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- NP838032.RAejNhCdWpvHtxpqe28TEFjTK_DjM69jDM-zNOEqaMs74130_assertion type Assertion NP838032.RAejNhCdWpvHtxpqe28TEFjTK_DjM69jDM-zNOEqaMs74130_head.
- 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.