Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP276309.RA_KPvxmoa2dyzGicd9ghmnIbz3pPWI6n3DhDKYf7Q7s4130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP276309.RA_KPvxmoa2dyzGicd9ghmnIbz3pPWI6n3DhDKYf7Q7s4130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP276309.RA_KPvxmoa2dyzGicd9ghmnIbz3pPWI6n3DhDKYf7Q7s4130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP276309.RA_KPvxmoa2dyzGicd9ghmnIbz3pPWI6n3DhDKYf7Q7s4130_provenance.
- NP276309.RA_KPvxmoa2dyzGicd9ghmnIbz3pPWI6n3DhDKYf7Q7s4130_assertion description "[Microsatellite markers linked to juvenile myoclonic epilepsy (EJM1), benign neonatal familial convulsions EBN1 and EBN2, autosomal dominant nocturnal frontal lobe epilepsy (ADNFLE), idiopathic generalized epilepsy (EGI), progressive myoclonic epilepsy of Unverricht-Lundborg (EPM1), and partial epilepsy with auditory features (EPT), were also excluded as potential loci linked to the FC trait in our families.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP276309.RA_KPvxmoa2dyzGicd9ghmnIbz3pPWI6n3DhDKYf7Q7s4130_provenance.
- NP276309.RA_KPvxmoa2dyzGicd9ghmnIbz3pPWI6n3DhDKYf7Q7s4130_assertion evidence source_evidence_literature NP276309.RA_KPvxmoa2dyzGicd9ghmnIbz3pPWI6n3DhDKYf7Q7s4130_provenance.
- NP276309.RA_KPvxmoa2dyzGicd9ghmnIbz3pPWI6n3DhDKYf7Q7s4130_assertion SIO_000772 10691109 NP276309.RA_KPvxmoa2dyzGicd9ghmnIbz3pPWI6n3DhDKYf7Q7s4130_provenance.
- NP276309.RA_KPvxmoa2dyzGicd9ghmnIbz3pPWI6n3DhDKYf7Q7s4130_assertion wasDerivedFrom befree-2016 NP276309.RA_KPvxmoa2dyzGicd9ghmnIbz3pPWI6n3DhDKYf7Q7s4130_provenance.
- NP276309.RA_KPvxmoa2dyzGicd9ghmnIbz3pPWI6n3DhDKYf7Q7s4130_assertion wasGeneratedBy ECO_0000203 NP276309.RA_KPvxmoa2dyzGicd9ghmnIbz3pPWI6n3DhDKYf7Q7s4130_provenance.
- befree-2016 importedOn "2016-02-19" NP276309.RA_KPvxmoa2dyzGicd9ghmnIbz3pPWI6n3DhDKYf7Q7s4130_provenance.