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- source_evidence_literature type ECO_0000212 NP676861.RAQOyQ1PTDtpGEA5ahf3HggH2-Nrnb8b4sS_B3fYPsZuE130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP676861.RAQOyQ1PTDtpGEA5ahf3HggH2-Nrnb8b4sS_B3fYPsZuE130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP676861.RAQOyQ1PTDtpGEA5ahf3HggH2-Nrnb8b4sS_B3fYPsZuE130_provenance.
- befree-20150227 importedOn "2015-02-27" NP676861.RAQOyQ1PTDtpGEA5ahf3HggH2-Nrnb8b4sS_B3fYPsZuE130_provenance.
- NP676861.RAQOyQ1PTDtpGEA5ahf3HggH2-Nrnb8b4sS_B3fYPsZuE130_assertion wasGeneratedBy ECO_0000203 NP676861.RAQOyQ1PTDtpGEA5ahf3HggH2-Nrnb8b4sS_B3fYPsZuE130_provenance.
- NP676861.RAQOyQ1PTDtpGEA5ahf3HggH2-Nrnb8b4sS_B3fYPsZuE130_assertion wasDerivedFrom befree-20150227 NP676861.RAQOyQ1PTDtpGEA5ahf3HggH2-Nrnb8b4sS_B3fYPsZuE130_provenance.
- NP676861.RAQOyQ1PTDtpGEA5ahf3HggH2-Nrnb8b4sS_B3fYPsZuE130_assertion SIO_000772 9307247 NP676861.RAQOyQ1PTDtpGEA5ahf3HggH2-Nrnb8b4sS_B3fYPsZuE130_provenance.
- NP676861.RAQOyQ1PTDtpGEA5ahf3HggH2-Nrnb8b4sS_B3fYPsZuE130_assertion evidence source_evidence_literature NP676861.RAQOyQ1PTDtpGEA5ahf3HggH2-Nrnb8b4sS_B3fYPsZuE130_provenance.
- NP676861.RAQOyQ1PTDtpGEA5ahf3HggH2-Nrnb8b4sS_B3fYPsZuE130_assertion description "[These include the L-type voltage-gated calcium channel of skeletal muscle (hypokalemic periodic paralysis), the neuronal P/Q-type voltage-gated calcium channel (familial hemiplegic migraine, episodic ataxia type 2, spinocerebellar ataxia 6, and Lambert-Eaton myasthenic syndrome), and the skeletal muscle ryanodine receptor (malignant hyperthermia and central core disease).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP676861.RAQOyQ1PTDtpGEA5ahf3HggH2-Nrnb8b4sS_B3fYPsZuE130_provenance.