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- source_evidence_literature type ECO_0000212 NP1217000.RAr8GfCEiamLYmh1fvYDHa-t7khCYrd6QtZuwdQiWh48k130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP1217000.RAr8GfCEiamLYmh1fvYDHa-t7khCYrd6QtZuwdQiWh48k130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP1217000.RAr8GfCEiamLYmh1fvYDHa-t7khCYrd6QtZuwdQiWh48k130_provenance.
- NP1217000.RAr8GfCEiamLYmh1fvYDHa-t7khCYrd6QtZuwdQiWh48k130_assertion description "[Some patients with primary hereditary erythrocytosis exhibit a mutation in the erythropoietin receptor (EPOR) which is associated with low serum erythropoietin (EPO) levels.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1217000.RAr8GfCEiamLYmh1fvYDHa-t7khCYrd6QtZuwdQiWh48k130_provenance.
- NP1217000.RAr8GfCEiamLYmh1fvYDHa-t7khCYrd6QtZuwdQiWh48k130_assertion evidence source_evidence_literature NP1217000.RAr8GfCEiamLYmh1fvYDHa-t7khCYrd6QtZuwdQiWh48k130_provenance.
- NP1217000.RAr8GfCEiamLYmh1fvYDHa-t7khCYrd6QtZuwdQiWh48k130_assertion SIO_000772 25189721 NP1217000.RAr8GfCEiamLYmh1fvYDHa-t7khCYrd6QtZuwdQiWh48k130_provenance.
- NP1217000.RAr8GfCEiamLYmh1fvYDHa-t7khCYrd6QtZuwdQiWh48k130_assertion wasDerivedFrom befree-2016 NP1217000.RAr8GfCEiamLYmh1fvYDHa-t7khCYrd6QtZuwdQiWh48k130_provenance.
- NP1217000.RAr8GfCEiamLYmh1fvYDHa-t7khCYrd6QtZuwdQiWh48k130_assertion wasGeneratedBy ECO_0000203 NP1217000.RAr8GfCEiamLYmh1fvYDHa-t7khCYrd6QtZuwdQiWh48k130_provenance.
- befree-2016 importedOn "2016-02-19" NP1217000.RAr8GfCEiamLYmh1fvYDHa-t7khCYrd6QtZuwdQiWh48k130_provenance.