Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP490817.RAphnoFYFOPPd5SnbaQDeHyTcHTF2qm1oF0HRw89ZocKk130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP490817.RAphnoFYFOPPd5SnbaQDeHyTcHTF2qm1oF0HRw89ZocKk130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP490817.RAphnoFYFOPPd5SnbaQDeHyTcHTF2qm1oF0HRw89ZocKk130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP490817.RAphnoFYFOPPd5SnbaQDeHyTcHTF2qm1oF0HRw89ZocKk130_provenance.
- NP490817.RAphnoFYFOPPd5SnbaQDeHyTcHTF2qm1oF0HRw89ZocKk130_assertion description "[The smallest commonly deleted region at 8p21.3-p22 in HCC and CRC was between the loci defined by C18-245 and C18-2644; in NSCLC, a region between C18-1051 and C18-2644 was commonly deleted.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP490817.RAphnoFYFOPPd5SnbaQDeHyTcHTF2qm1oF0HRw89ZocKk130_provenance.
- NP490817.RAphnoFYFOPPd5SnbaQDeHyTcHTF2qm1oF0HRw89ZocKk130_assertion evidence source_evidence_literature NP490817.RAphnoFYFOPPd5SnbaQDeHyTcHTF2qm1oF0HRw89ZocKk130_provenance.
- NP490817.RAphnoFYFOPPd5SnbaQDeHyTcHTF2qm1oF0HRw89ZocKk130_assertion SIO_000772 7519877 NP490817.RAphnoFYFOPPd5SnbaQDeHyTcHTF2qm1oF0HRw89ZocKk130_provenance.
- NP490817.RAphnoFYFOPPd5SnbaQDeHyTcHTF2qm1oF0HRw89ZocKk130_assertion wasDerivedFrom befree-20140225 NP490817.RAphnoFYFOPPd5SnbaQDeHyTcHTF2qm1oF0HRw89ZocKk130_provenance.
- NP490817.RAphnoFYFOPPd5SnbaQDeHyTcHTF2qm1oF0HRw89ZocKk130_assertion wasGeneratedBy ECO_0000203 NP490817.RAphnoFYFOPPd5SnbaQDeHyTcHTF2qm1oF0HRw89ZocKk130_provenance.
- befree-20140225 importedOn "2014-02-25" NP490817.RAphnoFYFOPPd5SnbaQDeHyTcHTF2qm1oF0HRw89ZocKk130_provenance.