Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP206447.RAU0giq2p7htmZyLL8n2UPytdT6R_MLKNewRbMf_i_K30130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP206447.RAU0giq2p7htmZyLL8n2UPytdT6R_MLKNewRbMf_i_K30130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP206447.RAU0giq2p7htmZyLL8n2UPytdT6R_MLKNewRbMf_i_K30130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP206447.RAU0giq2p7htmZyLL8n2UPytdT6R_MLKNewRbMf_i_K30130_provenance.
- NP206447.RAU0giq2p7htmZyLL8n2UPytdT6R_MLKNewRbMf_i_K30130_assertion wasGeneratedBy ECO_0000203 NP206447.RAU0giq2p7htmZyLL8n2UPytdT6R_MLKNewRbMf_i_K30130_provenance.
- NP206447.RAU0giq2p7htmZyLL8n2UPytdT6R_MLKNewRbMf_i_K30130_assertion wasDerivedFrom befree-20140225 NP206447.RAU0giq2p7htmZyLL8n2UPytdT6R_MLKNewRbMf_i_K30130_provenance.
- NP206447.RAU0giq2p7htmZyLL8n2UPytdT6R_MLKNewRbMf_i_K30130_assertion SIO_000772 21114141 NP206447.RAU0giq2p7htmZyLL8n2UPytdT6R_MLKNewRbMf_i_K30130_provenance.
- NP206447.RAU0giq2p7htmZyLL8n2UPytdT6R_MLKNewRbMf_i_K30130_assertion evidence source_evidence_literature NP206447.RAU0giq2p7htmZyLL8n2UPytdT6R_MLKNewRbMf_i_K30130_provenance.
- NP206447.RAU0giq2p7htmZyLL8n2UPytdT6R_MLKNewRbMf_i_K30130_assertion description "[A novel de novo SCN1A missense mutation in Severe Myoclonic Epilepsy Borderland.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP206447.RAU0giq2p7htmZyLL8n2UPytdT6R_MLKNewRbMf_i_K30130_provenance.
- befree-20140225 importedOn "2014-02-25" NP206447.RAU0giq2p7htmZyLL8n2UPytdT6R_MLKNewRbMf_i_K30130_provenance.