Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP838032.RAejNhCdWpvHtxpqe28TEFjTK_DjM69jDM-zNOEqaMs74130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP838032.RAejNhCdWpvHtxpqe28TEFjTK_DjM69jDM-zNOEqaMs74130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP838032.RAejNhCdWpvHtxpqe28TEFjTK_DjM69jDM-zNOEqaMs74130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP838032.RAejNhCdWpvHtxpqe28TEFjTK_DjM69jDM-zNOEqaMs74130_provenance.
- NP838032.RAejNhCdWpvHtxpqe28TEFjTK_DjM69jDM-zNOEqaMs74130_assertion description "[Mutations in TNK2 in severe autosomal recessive infantile onset epilepsy.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP838032.RAejNhCdWpvHtxpqe28TEFjTK_DjM69jDM-zNOEqaMs74130_provenance.
- NP838032.RAejNhCdWpvHtxpqe28TEFjTK_DjM69jDM-zNOEqaMs74130_assertion evidence source_evidence_literature NP838032.RAejNhCdWpvHtxpqe28TEFjTK_DjM69jDM-zNOEqaMs74130_provenance.
- NP838032.RAejNhCdWpvHtxpqe28TEFjTK_DjM69jDM-zNOEqaMs74130_assertion SIO_000772 23686771 NP838032.RAejNhCdWpvHtxpqe28TEFjTK_DjM69jDM-zNOEqaMs74130_provenance.
- NP838032.RAejNhCdWpvHtxpqe28TEFjTK_DjM69jDM-zNOEqaMs74130_assertion wasDerivedFrom befree-20150227 NP838032.RAejNhCdWpvHtxpqe28TEFjTK_DjM69jDM-zNOEqaMs74130_provenance.
- NP838032.RAejNhCdWpvHtxpqe28TEFjTK_DjM69jDM-zNOEqaMs74130_assertion wasGeneratedBy ECO_0000203 NP838032.RAejNhCdWpvHtxpqe28TEFjTK_DjM69jDM-zNOEqaMs74130_provenance.
- befree-20150227 importedOn "2015-02-27" NP838032.RAejNhCdWpvHtxpqe28TEFjTK_DjM69jDM-zNOEqaMs74130_provenance.