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- source_evidence_literature type ECO_0000212 NP82289.RAKmpVuL5ZWF5NjpdidQJHkdZT07hLLiNVh-na-uR2fLU130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP82289.RAKmpVuL5ZWF5NjpdidQJHkdZT07hLLiNVh-na-uR2fLU130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP82289.RAKmpVuL5ZWF5NjpdidQJHkdZT07hLLiNVh-na-uR2fLU130_provenance.
- NP82289.RAKmpVuL5ZWF5NjpdidQJHkdZT07hLLiNVh-na-uR2fLU130_assertion description "[Mutations in the DYT1 gene can cause focal dystonia, and an association with a polymorphism in the D5 receptor gene (DRD5) has been reported but not confirmed.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP82289.RAKmpVuL5ZWF5NjpdidQJHkdZT07hLLiNVh-na-uR2fLU130_provenance.
- NP82289.RAKmpVuL5ZWF5NjpdidQJHkdZT07hLLiNVh-na-uR2fLU130_assertion evidence source_evidence_literature NP82289.RAKmpVuL5ZWF5NjpdidQJHkdZT07hLLiNVh-na-uR2fLU130_provenance.
- NP82289.RAKmpVuL5ZWF5NjpdidQJHkdZT07hLLiNVh-na-uR2fLU130_assertion SIO_000772 14581671 NP82289.RAKmpVuL5ZWF5NjpdidQJHkdZT07hLLiNVh-na-uR2fLU130_provenance.
- NP82289.RAKmpVuL5ZWF5NjpdidQJHkdZT07hLLiNVh-na-uR2fLU130_assertion wasDerivedFrom gad-20150221 NP82289.RAKmpVuL5ZWF5NjpdidQJHkdZT07hLLiNVh-na-uR2fLU130_provenance.
- NP82289.RAKmpVuL5ZWF5NjpdidQJHkdZT07hLLiNVh-na-uR2fLU130_assertion wasGeneratedBy ECO_0000203 NP82289.RAKmpVuL5ZWF5NjpdidQJHkdZT07hLLiNVh-na-uR2fLU130_provenance.
- gad-20150221 importedOn "2015-02-21" NP82289.RAKmpVuL5ZWF5NjpdidQJHkdZT07hLLiNVh-na-uR2fLU130_provenance.