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- source_evidence_literature type ECO_0000212 NP756093.RAN18Z44e1Pq4ghxDRkm_gKA52On_aV5zDydo0Bi3avHo130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP756093.RAN18Z44e1Pq4ghxDRkm_gKA52On_aV5zDydo0Bi3avHo130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP756093.RAN18Z44e1Pq4ghxDRkm_gKA52On_aV5zDydo0Bi3avHo130_provenance.
- NP756093.RAN18Z44e1Pq4ghxDRkm_gKA52On_aV5zDydo0Bi3avHo130_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." NP756093.RAN18Z44e1Pq4ghxDRkm_gKA52On_aV5zDydo0Bi3avHo130_provenance.
- NP756093.RAN18Z44e1Pq4ghxDRkm_gKA52On_aV5zDydo0Bi3avHo130_assertion evidence source_evidence_literature NP756093.RAN18Z44e1Pq4ghxDRkm_gKA52On_aV5zDydo0Bi3avHo130_provenance.
- NP756093.RAN18Z44e1Pq4ghxDRkm_gKA52On_aV5zDydo0Bi3avHo130_assertion SIO_000772 22913971 NP756093.RAN18Z44e1Pq4ghxDRkm_gKA52On_aV5zDydo0Bi3avHo130_provenance.
- NP756093.RAN18Z44e1Pq4ghxDRkm_gKA52On_aV5zDydo0Bi3avHo130_assertion wasDerivedFrom befree-20140225 NP756093.RAN18Z44e1Pq4ghxDRkm_gKA52On_aV5zDydo0Bi3avHo130_provenance.
- NP756093.RAN18Z44e1Pq4ghxDRkm_gKA52On_aV5zDydo0Bi3avHo130_assertion wasGeneratedBy ECO_0000203 NP756093.RAN18Z44e1Pq4ghxDRkm_gKA52On_aV5zDydo0Bi3avHo130_provenance.
- befree-20140225 importedOn "2014-02-25" NP756093.RAN18Z44e1Pq4ghxDRkm_gKA52On_aV5zDydo0Bi3avHo130_provenance.