Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP314280.RAYcdu7sf78H7DCwKY8d5Z2PyS2Xj39MFQ1as1AxmGmiw130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP314280.RAYcdu7sf78H7DCwKY8d5Z2PyS2Xj39MFQ1as1AxmGmiw130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP314280.RAYcdu7sf78H7DCwKY8d5Z2PyS2Xj39MFQ1as1AxmGmiw130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP314280.RAYcdu7sf78H7DCwKY8d5Z2PyS2Xj39MFQ1as1AxmGmiw130_provenance.
- NP314280.RAYcdu7sf78H7DCwKY8d5Z2PyS2Xj39MFQ1as1AxmGmiw130_assertion description "[Susceptibility genes for two syndromes of idiopathic generalized epilepsies, the benign familial neonatal convulsions and juvenile myoclonic epilepsy, have been assigned to the chromosomal regions 20q13 (EBN1), 8q24 (EBN2) and 6p21 (EJM1).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP314280.RAYcdu7sf78H7DCwKY8d5Z2PyS2Xj39MFQ1as1AxmGmiw130_provenance.
- NP314280.RAYcdu7sf78H7DCwKY8d5Z2PyS2Xj39MFQ1as1AxmGmiw130_assertion evidence source_evidence_literature NP314280.RAYcdu7sf78H7DCwKY8d5Z2PyS2Xj39MFQ1as1AxmGmiw130_provenance.
- NP314280.RAYcdu7sf78H7DCwKY8d5Z2PyS2Xj39MFQ1as1AxmGmiw130_assertion SIO_000772 8796880 NP314280.RAYcdu7sf78H7DCwKY8d5Z2PyS2Xj39MFQ1as1AxmGmiw130_provenance.
- NP314280.RAYcdu7sf78H7DCwKY8d5Z2PyS2Xj39MFQ1as1AxmGmiw130_assertion wasDerivedFrom befree-20150227 NP314280.RAYcdu7sf78H7DCwKY8d5Z2PyS2Xj39MFQ1as1AxmGmiw130_provenance.
- NP314280.RAYcdu7sf78H7DCwKY8d5Z2PyS2Xj39MFQ1as1AxmGmiw130_assertion wasGeneratedBy ECO_0000203 NP314280.RAYcdu7sf78H7DCwKY8d5Z2PyS2Xj39MFQ1as1AxmGmiw130_provenance.
- befree-20150227 importedOn "2015-02-27" NP314280.RAYcdu7sf78H7DCwKY8d5Z2PyS2Xj39MFQ1as1AxmGmiw130_provenance.