Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP1247403.RA1oXH9VNFPnjGNyA6DEf2eLaEbIBHUsNCGFvdLT_roHw130_assertion> ?p ?o ?g. }
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- NP1247403.RA1oXH9VNFPnjGNyA6DEf2eLaEbIBHUsNCGFvdLT_roHw130_assertion type Assertion NP1247403.RA1oXH9VNFPnjGNyA6DEf2eLaEbIBHUsNCGFvdLT_roHw130_head.
- NP1247403.RA1oXH9VNFPnjGNyA6DEf2eLaEbIBHUsNCGFvdLT_roHw130_assertion description "[We observed that bilateral renal anomaly, renal cysts from unknown origin, a combination of two major renal anomalies and hypomagnesaemia were predictive for finding HNF1B mutations (P < 0.001; P < 0.001; P = 0.004; P = 0.008, respectively).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1247403.RA1oXH9VNFPnjGNyA6DEf2eLaEbIBHUsNCGFvdLT_roHw130_provenance.
- NP1247403.RA1oXH9VNFPnjGNyA6DEf2eLaEbIBHUsNCGFvdLT_roHw130_assertion evidence source_evidence_literature NP1247403.RA1oXH9VNFPnjGNyA6DEf2eLaEbIBHUsNCGFvdLT_roHw130_provenance.
- NP1247403.RA1oXH9VNFPnjGNyA6DEf2eLaEbIBHUsNCGFvdLT_roHw130_assertion SIO_000772 25500806 NP1247403.RA1oXH9VNFPnjGNyA6DEf2eLaEbIBHUsNCGFvdLT_roHw130_provenance.
- NP1247403.RA1oXH9VNFPnjGNyA6DEf2eLaEbIBHUsNCGFvdLT_roHw130_assertion wasDerivedFrom befree-2016 NP1247403.RA1oXH9VNFPnjGNyA6DEf2eLaEbIBHUsNCGFvdLT_roHw130_provenance.
- NP1247403.RA1oXH9VNFPnjGNyA6DEf2eLaEbIBHUsNCGFvdLT_roHw130_assertion wasGeneratedBy ECO_0000203 NP1247403.RA1oXH9VNFPnjGNyA6DEf2eLaEbIBHUsNCGFvdLT_roHw130_provenance.