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- source_evidence_literature type ECO_0000212 NP1267598.RABmaQ_Y3_oPrNtJAc0nwkM-_JVYGlvD8i9iFYE61yUKo130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP1267598.RABmaQ_Y3_oPrNtJAc0nwkM-_JVYGlvD8i9iFYE61yUKo130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP1267598.RABmaQ_Y3_oPrNtJAc0nwkM-_JVYGlvD8i9iFYE61yUKo130_provenance.
- NP1267598.RABmaQ_Y3_oPrNtJAc0nwkM-_JVYGlvD8i9iFYE61yUKo130_assertion description "[By contrast, mutations affecting spliceosome genes SF3B1 and SRSF2, closely associated with the myelodysplastic syndromes, were identified only in those aged >70 years, with several individuals harboring more than one such mutation.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1267598.RABmaQ_Y3_oPrNtJAc0nwkM-_JVYGlvD8i9iFYE61yUKo130_provenance.
- NP1267598.RABmaQ_Y3_oPrNtJAc0nwkM-_JVYGlvD8i9iFYE61yUKo130_assertion evidence source_evidence_literature NP1267598.RABmaQ_Y3_oPrNtJAc0nwkM-_JVYGlvD8i9iFYE61yUKo130_provenance.
- NP1267598.RABmaQ_Y3_oPrNtJAc0nwkM-_JVYGlvD8i9iFYE61yUKo130_assertion SIO_000772 25732814 NP1267598.RABmaQ_Y3_oPrNtJAc0nwkM-_JVYGlvD8i9iFYE61yUKo130_provenance.
- NP1267598.RABmaQ_Y3_oPrNtJAc0nwkM-_JVYGlvD8i9iFYE61yUKo130_assertion wasDerivedFrom befree-2016 NP1267598.RABmaQ_Y3_oPrNtJAc0nwkM-_JVYGlvD8i9iFYE61yUKo130_provenance.
- NP1267598.RABmaQ_Y3_oPrNtJAc0nwkM-_JVYGlvD8i9iFYE61yUKo130_assertion wasGeneratedBy ECO_0000203 NP1267598.RABmaQ_Y3_oPrNtJAc0nwkM-_JVYGlvD8i9iFYE61yUKo130_provenance.
- befree-2016 importedOn "2016-02-19" NP1267598.RABmaQ_Y3_oPrNtJAc0nwkM-_JVYGlvD8i9iFYE61yUKo130_provenance.