Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP173279.RA3g15fhAaXslVBwe38mQgQDOtW-gCQT3Cs-OyZIp4meA130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP173279.RA3g15fhAaXslVBwe38mQgQDOtW-gCQT3Cs-OyZIp4meA130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP173279.RA3g15fhAaXslVBwe38mQgQDOtW-gCQT3Cs-OyZIp4meA130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP173279.RA3g15fhAaXslVBwe38mQgQDOtW-gCQT3Cs-OyZIp4meA130_provenance.
- NP173279.RA3g15fhAaXslVBwe38mQgQDOtW-gCQT3Cs-OyZIp4meA130_assertion description "[Next-generation molecular biology technologies have recently identified recurrent CIC and FUBP1 point mutations in 1p/19q codeleted and IDH-mutated oligodendrogliomas.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP173279.RA3g15fhAaXslVBwe38mQgQDOtW-gCQT3Cs-OyZIp4meA130_provenance.
- NP173279.RA3g15fhAaXslVBwe38mQgQDOtW-gCQT3Cs-OyZIp4meA130_assertion evidence source_evidence_literature NP173279.RA3g15fhAaXslVBwe38mQgQDOtW-gCQT3Cs-OyZIp4meA130_provenance.
- NP173279.RA3g15fhAaXslVBwe38mQgQDOtW-gCQT3Cs-OyZIp4meA130_assertion SIO_000772 22913971 NP173279.RA3g15fhAaXslVBwe38mQgQDOtW-gCQT3Cs-OyZIp4meA130_provenance.
- NP173279.RA3g15fhAaXslVBwe38mQgQDOtW-gCQT3Cs-OyZIp4meA130_assertion wasDerivedFrom befree-20140225 NP173279.RA3g15fhAaXslVBwe38mQgQDOtW-gCQT3Cs-OyZIp4meA130_provenance.
- NP173279.RA3g15fhAaXslVBwe38mQgQDOtW-gCQT3Cs-OyZIp4meA130_assertion wasGeneratedBy ECO_0000203 NP173279.RA3g15fhAaXslVBwe38mQgQDOtW-gCQT3Cs-OyZIp4meA130_provenance.
- befree-20140225 importedOn "2014-02-25" NP173279.RA3g15fhAaXslVBwe38mQgQDOtW-gCQT3Cs-OyZIp4meA130_provenance.