedOn "2015-02-21" NP6274.RACTpKrKAr96G5ModN6RMedIY5aK3562jEALiQovuBIo4130_provenance.