Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP478810.RAa5W7_RGxbf3tNub_bTBMIztnrs_oCbFmEQ28hTplMCo130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP478810.RAa5W7_RGxbf3tNub_bTBMIztnrs_oCbFmEQ28hTplMCo130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP478810.RAa5W7_RGxbf3tNub_bTBMIztnrs_oCbFmEQ28hTplMCo130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP478810.RAa5W7_RGxbf3tNub_bTBMIztnrs_oCbFmEQ28hTplMCo130_provenance.
- NP478810.RAa5W7_RGxbf3tNub_bTBMIztnrs_oCbFmEQ28hTplMCo130_assertion description "[HCV genotype 1b was detected in 100 of the 143 ASC (69.9%), 551 of the 726 NC-CH patients (75.9%), 86 of the 103 patients with LC (83.5%), and 153 of the 179 HCC (85.5%) patients.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP478810.RAa5W7_RGxbf3tNub_bTBMIztnrs_oCbFmEQ28hTplMCo130_provenance.
- NP478810.RAa5W7_RGxbf3tNub_bTBMIztnrs_oCbFmEQ28hTplMCo130_assertion evidence source_evidence_literature NP478810.RAa5W7_RGxbf3tNub_bTBMIztnrs_oCbFmEQ28hTplMCo130_provenance.
- NP478810.RAa5W7_RGxbf3tNub_bTBMIztnrs_oCbFmEQ28hTplMCo130_assertion SIO_000772 9816816 NP478810.RAa5W7_RGxbf3tNub_bTBMIztnrs_oCbFmEQ28hTplMCo130_provenance.
- NP478810.RAa5W7_RGxbf3tNub_bTBMIztnrs_oCbFmEQ28hTplMCo130_assertion wasDerivedFrom befree-20140225 NP478810.RAa5W7_RGxbf3tNub_bTBMIztnrs_oCbFmEQ28hTplMCo130_provenance.
- NP478810.RAa5W7_RGxbf3tNub_bTBMIztnrs_oCbFmEQ28hTplMCo130_assertion wasGeneratedBy ECO_0000203 NP478810.RAa5W7_RGxbf3tNub_bTBMIztnrs_oCbFmEQ28hTplMCo130_provenance.
- befree-20140225 importedOn "2014-02-25" NP478810.RAa5W7_RGxbf3tNub_bTBMIztnrs_oCbFmEQ28hTplMCo130_provenance.