Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP415744.RAg4mw8YK_Ee-Sxkx3hHz_VUDs_LKA--F5aHjndMIoDk4130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP415744.RAg4mw8YK_Ee-Sxkx3hHz_VUDs_LKA--F5aHjndMIoDk4130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP415744.RAg4mw8YK_Ee-Sxkx3hHz_VUDs_LKA--F5aHjndMIoDk4130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP415744.RAg4mw8YK_Ee-Sxkx3hHz_VUDs_LKA--F5aHjndMIoDk4130_provenance.
- NP415744.RAg4mw8YK_Ee-Sxkx3hHz_VUDs_LKA--F5aHjndMIoDk4130_assertion description "[Loss of CSTB function due to mutations is consistent with the observed neurodegenerative pathology and phenotype, but the functional link to the epileptic phenotype of EPM1 remains largely unknown.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP415744.RAg4mw8YK_Ee-Sxkx3hHz_VUDs_LKA--F5aHjndMIoDk4130_provenance.
- NP415744.RAg4mw8YK_Ee-Sxkx3hHz_VUDs_LKA--F5aHjndMIoDk4130_assertion evidence source_evidence_literature NP415744.RAg4mw8YK_Ee-Sxkx3hHz_VUDs_LKA--F5aHjndMIoDk4130_provenance.
- NP415744.RAg4mw8YK_Ee-Sxkx3hHz_VUDs_LKA--F5aHjndMIoDk4130_assertion SIO_000772 14526183 NP415744.RAg4mw8YK_Ee-Sxkx3hHz_VUDs_LKA--F5aHjndMIoDk4130_provenance.
- NP415744.RAg4mw8YK_Ee-Sxkx3hHz_VUDs_LKA--F5aHjndMIoDk4130_assertion wasDerivedFrom befree-2016 NP415744.RAg4mw8YK_Ee-Sxkx3hHz_VUDs_LKA--F5aHjndMIoDk4130_provenance.
- NP415744.RAg4mw8YK_Ee-Sxkx3hHz_VUDs_LKA--F5aHjndMIoDk4130_assertion wasGeneratedBy ECO_0000203 NP415744.RAg4mw8YK_Ee-Sxkx3hHz_VUDs_LKA--F5aHjndMIoDk4130_provenance.
- befree-2016 importedOn "2016-02-19" NP415744.RAg4mw8YK_Ee-Sxkx3hHz_VUDs_LKA--F5aHjndMIoDk4130_provenance.