Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP656541.RAwAIXoPL-0he3SsSuE6C7MkI7N98hlwBZlsJp3HHg1So130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP656541.RAwAIXoPL-0he3SsSuE6C7MkI7N98hlwBZlsJp3HHg1So130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP656541.RAwAIXoPL-0he3SsSuE6C7MkI7N98hlwBZlsJp3HHg1So130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP656541.RAwAIXoPL-0he3SsSuE6C7MkI7N98hlwBZlsJp3HHg1So130_provenance.
- NP656541.RAwAIXoPL-0he3SsSuE6C7MkI7N98hlwBZlsJp3HHg1So130_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." NP656541.RAwAIXoPL-0he3SsSuE6C7MkI7N98hlwBZlsJp3HHg1So130_provenance.
- NP656541.RAwAIXoPL-0he3SsSuE6C7MkI7N98hlwBZlsJp3HHg1So130_assertion evidence source_evidence_literature NP656541.RAwAIXoPL-0he3SsSuE6C7MkI7N98hlwBZlsJp3HHg1So130_provenance.
- NP656541.RAwAIXoPL-0he3SsSuE6C7MkI7N98hlwBZlsJp3HHg1So130_assertion SIO_000772 8796880 NP656541.RAwAIXoPL-0he3SsSuE6C7MkI7N98hlwBZlsJp3HHg1So130_provenance.
- NP656541.RAwAIXoPL-0he3SsSuE6C7MkI7N98hlwBZlsJp3HHg1So130_assertion wasDerivedFrom befree-20140225 NP656541.RAwAIXoPL-0he3SsSuE6C7MkI7N98hlwBZlsJp3HHg1So130_provenance.
- NP656541.RAwAIXoPL-0he3SsSuE6C7MkI7N98hlwBZlsJp3HHg1So130_assertion wasGeneratedBy ECO_0000203 NP656541.RAwAIXoPL-0he3SsSuE6C7MkI7N98hlwBZlsJp3HHg1So130_provenance.
- befree-20140225 importedOn "2014-02-25" NP656541.RAwAIXoPL-0he3SsSuE6C7MkI7N98hlwBZlsJp3HHg1So130_provenance.