Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP717276.RAT8pAiWIofommFho9Q55dWrAWRXFRhakvPCkI0rL01cU130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP717276.RAT8pAiWIofommFho9Q55dWrAWRXFRhakvPCkI0rL01cU130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP717276.RAT8pAiWIofommFho9Q55dWrAWRXFRhakvPCkI0rL01cU130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP717276.RAT8pAiWIofommFho9Q55dWrAWRXFRhakvPCkI0rL01cU130_provenance.
- NP717276.RAT8pAiWIofommFho9Q55dWrAWRXFRhakvPCkI0rL01cU130_assertion description "[Mutations in SCN2A, the gene encoding the brain voltage-gated sodium channel alpha-subunit Na(V)1.2, are associated with inherited epilepsies including benign familial neonatal-infantile seizures (BFNIS).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP717276.RAT8pAiWIofommFho9Q55dWrAWRXFRhakvPCkI0rL01cU130_provenance.
- NP717276.RAT8pAiWIofommFho9Q55dWrAWRXFRhakvPCkI0rL01cU130_assertion evidence source_evidence_literature NP717276.RAT8pAiWIofommFho9Q55dWrAWRXFRhakvPCkI0rL01cU130_provenance.
- NP717276.RAT8pAiWIofommFho9Q55dWrAWRXFRhakvPCkI0rL01cU130_assertion SIO_000772 18479388 NP717276.RAT8pAiWIofommFho9Q55dWrAWRXFRhakvPCkI0rL01cU130_provenance.
- NP717276.RAT8pAiWIofommFho9Q55dWrAWRXFRhakvPCkI0rL01cU130_assertion wasDerivedFrom befree-20140225 NP717276.RAT8pAiWIofommFho9Q55dWrAWRXFRhakvPCkI0rL01cU130_provenance.
- NP717276.RAT8pAiWIofommFho9Q55dWrAWRXFRhakvPCkI0rL01cU130_assertion wasGeneratedBy ECO_0000203 NP717276.RAT8pAiWIofommFho9Q55dWrAWRXFRhakvPCkI0rL01cU130_provenance.
- befree-20140225 importedOn "2014-02-25" NP717276.RAT8pAiWIofommFho9Q55dWrAWRXFRhakvPCkI0rL01cU130_provenance.