Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP338549.RADIftUO9579vulY_9At9F4mFiXgAaxlUVQ_Ln9nD67wo130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP338549.RADIftUO9579vulY_9At9F4mFiXgAaxlUVQ_Ln9nD67wo130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP338549.RADIftUO9579vulY_9At9F4mFiXgAaxlUVQ_Ln9nD67wo130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP338549.RADIftUO9579vulY_9At9F4mFiXgAaxlUVQ_Ln9nD67wo130_provenance.
- NP338549.RADIftUO9579vulY_9At9F4mFiXgAaxlUVQ_Ln9nD67wo130_assertion description "[These observations indicate that: 1) Ery-UROD activity may not always be useful to discriminate between F-PCT and HEP; 2) Ery-UROD activity does not always correlate with clinical symptoms; 3) in inherited UROD deficiency, the genetic defect may be heterogeneous.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP338549.RADIftUO9579vulY_9At9F4mFiXgAaxlUVQ_Ln9nD67wo130_provenance.
- NP338549.RADIftUO9579vulY_9At9F4mFiXgAaxlUVQ_Ln9nD67wo130_assertion evidence source_evidence_literature NP338549.RADIftUO9579vulY_9At9F4mFiXgAaxlUVQ_Ln9nD67wo130_provenance.
- NP338549.RADIftUO9579vulY_9At9F4mFiXgAaxlUVQ_Ln9nD67wo130_assertion SIO_000772 9427577 NP338549.RADIftUO9579vulY_9At9F4mFiXgAaxlUVQ_Ln9nD67wo130_provenance.
- NP338549.RADIftUO9579vulY_9At9F4mFiXgAaxlUVQ_Ln9nD67wo130_assertion wasDerivedFrom befree-20140225 NP338549.RADIftUO9579vulY_9At9F4mFiXgAaxlUVQ_Ln9nD67wo130_provenance.
- NP338549.RADIftUO9579vulY_9At9F4mFiXgAaxlUVQ_Ln9nD67wo130_assertion wasGeneratedBy ECO_0000203 NP338549.RADIftUO9579vulY_9At9F4mFiXgAaxlUVQ_Ln9nD67wo130_provenance.
- befree-20140225 importedOn "2014-02-25" NP338549.RADIftUO9579vulY_9At9F4mFiXgAaxlUVQ_Ln9nD67wo130_provenance.