Matches in Nanopublications for { <http://rdf.disgenet.org/nanopublications.trig#NP8070.RAG4WkiNDqMADe1WT_u95MPKy85a1dGu4z_D4sl9E6oj4130_assertion> ?p ?o ?g. }
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- NP8070.RAG4WkiNDqMADe1WT_u95MPKy85a1dGu4z_D4sl9E6oj4130_assertion type Assertion NP8070.RAG4WkiNDqMADe1WT_u95MPKy85a1dGu4z_D4sl9E6oj4130_head.
- NP8070.RAG4WkiNDqMADe1WT_u95MPKy85a1dGu4z_D4sl9E6oj4130_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." NP8070.RAG4WkiNDqMADe1WT_u95MPKy85a1dGu4z_D4sl9E6oj4130_provenance.
- NP8070.RAG4WkiNDqMADe1WT_u95MPKy85a1dGu4z_D4sl9E6oj4130_assertion evidence source_evidence_curated NP8070.RAG4WkiNDqMADe1WT_u95MPKy85a1dGu4z_D4sl9E6oj4130_provenance.
- NP8070.RAG4WkiNDqMADe1WT_u95MPKy85a1dGu4z_D4sl9E6oj4130_assertion SIO_000772 16116425 NP8070.RAG4WkiNDqMADe1WT_u95MPKy85a1dGu4z_D4sl9E6oj4130_provenance.
- NP8070.RAG4WkiNDqMADe1WT_u95MPKy85a1dGu4z_D4sl9E6oj4130_assertion wasDerivedFrom ctd_human-20130708 NP8070.RAG4WkiNDqMADe1WT_u95MPKy85a1dGu4z_D4sl9E6oj4130_provenance.
- NP8070.RAG4WkiNDqMADe1WT_u95MPKy85a1dGu4z_D4sl9E6oj4130_assertion wasGeneratedBy ECO_0000218 NP8070.RAG4WkiNDqMADe1WT_u95MPKy85a1dGu4z_D4sl9E6oj4130_provenance.