Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP1327026.RAxhcfUMjDGgXp-MTrjf42t-igGRrp2-cuHnLZZLCtNWU130_assertion> ?p ?o ?g. }
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- NP1327026.RAxhcfUMjDGgXp-MTrjf42t-igGRrp2-cuHnLZZLCtNWU130_assertion type Assertion NP1327026.RAxhcfUMjDGgXp-MTrjf42t-igGRrp2-cuHnLZZLCtNWU130_head.
- NP1327026.RAxhcfUMjDGgXp-MTrjf42t-igGRrp2-cuHnLZZLCtNWU130_assertion description "[In autosomal dominant polycystic kidney disease 1) the genetic localization of the defective gene that causes type 1 disease has been narrowed to 500 to 750 kb on chromosome 16; 2) cystogenesis has been associated with increased cell proliferation, continuing cyst secretion, and a defect in cell polarity; however, the mechanisms by which the genetic defects in autosomal dominant polycystic kidney disease translate into cyst formation are unknown; 3) activation of the renin system has been reported as an important potential cause of hypertension; and 4) factors that influence the progression to renal failure have been identified.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1327026.RAxhcfUMjDGgXp-MTrjf42t-igGRrp2-cuHnLZZLCtNWU130_provenance.
- NP1327026.RAxhcfUMjDGgXp-MTrjf42t-igGRrp2-cuHnLZZLCtNWU130_assertion evidence source_evidence_literature NP1327026.RAxhcfUMjDGgXp-MTrjf42t-igGRrp2-cuHnLZZLCtNWU130_provenance.
- NP1327026.RAxhcfUMjDGgXp-MTrjf42t-igGRrp2-cuHnLZZLCtNWU130_assertion SIO_000772 7922177 NP1327026.RAxhcfUMjDGgXp-MTrjf42t-igGRrp2-cuHnLZZLCtNWU130_provenance.
- NP1327026.RAxhcfUMjDGgXp-MTrjf42t-igGRrp2-cuHnLZZLCtNWU130_assertion wasDerivedFrom befree-2016 NP1327026.RAxhcfUMjDGgXp-MTrjf42t-igGRrp2-cuHnLZZLCtNWU130_provenance.
- NP1327026.RAxhcfUMjDGgXp-MTrjf42t-igGRrp2-cuHnLZZLCtNWU130_assertion wasGeneratedBy ECO_0000203 NP1327026.RAxhcfUMjDGgXp-MTrjf42t-igGRrp2-cuHnLZZLCtNWU130_provenance.