Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP683854.RAf0ayETnpNDI8A7qUb08288-m6Yx18wLAlcpqkek-Auc130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP683854.RAf0ayETnpNDI8A7qUb08288-m6Yx18wLAlcpqkek-Auc130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP683854.RAf0ayETnpNDI8A7qUb08288-m6Yx18wLAlcpqkek-Auc130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP683854.RAf0ayETnpNDI8A7qUb08288-m6Yx18wLAlcpqkek-Auc130_provenance.
- NP683854.RAf0ayETnpNDI8A7qUb08288-m6Yx18wLAlcpqkek-Auc130_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." NP683854.RAf0ayETnpNDI8A7qUb08288-m6Yx18wLAlcpqkek-Auc130_provenance.
- NP683854.RAf0ayETnpNDI8A7qUb08288-m6Yx18wLAlcpqkek-Auc130_assertion evidence source_evidence_literature NP683854.RAf0ayETnpNDI8A7qUb08288-m6Yx18wLAlcpqkek-Auc130_provenance.
- NP683854.RAf0ayETnpNDI8A7qUb08288-m6Yx18wLAlcpqkek-Auc130_assertion SIO_000772 18479388 NP683854.RAf0ayETnpNDI8A7qUb08288-m6Yx18wLAlcpqkek-Auc130_provenance.
- NP683854.RAf0ayETnpNDI8A7qUb08288-m6Yx18wLAlcpqkek-Auc130_assertion wasDerivedFrom befree-20140225 NP683854.RAf0ayETnpNDI8A7qUb08288-m6Yx18wLAlcpqkek-Auc130_provenance.
- NP683854.RAf0ayETnpNDI8A7qUb08288-m6Yx18wLAlcpqkek-Auc130_assertion wasGeneratedBy ECO_0000203 NP683854.RAf0ayETnpNDI8A7qUb08288-m6Yx18wLAlcpqkek-Auc130_provenance.
- befree-20140225 importedOn "2014-02-25" NP683854.RAf0ayETnpNDI8A7qUb08288-m6Yx18wLAlcpqkek-Auc130_provenance.