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- source_evidence_literature type ECO_0000212 NP657566.RAmHl2IOU69qk9JbZ4MGCK_fve-fWKtfRFwVg8pVgFxm0130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP657566.RAmHl2IOU69qk9JbZ4MGCK_fve-fWKtfRFwVg8pVgFxm0130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP657566.RAmHl2IOU69qk9JbZ4MGCK_fve-fWKtfRFwVg8pVgFxm0130_provenance.
- NP657566.RAmHl2IOU69qk9JbZ4MGCK_fve-fWKtfRFwVg8pVgFxm0130_assertion description "[In summary, we conclude that genetic variations in UBQLN2 and PFN1 in a predominantly Flanders-Belgian cohort of FTLD and ALS patients are extremely rare.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP657566.RAmHl2IOU69qk9JbZ4MGCK_fve-fWKtfRFwVg8pVgFxm0130_provenance.
- NP657566.RAmHl2IOU69qk9JbZ4MGCK_fve-fWKtfRFwVg8pVgFxm0130_assertion evidence source_evidence_literature NP657566.RAmHl2IOU69qk9JbZ4MGCK_fve-fWKtfRFwVg8pVgFxm0130_provenance.
- NP657566.RAmHl2IOU69qk9JbZ4MGCK_fve-fWKtfRFwVg8pVgFxm0130_assertion SIO_000772 23312802 NP657566.RAmHl2IOU69qk9JbZ4MGCK_fve-fWKtfRFwVg8pVgFxm0130_provenance.
- NP657566.RAmHl2IOU69qk9JbZ4MGCK_fve-fWKtfRFwVg8pVgFxm0130_assertion wasDerivedFrom befree-20140225 NP657566.RAmHl2IOU69qk9JbZ4MGCK_fve-fWKtfRFwVg8pVgFxm0130_provenance.
- NP657566.RAmHl2IOU69qk9JbZ4MGCK_fve-fWKtfRFwVg8pVgFxm0130_assertion wasGeneratedBy ECO_0000203 NP657566.RAmHl2IOU69qk9JbZ4MGCK_fve-fWKtfRFwVg8pVgFxm0130_provenance.
- befree-20140225 importedOn "2014-02-25" NP657566.RAmHl2IOU69qk9JbZ4MGCK_fve-fWKtfRFwVg8pVgFxm0130_provenance.