Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP530812.RAQO8QUmXsafzJV5drNpXRiEaN6knA06tWQLMcS1HqaH8130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP530812.RAQO8QUmXsafzJV5drNpXRiEaN6knA06tWQLMcS1HqaH8130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP530812.RAQO8QUmXsafzJV5drNpXRiEaN6knA06tWQLMcS1HqaH8130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP530812.RAQO8QUmXsafzJV5drNpXRiEaN6knA06tWQLMcS1HqaH8130_provenance.
- NP530812.RAQO8QUmXsafzJV5drNpXRiEaN6knA06tWQLMcS1HqaH8130_assertion description "[In the present investigation, we analyzed the value of commonly used clinical tests (electroencephalogram [EEG], detection of 14-3-3 protein in cerebrospinal fluid [CSF], and hyperintensity of the basal ganglia in magnetic resonance imaging) for the clinical diagnosis in each CJD phenotype.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP530812.RAQO8QUmXsafzJV5drNpXRiEaN6knA06tWQLMcS1HqaH8130_provenance.
- NP530812.RAQO8QUmXsafzJV5drNpXRiEaN6knA06tWQLMcS1HqaH8130_assertion evidence source_evidence_literature NP530812.RAQO8QUmXsafzJV5drNpXRiEaN6knA06tWQLMcS1HqaH8130_provenance.
- NP530812.RAQO8QUmXsafzJV5drNpXRiEaN6knA06tWQLMcS1HqaH8130_assertion SIO_000772 10976638 NP530812.RAQO8QUmXsafzJV5drNpXRiEaN6knA06tWQLMcS1HqaH8130_provenance.
- NP530812.RAQO8QUmXsafzJV5drNpXRiEaN6knA06tWQLMcS1HqaH8130_assertion wasDerivedFrom befree-20150227 NP530812.RAQO8QUmXsafzJV5drNpXRiEaN6knA06tWQLMcS1HqaH8130_provenance.
- NP530812.RAQO8QUmXsafzJV5drNpXRiEaN6knA06tWQLMcS1HqaH8130_assertion wasGeneratedBy ECO_0000203 NP530812.RAQO8QUmXsafzJV5drNpXRiEaN6knA06tWQLMcS1HqaH8130_provenance.
- befree-20150227 importedOn "2015-02-27" NP530812.RAQO8QUmXsafzJV5drNpXRiEaN6knA06tWQLMcS1HqaH8130_provenance.