Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP1247403.RA1oXH9VNFPnjGNyA6DEf2eLaEbIBHUsNCGFvdLT_roHw130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP1247403.RA1oXH9VNFPnjGNyA6DEf2eLaEbIBHUsNCGFvdLT_roHw130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP1247403.RA1oXH9VNFPnjGNyA6DEf2eLaEbIBHUsNCGFvdLT_roHw130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP1247403.RA1oXH9VNFPnjGNyA6DEf2eLaEbIBHUsNCGFvdLT_roHw130_provenance.
- 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.
- befree-2016 importedOn "2016-02-19" NP1247403.RA1oXH9VNFPnjGNyA6DEf2eLaEbIBHUsNCGFvdLT_roHw130_provenance.