Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP102512.RA2pC-okvX1DUyUliDsCuRHvgpDyLbfeIqATh-sz_ZmOU130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP102512.RA2pC-okvX1DUyUliDsCuRHvgpDyLbfeIqATh-sz_ZmOU130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP102512.RA2pC-okvX1DUyUliDsCuRHvgpDyLbfeIqATh-sz_ZmOU130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP102512.RA2pC-okvX1DUyUliDsCuRHvgpDyLbfeIqATh-sz_ZmOU130_provenance.
- NP102512.RA2pC-okvX1DUyUliDsCuRHvgpDyLbfeIqATh-sz_ZmOU130_assertion description "[Allelic association of a truncation mutation of the KCNMB3 gene with idiopathic generalized epilepsy.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP102512.RA2pC-okvX1DUyUliDsCuRHvgpDyLbfeIqATh-sz_ZmOU130_provenance.
- NP102512.RA2pC-okvX1DUyUliDsCuRHvgpDyLbfeIqATh-sz_ZmOU130_assertion evidence source_evidence_literature NP102512.RA2pC-okvX1DUyUliDsCuRHvgpDyLbfeIqATh-sz_ZmOU130_provenance.
- NP102512.RA2pC-okvX1DUyUliDsCuRHvgpDyLbfeIqATh-sz_ZmOU130_assertion SIO_000772 16958040 NP102512.RA2pC-okvX1DUyUliDsCuRHvgpDyLbfeIqATh-sz_ZmOU130_provenance.
- NP102512.RA2pC-okvX1DUyUliDsCuRHvgpDyLbfeIqATh-sz_ZmOU130_assertion wasDerivedFrom gad-20150221 NP102512.RA2pC-okvX1DUyUliDsCuRHvgpDyLbfeIqATh-sz_ZmOU130_provenance.
- NP102512.RA2pC-okvX1DUyUliDsCuRHvgpDyLbfeIqATh-sz_ZmOU130_assertion wasGeneratedBy ECO_0000203 NP102512.RA2pC-okvX1DUyUliDsCuRHvgpDyLbfeIqATh-sz_ZmOU130_provenance.
- gad-20150221 importedOn "2015-02-21" NP102512.RA2pC-okvX1DUyUliDsCuRHvgpDyLbfeIqATh-sz_ZmOU130_provenance.