Matches in Nanopublications for { <http://rdf.disgenet.org/nanopublications.trig#NP7408.RA7zj6HLkphTDYYITIXM0nXzl-hy_SwfB917YkHXQwrv8130_assertion> ?p ?o ?g. }
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- NP7408.RA7zj6HLkphTDYYITIXM0nXzl-hy_SwfB917YkHXQwrv8130_assertion type Assertion NP7408.RA7zj6HLkphTDYYITIXM0nXzl-hy_SwfB917YkHXQwrv8130_head.
- NP7408.RA7zj6HLkphTDYYITIXM0nXzl-hy_SwfB917YkHXQwrv8130_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." NP7408.RA7zj6HLkphTDYYITIXM0nXzl-hy_SwfB917YkHXQwrv8130_provenance.
- NP7408.RA7zj6HLkphTDYYITIXM0nXzl-hy_SwfB917YkHXQwrv8130_assertion evidence source_evidence_curated NP7408.RA7zj6HLkphTDYYITIXM0nXzl-hy_SwfB917YkHXQwrv8130_provenance.
- NP7408.RA7zj6HLkphTDYYITIXM0nXzl-hy_SwfB917YkHXQwrv8130_assertion SIO_000772 16116425 NP7408.RA7zj6HLkphTDYYITIXM0nXzl-hy_SwfB917YkHXQwrv8130_provenance.
- NP7408.RA7zj6HLkphTDYYITIXM0nXzl-hy_SwfB917YkHXQwrv8130_assertion wasDerivedFrom ctd_human-20130708 NP7408.RA7zj6HLkphTDYYITIXM0nXzl-hy_SwfB917YkHXQwrv8130_provenance.
- NP7408.RA7zj6HLkphTDYYITIXM0nXzl-hy_SwfB917YkHXQwrv8130_assertion wasGeneratedBy ECO_0000218 NP7408.RA7zj6HLkphTDYYITIXM0nXzl-hy_SwfB917YkHXQwrv8130_provenance.