Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP743289.RA8iziDAbaYiAGi6nLI1StfToyOH8N1fpkndrVGp4oJwM130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP743289.RA8iziDAbaYiAGi6nLI1StfToyOH8N1fpkndrVGp4oJwM130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP743289.RA8iziDAbaYiAGi6nLI1StfToyOH8N1fpkndrVGp4oJwM130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP743289.RA8iziDAbaYiAGi6nLI1StfToyOH8N1fpkndrVGp4oJwM130_provenance.
- NP743289.RA8iziDAbaYiAGi6nLI1StfToyOH8N1fpkndrVGp4oJwM130_assertion description "[The correlations of preS deletion with disease progression were distinct: preS deletion mutations were more commonly found in the hepatocellular carcinoma (HCC) group than in the chronic hepatitis B (CHB) or asymptomatic carrier (ASC) groups, with the frequencies of 38.46% (10/26) in the HCC, 7.14% (2/28) in the CHB, and 4.00% (1/25) in the ASC (P = 0.001) groups.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP743289.RA8iziDAbaYiAGi6nLI1StfToyOH8N1fpkndrVGp4oJwM130_provenance.
- NP743289.RA8iziDAbaYiAGi6nLI1StfToyOH8N1fpkndrVGp4oJwM130_assertion evidence source_evidence_literature NP743289.RA8iziDAbaYiAGi6nLI1StfToyOH8N1fpkndrVGp4oJwM130_provenance.
- NP743289.RA8iziDAbaYiAGi6nLI1StfToyOH8N1fpkndrVGp4oJwM130_assertion SIO_000772 17876546 NP743289.RA8iziDAbaYiAGi6nLI1StfToyOH8N1fpkndrVGp4oJwM130_provenance.
- NP743289.RA8iziDAbaYiAGi6nLI1StfToyOH8N1fpkndrVGp4oJwM130_assertion wasDerivedFrom befree-20140225 NP743289.RA8iziDAbaYiAGi6nLI1StfToyOH8N1fpkndrVGp4oJwM130_provenance.
- NP743289.RA8iziDAbaYiAGi6nLI1StfToyOH8N1fpkndrVGp4oJwM130_assertion wasGeneratedBy ECO_0000203 NP743289.RA8iziDAbaYiAGi6nLI1StfToyOH8N1fpkndrVGp4oJwM130_provenance.
- befree-20140225 importedOn "2014-02-25" NP743289.RA8iziDAbaYiAGi6nLI1StfToyOH8N1fpkndrVGp4oJwM130_provenance.