Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP679845.RARYl0sF-G9NjIesDLQCal_V0KQsTGOOuxP6T_cqGTbEg130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP679845.RARYl0sF-G9NjIesDLQCal_V0KQsTGOOuxP6T_cqGTbEg130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP679845.RARYl0sF-G9NjIesDLQCal_V0KQsTGOOuxP6T_cqGTbEg130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP679845.RARYl0sF-G9NjIesDLQCal_V0KQsTGOOuxP6T_cqGTbEg130_provenance.
- NP679845.RARYl0sF-G9NjIesDLQCal_V0KQsTGOOuxP6T_cqGTbEg130_assertion description "[Quantitative MSP of the margins of 24 hypermethylation informative tumours revealed that 11 patients had molecularly positive margins, of which, five developed disease-specific events (DSEs, three local recurrences and two metastases), compared to none in patients with molecularly negative margins, after a median follow-up of 48 months.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP679845.RARYl0sF-G9NjIesDLQCal_V0KQsTGOOuxP6T_cqGTbEg130_provenance.
- NP679845.RARYl0sF-G9NjIesDLQCal_V0KQsTGOOuxP6T_cqGTbEg130_assertion evidence source_evidence_literature NP679845.RARYl0sF-G9NjIesDLQCal_V0KQsTGOOuxP6T_cqGTbEg130_provenance.
- NP679845.RARYl0sF-G9NjIesDLQCal_V0KQsTGOOuxP6T_cqGTbEg130_assertion SIO_000772 18594522 NP679845.RARYl0sF-G9NjIesDLQCal_V0KQsTGOOuxP6T_cqGTbEg130_provenance.
- NP679845.RARYl0sF-G9NjIesDLQCal_V0KQsTGOOuxP6T_cqGTbEg130_assertion wasDerivedFrom befree-2016 NP679845.RARYl0sF-G9NjIesDLQCal_V0KQsTGOOuxP6T_cqGTbEg130_provenance.
- NP679845.RARYl0sF-G9NjIesDLQCal_V0KQsTGOOuxP6T_cqGTbEg130_assertion wasGeneratedBy ECO_0000203 NP679845.RARYl0sF-G9NjIesDLQCal_V0KQsTGOOuxP6T_cqGTbEg130_provenance.
- befree-2016 importedOn "2016-02-19" NP679845.RARYl0sF-G9NjIesDLQCal_V0KQsTGOOuxP6T_cqGTbEg130_provenance.