Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP725176.RAXYF6flfFdp972eRTToj1-EsUWsQnBEZx_IMpfyu5buc130_assertion> ?p ?o ?g. }
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- NP725176.RAXYF6flfFdp972eRTToj1-EsUWsQnBEZx_IMpfyu5buc130_assertion type Assertion NP725176.RAXYF6flfFdp972eRTToj1-EsUWsQnBEZx_IMpfyu5buc130_head.
- NP725176.RAXYF6flfFdp972eRTToj1-EsUWsQnBEZx_IMpfyu5buc130_assertion wasGeneratedBy ECO_0000203 NP725176.RAXYF6flfFdp972eRTToj1-EsUWsQnBEZx_IMpfyu5buc130_provenance.
- NP725176.RAXYF6flfFdp972eRTToj1-EsUWsQnBEZx_IMpfyu5buc130_assertion wasDerivedFrom befree-20150227 NP725176.RAXYF6flfFdp972eRTToj1-EsUWsQnBEZx_IMpfyu5buc130_provenance.
- NP725176.RAXYF6flfFdp972eRTToj1-EsUWsQnBEZx_IMpfyu5buc130_assertion SIO_000772 23539225 NP725176.RAXYF6flfFdp972eRTToj1-EsUWsQnBEZx_IMpfyu5buc130_provenance.
- NP725176.RAXYF6flfFdp972eRTToj1-EsUWsQnBEZx_IMpfyu5buc130_assertion evidence source_evidence_literature NP725176.RAXYF6flfFdp972eRTToj1-EsUWsQnBEZx_IMpfyu5buc130_provenance.
- NP725176.RAXYF6flfFdp972eRTToj1-EsUWsQnBEZx_IMpfyu5buc130_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." NP725176.RAXYF6flfFdp972eRTToj1-EsUWsQnBEZx_IMpfyu5buc130_provenance.