Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP802184.RAnQ6nishVuIwkFiWvfrNuvMlhRxCQk2F4FtHrUAB-LVo130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP802184.RAnQ6nishVuIwkFiWvfrNuvMlhRxCQk2F4FtHrUAB-LVo130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP802184.RAnQ6nishVuIwkFiWvfrNuvMlhRxCQk2F4FtHrUAB-LVo130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP802184.RAnQ6nishVuIwkFiWvfrNuvMlhRxCQk2F4FtHrUAB-LVo130_provenance.
- NP802184.RAnQ6nishVuIwkFiWvfrNuvMlhRxCQk2F4FtHrUAB-LVo130_assertion description "[The methylation frequencies of the 10 genes examined in NSCLC were 26% for DAPK, 34% for FHIT, 26% for H-cadherin, 14% for MGMT, 8% for p14, 27% for p16, 38% for RAR-beta, 42% for RASSF1A, 25% for RUNX3, and 12% for TIMP-3.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP802184.RAnQ6nishVuIwkFiWvfrNuvMlhRxCQk2F4FtHrUAB-LVo130_provenance.
- NP802184.RAnQ6nishVuIwkFiWvfrNuvMlhRxCQk2F4FtHrUAB-LVo130_assertion evidence source_evidence_literature NP802184.RAnQ6nishVuIwkFiWvfrNuvMlhRxCQk2F4FtHrUAB-LVo130_provenance.
- NP802184.RAnQ6nishVuIwkFiWvfrNuvMlhRxCQk2F4FtHrUAB-LVo130_assertion SIO_000772 17606310 NP802184.RAnQ6nishVuIwkFiWvfrNuvMlhRxCQk2F4FtHrUAB-LVo130_provenance.
- NP802184.RAnQ6nishVuIwkFiWvfrNuvMlhRxCQk2F4FtHrUAB-LVo130_assertion wasDerivedFrom befree-20140225 NP802184.RAnQ6nishVuIwkFiWvfrNuvMlhRxCQk2F4FtHrUAB-LVo130_provenance.
- NP802184.RAnQ6nishVuIwkFiWvfrNuvMlhRxCQk2F4FtHrUAB-LVo130_assertion wasGeneratedBy ECO_0000203 NP802184.RAnQ6nishVuIwkFiWvfrNuvMlhRxCQk2F4FtHrUAB-LVo130_provenance.
- befree-20140225 importedOn "2014-02-25" NP802184.RAnQ6nishVuIwkFiWvfrNuvMlhRxCQk2F4FtHrUAB-LVo130_provenance.