Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP1064762.RAyX7g_Rwappzmg-8RiX62VtoYwtoaA_f4oydBIOizsbI130_assertion> ?p ?o ?g. }
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- NP1064762.RAyX7g_Rwappzmg-8RiX62VtoYwtoaA_f4oydBIOizsbI130_assertion type Assertion NP1064762.RAyX7g_Rwappzmg-8RiX62VtoYwtoaA_f4oydBIOizsbI130_head.
- NP1064762.RAyX7g_Rwappzmg-8RiX62VtoYwtoaA_f4oydBIOizsbI130_assertion wasGeneratedBy ECO_0000203 NP1064762.RAyX7g_Rwappzmg-8RiX62VtoYwtoaA_f4oydBIOizsbI130_provenance.
- NP1064762.RAyX7g_Rwappzmg-8RiX62VtoYwtoaA_f4oydBIOizsbI130_assertion wasDerivedFrom befree-2016 NP1064762.RAyX7g_Rwappzmg-8RiX62VtoYwtoaA_f4oydBIOizsbI130_provenance.
- NP1064762.RAyX7g_Rwappzmg-8RiX62VtoYwtoaA_f4oydBIOizsbI130_assertion SIO_000772 23539225 NP1064762.RAyX7g_Rwappzmg-8RiX62VtoYwtoaA_f4oydBIOizsbI130_provenance.
- NP1064762.RAyX7g_Rwappzmg-8RiX62VtoYwtoaA_f4oydBIOizsbI130_assertion evidence source_evidence_literature NP1064762.RAyX7g_Rwappzmg-8RiX62VtoYwtoaA_f4oydBIOizsbI130_provenance.
- NP1064762.RAyX7g_Rwappzmg-8RiX62VtoYwtoaA_f4oydBIOizsbI130_assertion description "[This study reports the screening of two genes (HNF1B and PAX2) involved in monogenic syndromic CAKUT in a cohort of 103 fetuses from 91 families with very severe CAKUT that appeared isolated by fetal ultrasound examination and led to termination of pregnancy.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1064762.RAyX7g_Rwappzmg-8RiX62VtoYwtoaA_f4oydBIOizsbI130_provenance.