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- source_evidence_literature type ECO_0000212 NP723915.RAVAkVrErjz9TqQT0KM_4f8fdfccrFZlNmQ0jH_ML9zVk130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP723915.RAVAkVrErjz9TqQT0KM_4f8fdfccrFZlNmQ0jH_ML9zVk130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP723915.RAVAkVrErjz9TqQT0KM_4f8fdfccrFZlNmQ0jH_ML9zVk130_provenance.
- NP723915.RAVAkVrErjz9TqQT0KM_4f8fdfccrFZlNmQ0jH_ML9zVk130_assertion description "[Mutations in the PRRT2 gene have been recently described as a cause of paroxysmal kinesigenic dyskinesia, infantile convulsions with choreoathetosis syndrome and, less often, infantile convulsions.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP723915.RAVAkVrErjz9TqQT0KM_4f8fdfccrFZlNmQ0jH_ML9zVk130_provenance.
- NP723915.RAVAkVrErjz9TqQT0KM_4f8fdfccrFZlNmQ0jH_ML9zVk130_assertion evidence source_evidence_literature NP723915.RAVAkVrErjz9TqQT0KM_4f8fdfccrFZlNmQ0jH_ML9zVk130_provenance.
- NP723915.RAVAkVrErjz9TqQT0KM_4f8fdfccrFZlNmQ0jH_ML9zVk130_assertion SIO_000772 22877996 NP723915.RAVAkVrErjz9TqQT0KM_4f8fdfccrFZlNmQ0jH_ML9zVk130_provenance.
- NP723915.RAVAkVrErjz9TqQT0KM_4f8fdfccrFZlNmQ0jH_ML9zVk130_assertion wasDerivedFrom befree-20140225 NP723915.RAVAkVrErjz9TqQT0KM_4f8fdfccrFZlNmQ0jH_ML9zVk130_provenance.
- NP723915.RAVAkVrErjz9TqQT0KM_4f8fdfccrFZlNmQ0jH_ML9zVk130_assertion wasGeneratedBy ECO_0000203 NP723915.RAVAkVrErjz9TqQT0KM_4f8fdfccrFZlNmQ0jH_ML9zVk130_provenance.
- befree-20140225 importedOn "2014-02-25" NP723915.RAVAkVrErjz9TqQT0KM_4f8fdfccrFZlNmQ0jH_ML9zVk130_provenance.