Matches in Nanopublications for { <http://rdf.disgenet.org/nanopublications.trig#NP248.RAEpWqtnUE6DSiGsVdY88fCfd3vEM5_8bKk5P6QEFU4zM130_assertion> ?p ?o ?g. }
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- NP248.RAEpWqtnUE6DSiGsVdY88fCfd3vEM5_8bKk5P6QEFU4zM130_assertion type Assertion NP248.RAEpWqtnUE6DSiGsVdY88fCfd3vEM5_8bKk5P6QEFU4zM130_head.
- NP248.RAEpWqtnUE6DSiGsVdY88fCfd3vEM5_8bKk5P6QEFU4zM130_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." NP248.RAEpWqtnUE6DSiGsVdY88fCfd3vEM5_8bKk5P6QEFU4zM130_provenance.
- NP248.RAEpWqtnUE6DSiGsVdY88fCfd3vEM5_8bKk5P6QEFU4zM130_assertion evidence source_evidence_curated NP248.RAEpWqtnUE6DSiGsVdY88fCfd3vEM5_8bKk5P6QEFU4zM130_provenance.
- NP248.RAEpWqtnUE6DSiGsVdY88fCfd3vEM5_8bKk5P6QEFU4zM130_assertion SIO_000772 16116425 NP248.RAEpWqtnUE6DSiGsVdY88fCfd3vEM5_8bKk5P6QEFU4zM130_provenance.
- NP248.RAEpWqtnUE6DSiGsVdY88fCfd3vEM5_8bKk5P6QEFU4zM130_assertion wasDerivedFrom uniprot-20130724 NP248.RAEpWqtnUE6DSiGsVdY88fCfd3vEM5_8bKk5P6QEFU4zM130_provenance.
- NP248.RAEpWqtnUE6DSiGsVdY88fCfd3vEM5_8bKk5P6QEFU4zM130_assertion wasGeneratedBy ECO_0000218 NP248.RAEpWqtnUE6DSiGsVdY88fCfd3vEM5_8bKk5P6QEFU4zM130_provenance.