Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP280908.RAbi47Ee3bQ1tclOU2OI6DG10aKi3X_2wANIP9UEp1OEo130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP280908.RAbi47Ee3bQ1tclOU2OI6DG10aKi3X_2wANIP9UEp1OEo130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP280908.RAbi47Ee3bQ1tclOU2OI6DG10aKi3X_2wANIP9UEp1OEo130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP280908.RAbi47Ee3bQ1tclOU2OI6DG10aKi3X_2wANIP9UEp1OEo130_provenance.
- NP280908.RAbi47Ee3bQ1tclOU2OI6DG10aKi3X_2wANIP9UEp1OEo130_assertion description "[To determine the role of the calcium-channel beta4-subunit gene CACNB4 on chromosome 2q22-23 in related human disorders, we screened for mutations in small pedigrees with familial epilepsy and ataxia.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP280908.RAbi47Ee3bQ1tclOU2OI6DG10aKi3X_2wANIP9UEp1OEo130_provenance.
- NP280908.RAbi47Ee3bQ1tclOU2OI6DG10aKi3X_2wANIP9UEp1OEo130_assertion evidence source_evidence_literature NP280908.RAbi47Ee3bQ1tclOU2OI6DG10aKi3X_2wANIP9UEp1OEo130_provenance.
- NP280908.RAbi47Ee3bQ1tclOU2OI6DG10aKi3X_2wANIP9UEp1OEo130_assertion SIO_000772 10762541 NP280908.RAbi47Ee3bQ1tclOU2OI6DG10aKi3X_2wANIP9UEp1OEo130_provenance.
- NP280908.RAbi47Ee3bQ1tclOU2OI6DG10aKi3X_2wANIP9UEp1OEo130_assertion wasDerivedFrom befree-2016 NP280908.RAbi47Ee3bQ1tclOU2OI6DG10aKi3X_2wANIP9UEp1OEo130_provenance.
- NP280908.RAbi47Ee3bQ1tclOU2OI6DG10aKi3X_2wANIP9UEp1OEo130_assertion wasGeneratedBy ECO_0000203 NP280908.RAbi47Ee3bQ1tclOU2OI6DG10aKi3X_2wANIP9UEp1OEo130_provenance.
- befree-2016 importedOn "2016-02-19" NP280908.RAbi47Ee3bQ1tclOU2OI6DG10aKi3X_2wANIP9UEp1OEo130_provenance.