Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP258794.RAAbBNev4sSAlGh5HVvF4bCJERxh0wNWgmdTATQXODS6Y130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP258794.RAAbBNev4sSAlGh5HVvF4bCJERxh0wNWgmdTATQXODS6Y130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP258794.RAAbBNev4sSAlGh5HVvF4bCJERxh0wNWgmdTATQXODS6Y130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP258794.RAAbBNev4sSAlGh5HVvF4bCJERxh0wNWgmdTATQXODS6Y130_provenance.
- befree-2016 importedOn "2016-02-19" NP258794.RAAbBNev4sSAlGh5HVvF4bCJERxh0wNWgmdTATQXODS6Y130_provenance.
- NP258794.RAAbBNev4sSAlGh5HVvF4bCJERxh0wNWgmdTATQXODS6Y130_assertion wasGeneratedBy ECO_0000203 NP258794.RAAbBNev4sSAlGh5HVvF4bCJERxh0wNWgmdTATQXODS6Y130_provenance.
- NP258794.RAAbBNev4sSAlGh5HVvF4bCJERxh0wNWgmdTATQXODS6Y130_assertion wasDerivedFrom befree-2016 NP258794.RAAbBNev4sSAlGh5HVvF4bCJERxh0wNWgmdTATQXODS6Y130_provenance.
- NP258794.RAAbBNev4sSAlGh5HVvF4bCJERxh0wNWgmdTATQXODS6Y130_assertion SIO_000772 10424811 NP258794.RAAbBNev4sSAlGh5HVvF4bCJERxh0wNWgmdTATQXODS6Y130_provenance.
- NP258794.RAAbBNev4sSAlGh5HVvF4bCJERxh0wNWgmdTATQXODS6Y130_assertion evidence source_evidence_literature NP258794.RAAbBNev4sSAlGh5HVvF4bCJERxh0wNWgmdTATQXODS6Y130_provenance.
- NP258794.RAAbBNev4sSAlGh5HVvF4bCJERxh0wNWgmdTATQXODS6Y130_assertion description "[A total of 70 patients with classical BWS were investigated; 54 were sporadic with no evidence of UPD and 16 were familial from seven kindreds.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP258794.RAAbBNev4sSAlGh5HVvF4bCJERxh0wNWgmdTATQXODS6Y130_provenance.