Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP33302.RAr7G_gBqs59p_wMUnnepePxvjLACujnfTFr8yD0lxvY8130_provenance>. }
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- source_evidence_curated type ECO_0000205 NP33302.RAr7G_gBqs59p_wMUnnepePxvjLACujnfTFr8yD0lxvY8130_provenance.
- source_evidence_curated label "DisGeNET evidence - CURATED" NP33302.RAr7G_gBqs59p_wMUnnepePxvjLACujnfTFr8yD0lxvY8130_provenance.
- source_evidence_curated comment "Gene-disease associations manually curated." NP33302.RAr7G_gBqs59p_wMUnnepePxvjLACujnfTFr8yD0lxvY8130_provenance.
- NP33302.RAr7G_gBqs59p_wMUnnepePxvjLACujnfTFr8yD0lxvY8130_assertion description "[GRIN2A mutations in acquired epileptic aphasia and related childhood focal epilepsies and encephalopathies with speech and language dysfunction.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP33302.RAr7G_gBqs59p_wMUnnepePxvjLACujnfTFr8yD0lxvY8130_provenance.
- NP33302.RAr7G_gBqs59p_wMUnnepePxvjLACujnfTFr8yD0lxvY8130_assertion evidence source_evidence_curated NP33302.RAr7G_gBqs59p_wMUnnepePxvjLACujnfTFr8yD0lxvY8130_provenance.
- NP33302.RAr7G_gBqs59p_wMUnnepePxvjLACujnfTFr8yD0lxvY8130_assertion SIO_000772 23933820 NP33302.RAr7G_gBqs59p_wMUnnepePxvjLACujnfTFr8yD0lxvY8130_provenance.
- NP33302.RAr7G_gBqs59p_wMUnnepePxvjLACujnfTFr8yD0lxvY8130_assertion wasDerivedFrom ctd_human-2016 NP33302.RAr7G_gBqs59p_wMUnnepePxvjLACujnfTFr8yD0lxvY8130_provenance.
- NP33302.RAr7G_gBqs59p_wMUnnepePxvjLACujnfTFr8yD0lxvY8130_assertion wasGeneratedBy ECO_0000218 NP33302.RAr7G_gBqs59p_wMUnnepePxvjLACujnfTFr8yD0lxvY8130_provenance.
- ctd_human-2016 importedOn "2016-01-25" NP33302.RAr7G_gBqs59p_wMUnnepePxvjLACujnfTFr8yD0lxvY8130_provenance.