Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP709154.RAmuMRjyAdSSIvufUvQ0I0XGk8jWQg8FURZnVITH3MLi0130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP709154.RAmuMRjyAdSSIvufUvQ0I0XGk8jWQg8FURZnVITH3MLi0130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP709154.RAmuMRjyAdSSIvufUvQ0I0XGk8jWQg8FURZnVITH3MLi0130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP709154.RAmuMRjyAdSSIvufUvQ0I0XGk8jWQg8FURZnVITH3MLi0130_provenance.
- NP709154.RAmuMRjyAdSSIvufUvQ0I0XGk8jWQg8FURZnVITH3MLi0130_assertion description "[We describe a patient with a novel frameshift mutation (c.1880_1881insA) in the JAG1 gene who presented with chronic renal failure and hypertension but without evidence of renal vascular or aortic stenosis.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP709154.RAmuMRjyAdSSIvufUvQ0I0XGk8jWQg8FURZnVITH3MLi0130_provenance.
- NP709154.RAmuMRjyAdSSIvufUvQ0I0XGk8jWQg8FURZnVITH3MLi0130_assertion evidence source_evidence_literature NP709154.RAmuMRjyAdSSIvufUvQ0I0XGk8jWQg8FURZnVITH3MLi0130_provenance.
- NP709154.RAmuMRjyAdSSIvufUvQ0I0XGk8jWQg8FURZnVITH3MLi0130_assertion SIO_000772 16013021 NP709154.RAmuMRjyAdSSIvufUvQ0I0XGk8jWQg8FURZnVITH3MLi0130_provenance.
- NP709154.RAmuMRjyAdSSIvufUvQ0I0XGk8jWQg8FURZnVITH3MLi0130_assertion wasDerivedFrom befree-20140225 NP709154.RAmuMRjyAdSSIvufUvQ0I0XGk8jWQg8FURZnVITH3MLi0130_provenance.
- NP709154.RAmuMRjyAdSSIvufUvQ0I0XGk8jWQg8FURZnVITH3MLi0130_assertion wasGeneratedBy ECO_0000203 NP709154.RAmuMRjyAdSSIvufUvQ0I0XGk8jWQg8FURZnVITH3MLi0130_provenance.
- befree-20140225 importedOn "2014-02-25" NP709154.RAmuMRjyAdSSIvufUvQ0I0XGk8jWQg8FURZnVITH3MLi0130_provenance.