Matches in Nanopublications for { <http://rdf.disgenet.org/nanopublications.trig#NP754090.RAJhmEqP7jg476XcsYbN6VeWCSEThrKtA5R-XUd_ViLIs130_assertion> ?p ?o ?g. }
Showing items 1 to 6 of
6
with 100 items per page.
- NP754090.RAJhmEqP7jg476XcsYbN6VeWCSEThrKtA5R-XUd_ViLIs130_assertion type Assertion NP754090.RAJhmEqP7jg476XcsYbN6VeWCSEThrKtA5R-XUd_ViLIs130_head.
- NP754090.RAJhmEqP7jg476XcsYbN6VeWCSEThrKtA5R-XUd_ViLIs130_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." NP754090.RAJhmEqP7jg476XcsYbN6VeWCSEThrKtA5R-XUd_ViLIs130_provenance.
- NP754090.RAJhmEqP7jg476XcsYbN6VeWCSEThrKtA5R-XUd_ViLIs130_assertion evidence source_evidence_literature NP754090.RAJhmEqP7jg476XcsYbN6VeWCSEThrKtA5R-XUd_ViLIs130_provenance.
- NP754090.RAJhmEqP7jg476XcsYbN6VeWCSEThrKtA5R-XUd_ViLIs130_assertion SIO_000772 16382323 NP754090.RAJhmEqP7jg476XcsYbN6VeWCSEThrKtA5R-XUd_ViLIs130_provenance.
- NP754090.RAJhmEqP7jg476XcsYbN6VeWCSEThrKtA5R-XUd_ViLIs130_assertion wasDerivedFrom befree-20140225 NP754090.RAJhmEqP7jg476XcsYbN6VeWCSEThrKtA5R-XUd_ViLIs130_provenance.
- NP754090.RAJhmEqP7jg476XcsYbN6VeWCSEThrKtA5R-XUd_ViLIs130_assertion wasGeneratedBy ECO_0000203 NP754090.RAJhmEqP7jg476XcsYbN6VeWCSEThrKtA5R-XUd_ViLIs130_provenance.