Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP148983.RATWpdrktlO93dwOAPvhMn3Iav-vHdlpuQGLMLoWi7eck130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP148983.RATWpdrktlO93dwOAPvhMn3Iav-vHdlpuQGLMLoWi7eck130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP148983.RATWpdrktlO93dwOAPvhMn3Iav-vHdlpuQGLMLoWi7eck130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP148983.RATWpdrktlO93dwOAPvhMn3Iav-vHdlpuQGLMLoWi7eck130_provenance.
- NP148983.RATWpdrktlO93dwOAPvhMn3Iav-vHdlpuQGLMLoWi7eck130_assertion description "[Deletion of two closely related genes, complement factor H-related 1 (CFHR1) and complement factor H-related 3 (CFHR3), increases the risk of atypical hemolytic uremic syndrome.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP148983.RATWpdrktlO93dwOAPvhMn3Iav-vHdlpuQGLMLoWi7eck130_provenance.
- NP148983.RATWpdrktlO93dwOAPvhMn3Iav-vHdlpuQGLMLoWi7eck130_assertion evidence source_evidence_literature NP148983.RATWpdrktlO93dwOAPvhMn3Iav-vHdlpuQGLMLoWi7eck130_provenance.
- NP148983.RATWpdrktlO93dwOAPvhMn3Iav-vHdlpuQGLMLoWi7eck130_assertion SIO_000772 17367211 NP148983.RATWpdrktlO93dwOAPvhMn3Iav-vHdlpuQGLMLoWi7eck130_provenance.
- NP148983.RATWpdrktlO93dwOAPvhMn3Iav-vHdlpuQGLMLoWi7eck130_assertion wasDerivedFrom lhgdn-20090331 NP148983.RATWpdrktlO93dwOAPvhMn3Iav-vHdlpuQGLMLoWi7eck130_provenance.
- NP148983.RATWpdrktlO93dwOAPvhMn3Iav-vHdlpuQGLMLoWi7eck130_assertion wasGeneratedBy ECO_0000203 NP148983.RATWpdrktlO93dwOAPvhMn3Iav-vHdlpuQGLMLoWi7eck130_provenance.
- lhgdn-20090331 importedOn "2009-03-31" NP148983.RATWpdrktlO93dwOAPvhMn3Iav-vHdlpuQGLMLoWi7eck130_provenance.