Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP15832.RASGNayJnkAB9RsnwAImfR25YTYhpSdGa6DW2GxM1fJh4130_assertion> ?p ?o ?g. }
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- NP15832.RASGNayJnkAB9RsnwAImfR25YTYhpSdGa6DW2GxM1fJh4130_assertion type Assertion NP15832.RASGNayJnkAB9RsnwAImfR25YTYhpSdGa6DW2GxM1fJh4130_head.
- NP15832.RASGNayJnkAB9RsnwAImfR25YTYhpSdGa6DW2GxM1fJh4130_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." NP15832.RASGNayJnkAB9RsnwAImfR25YTYhpSdGa6DW2GxM1fJh4130_provenance.
- NP15832.RASGNayJnkAB9RsnwAImfR25YTYhpSdGa6DW2GxM1fJh4130_assertion evidence source_evidence_curated NP15832.RASGNayJnkAB9RsnwAImfR25YTYhpSdGa6DW2GxM1fJh4130_provenance.
- NP15832.RASGNayJnkAB9RsnwAImfR25YTYhpSdGa6DW2GxM1fJh4130_assertion SIO_000772 16116425 NP15832.RASGNayJnkAB9RsnwAImfR25YTYhpSdGa6DW2GxM1fJh4130_provenance.
- NP15832.RASGNayJnkAB9RsnwAImfR25YTYhpSdGa6DW2GxM1fJh4130_assertion wasDerivedFrom ctd_human-2016 NP15832.RASGNayJnkAB9RsnwAImfR25YTYhpSdGa6DW2GxM1fJh4130_provenance.
- NP15832.RASGNayJnkAB9RsnwAImfR25YTYhpSdGa6DW2GxM1fJh4130_assertion wasGeneratedBy ECO_0000218 NP15832.RASGNayJnkAB9RsnwAImfR25YTYhpSdGa6DW2GxM1fJh4130_provenance.