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- source_evidence_literature type ECO_0000212 NP653091.RA0FX7F4gGOXPPQG06F7nRn_N-cT1LAEwPMf7f6jyeU7A130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP653091.RA0FX7F4gGOXPPQG06F7nRn_N-cT1LAEwPMf7f6jyeU7A130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP653091.RA0FX7F4gGOXPPQG06F7nRn_N-cT1LAEwPMf7f6jyeU7A130_provenance.
- befree-20150227 importedOn "2015-02-27" NP653091.RA0FX7F4gGOXPPQG06F7nRn_N-cT1LAEwPMf7f6jyeU7A130_provenance.
- NP653091.RA0FX7F4gGOXPPQG06F7nRn_N-cT1LAEwPMf7f6jyeU7A130_assertion wasGeneratedBy ECO_0000203 NP653091.RA0FX7F4gGOXPPQG06F7nRn_N-cT1LAEwPMf7f6jyeU7A130_provenance.
- NP653091.RA0FX7F4gGOXPPQG06F7nRn_N-cT1LAEwPMf7f6jyeU7A130_assertion wasDerivedFrom befree-20150227 NP653091.RA0FX7F4gGOXPPQG06F7nRn_N-cT1LAEwPMf7f6jyeU7A130_provenance.
- NP653091.RA0FX7F4gGOXPPQG06F7nRn_N-cT1LAEwPMf7f6jyeU7A130_assertion SIO_000772 24405857 NP653091.RA0FX7F4gGOXPPQG06F7nRn_N-cT1LAEwPMf7f6jyeU7A130_provenance.
- NP653091.RA0FX7F4gGOXPPQG06F7nRn_N-cT1LAEwPMf7f6jyeU7A130_assertion evidence source_evidence_literature NP653091.RA0FX7F4gGOXPPQG06F7nRn_N-cT1LAEwPMf7f6jyeU7A130_provenance.
- NP653091.RA0FX7F4gGOXPPQG06F7nRn_N-cT1LAEwPMf7f6jyeU7A130_assertion description "[Several diagnostic and prognostic molecular markers such as BRAF and RAS point mutations; RET/PTC and PAX8/PPARγ gene rearrangements; MAPK, PI3K, p53, Wnt-beta catenin, HIF1α and NF-kappaB signaling pathways; microRNA profiles and aberrant methylation have been demonstrated in more than 70% of DTC.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP653091.RA0FX7F4gGOXPPQG06F7nRn_N-cT1LAEwPMf7f6jyeU7A130_provenance.