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- source_evidence_literature type ECO_0000212 NP1246118.RA2VfA66CilPeidtmP9N435t33_6Yk9b_SPEVXFg0B3EI130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP1246118.RA2VfA66CilPeidtmP9N435t33_6Yk9b_SPEVXFg0B3EI130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP1246118.RA2VfA66CilPeidtmP9N435t33_6Yk9b_SPEVXFg0B3EI130_provenance.
- NP1246118.RA2VfA66CilPeidtmP9N435t33_6Yk9b_SPEVXFg0B3EI130_assertion description "[We performed polymerase chain reaction-denaturing high performance liquid chromatography (PCR-DHPLC) followed by direct sequencing to detect IDH mutations in 237 patients with myeloproliferative neoplasms (MPNs; n=108), myelodysplastic syndrome (MDS; n=22), paroxysmal nocturnal hemoglobinuria (PNH; n=41), and aplastic anemia (AA; n=66).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1246118.RA2VfA66CilPeidtmP9N435t33_6Yk9b_SPEVXFg0B3EI130_provenance.
- NP1246118.RA2VfA66CilPeidtmP9N435t33_6Yk9b_SPEVXFg0B3EI130_assertion evidence source_evidence_literature NP1246118.RA2VfA66CilPeidtmP9N435t33_6Yk9b_SPEVXFg0B3EI130_provenance.
- NP1246118.RA2VfA66CilPeidtmP9N435t33_6Yk9b_SPEVXFg0B3EI130_assertion SIO_000772 25486927 NP1246118.RA2VfA66CilPeidtmP9N435t33_6Yk9b_SPEVXFg0B3EI130_provenance.
- NP1246118.RA2VfA66CilPeidtmP9N435t33_6Yk9b_SPEVXFg0B3EI130_assertion wasDerivedFrom befree-2016 NP1246118.RA2VfA66CilPeidtmP9N435t33_6Yk9b_SPEVXFg0B3EI130_provenance.
- NP1246118.RA2VfA66CilPeidtmP9N435t33_6Yk9b_SPEVXFg0B3EI130_assertion wasGeneratedBy ECO_0000203 NP1246118.RA2VfA66CilPeidtmP9N435t33_6Yk9b_SPEVXFg0B3EI130_provenance.
- befree-2016 importedOn "2016-02-19" NP1246118.RA2VfA66CilPeidtmP9N435t33_6Yk9b_SPEVXFg0B3EI130_provenance.