Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP588288.RACWSRADsaHFqilNwds9eEfIVMnXS97l-67-FWzEMuR0A130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP588288.RACWSRADsaHFqilNwds9eEfIVMnXS97l-67-FWzEMuR0A130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP588288.RACWSRADsaHFqilNwds9eEfIVMnXS97l-67-FWzEMuR0A130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP588288.RACWSRADsaHFqilNwds9eEfIVMnXS97l-67-FWzEMuR0A130_provenance.
- NP588288.RACWSRADsaHFqilNwds9eEfIVMnXS97l-67-FWzEMuR0A130_assertion description "[Linkage analysis in separately ascertained families of probands with juvenile myoclonic epilepsy (JME) has previously provided evidence both for and against the existence of a locus (designated `EJM1`), on chromosome 6p, predisposing to a trait defined as either clinical JME, its associated electroencephalographic abnormality, or idiopathic generalized epilepsy.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP588288.RACWSRADsaHFqilNwds9eEfIVMnXS97l-67-FWzEMuR0A130_provenance.
- NP588288.RACWSRADsaHFqilNwds9eEfIVMnXS97l-67-FWzEMuR0A130_assertion evidence source_evidence_literature NP588288.RACWSRADsaHFqilNwds9eEfIVMnXS97l-67-FWzEMuR0A130_provenance.
- NP588288.RACWSRADsaHFqilNwds9eEfIVMnXS97l-67-FWzEMuR0A130_assertion SIO_000772 8751867 NP588288.RACWSRADsaHFqilNwds9eEfIVMnXS97l-67-FWzEMuR0A130_provenance.
- NP588288.RACWSRADsaHFqilNwds9eEfIVMnXS97l-67-FWzEMuR0A130_assertion wasDerivedFrom befree-20140225 NP588288.RACWSRADsaHFqilNwds9eEfIVMnXS97l-67-FWzEMuR0A130_provenance.
- NP588288.RACWSRADsaHFqilNwds9eEfIVMnXS97l-67-FWzEMuR0A130_assertion wasGeneratedBy ECO_0000203 NP588288.RACWSRADsaHFqilNwds9eEfIVMnXS97l-67-FWzEMuR0A130_provenance.
- befree-20140225 importedOn "2014-02-25" NP588288.RACWSRADsaHFqilNwds9eEfIVMnXS97l-67-FWzEMuR0A130_provenance.