Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP778515.RAedwLR_MDJjndJnIhvc6X1--kUV0w_tq_MnbLiPc1bOU130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP778515.RAedwLR_MDJjndJnIhvc6X1--kUV0w_tq_MnbLiPc1bOU130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP778515.RAedwLR_MDJjndJnIhvc6X1--kUV0w_tq_MnbLiPc1bOU130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP778515.RAedwLR_MDJjndJnIhvc6X1--kUV0w_tq_MnbLiPc1bOU130_provenance.
- NP778515.RAedwLR_MDJjndJnIhvc6X1--kUV0w_tq_MnbLiPc1bOU130_assertion description "[RAR?, TMEFF2 and CYGB displayed no apparent methylation, while a combinatory epigenotype based on p16, hTERT, RASSF1 and WT1 was associated with a significantly higher chance of detecting malignancy in any positive sample (odds ratio: 24, 95% CI: 4.7-125, P<0.001).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP778515.RAedwLR_MDJjndJnIhvc6X1--kUV0w_tq_MnbLiPc1bOU130_provenance.
- NP778515.RAedwLR_MDJjndJnIhvc6X1--kUV0w_tq_MnbLiPc1bOU130_assertion evidence source_evidence_literature NP778515.RAedwLR_MDJjndJnIhvc6X1--kUV0w_tq_MnbLiPc1bOU130_provenance.
- NP778515.RAedwLR_MDJjndJnIhvc6X1--kUV0w_tq_MnbLiPc1bOU130_assertion SIO_000772 21063414 NP778515.RAedwLR_MDJjndJnIhvc6X1--kUV0w_tq_MnbLiPc1bOU130_provenance.
- NP778515.RAedwLR_MDJjndJnIhvc6X1--kUV0w_tq_MnbLiPc1bOU130_assertion wasDerivedFrom befree-20150227 NP778515.RAedwLR_MDJjndJnIhvc6X1--kUV0w_tq_MnbLiPc1bOU130_provenance.
- NP778515.RAedwLR_MDJjndJnIhvc6X1--kUV0w_tq_MnbLiPc1bOU130_assertion wasGeneratedBy ECO_0000203 NP778515.RAedwLR_MDJjndJnIhvc6X1--kUV0w_tq_MnbLiPc1bOU130_provenance.
- befree-20150227 importedOn "2015-02-27" NP778515.RAedwLR_MDJjndJnIhvc6X1--kUV0w_tq_MnbLiPc1bOU130_provenance.