Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP528764.RA0VeisrOnyXX3-BVmEevOA3W8MenqHyUJ2PZUa9QbZq0130_assertion> ?p ?o ?g. }
Showing items 1 to 6 of
6
with 100 items per page.
- NP528764.RA0VeisrOnyXX3-BVmEevOA3W8MenqHyUJ2PZUa9QbZq0130_assertion type Assertion NP528764.RA0VeisrOnyXX3-BVmEevOA3W8MenqHyUJ2PZUa9QbZq0130_head.
- NP528764.RA0VeisrOnyXX3-BVmEevOA3W8MenqHyUJ2PZUa9QbZq0130_assertion description "[The basic molecular work-up included analysis of concordance based on 10 polymorphic markers (D3S1358, vVA, FGA, amelogenin, D8S1179, D21S11, D18S51, D5S818, D13S317, D7S820) and exclusion of the major slit-diaphragm gene mutation (NPHS2, CD2AP, WT1) causing nephrotic syndrome.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP528764.RA0VeisrOnyXX3-BVmEevOA3W8MenqHyUJ2PZUa9QbZq0130_provenance.
- NP528764.RA0VeisrOnyXX3-BVmEevOA3W8MenqHyUJ2PZUa9QbZq0130_assertion evidence source_evidence_literature NP528764.RA0VeisrOnyXX3-BVmEevOA3W8MenqHyUJ2PZUa9QbZq0130_provenance.
- NP528764.RA0VeisrOnyXX3-BVmEevOA3W8MenqHyUJ2PZUa9QbZq0130_assertion SIO_000772 16382323 NP528764.RA0VeisrOnyXX3-BVmEevOA3W8MenqHyUJ2PZUa9QbZq0130_provenance.
- NP528764.RA0VeisrOnyXX3-BVmEevOA3W8MenqHyUJ2PZUa9QbZq0130_assertion wasDerivedFrom befree-2016 NP528764.RA0VeisrOnyXX3-BVmEevOA3W8MenqHyUJ2PZUa9QbZq0130_provenance.
- NP528764.RA0VeisrOnyXX3-BVmEevOA3W8MenqHyUJ2PZUa9QbZq0130_assertion wasGeneratedBy ECO_0000203 NP528764.RA0VeisrOnyXX3-BVmEevOA3W8MenqHyUJ2PZUa9QbZq0130_provenance.