Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP434494.RA1o8nuxt5lTFN6jhk7EMa6Zc7Bw9WLebh54I_PZOXfHQ130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP434494.RA1o8nuxt5lTFN6jhk7EMa6Zc7Bw9WLebh54I_PZOXfHQ130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP434494.RA1o8nuxt5lTFN6jhk7EMa6Zc7Bw9WLebh54I_PZOXfHQ130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP434494.RA1o8nuxt5lTFN6jhk7EMa6Zc7Bw9WLebh54I_PZOXfHQ130_provenance.
- NP434494.RA1o8nuxt5lTFN6jhk7EMa6Zc7Bw9WLebh54I_PZOXfHQ130_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." NP434494.RA1o8nuxt5lTFN6jhk7EMa6Zc7Bw9WLebh54I_PZOXfHQ130_provenance.
- NP434494.RA1o8nuxt5lTFN6jhk7EMa6Zc7Bw9WLebh54I_PZOXfHQ130_assertion evidence source_evidence_literature NP434494.RA1o8nuxt5lTFN6jhk7EMa6Zc7Bw9WLebh54I_PZOXfHQ130_provenance.
- NP434494.RA1o8nuxt5lTFN6jhk7EMa6Zc7Bw9WLebh54I_PZOXfHQ130_assertion SIO_000772 23933820 NP434494.RA1o8nuxt5lTFN6jhk7EMa6Zc7Bw9WLebh54I_PZOXfHQ130_provenance.
- NP434494.RA1o8nuxt5lTFN6jhk7EMa6Zc7Bw9WLebh54I_PZOXfHQ130_assertion wasDerivedFrom befree-20150227 NP434494.RA1o8nuxt5lTFN6jhk7EMa6Zc7Bw9WLebh54I_PZOXfHQ130_provenance.
- NP434494.RA1o8nuxt5lTFN6jhk7EMa6Zc7Bw9WLebh54I_PZOXfHQ130_assertion wasGeneratedBy ECO_0000203 NP434494.RA1o8nuxt5lTFN6jhk7EMa6Zc7Bw9WLebh54I_PZOXfHQ130_provenance.
- befree-20150227 importedOn "2015-02-27" NP434494.RA1o8nuxt5lTFN6jhk7EMa6Zc7Bw9WLebh54I_PZOXfHQ130_provenance.