Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP758657.RA510GtbzYANbe-214IFtR6r3Drd1shtkgTXL7ztF2l1E130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP758657.RA510GtbzYANbe-214IFtR6r3Drd1shtkgTXL7ztF2l1E130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP758657.RA510GtbzYANbe-214IFtR6r3Drd1shtkgTXL7ztF2l1E130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP758657.RA510GtbzYANbe-214IFtR6r3Drd1shtkgTXL7ztF2l1E130_provenance.
- NP758657.RA510GtbzYANbe-214IFtR6r3Drd1shtkgTXL7ztF2l1E130_assertion description "[Two apparent exceptions to this rule are the MASS1 gene, which is mutated in the Frings mouse model of audiogenic epilepsy, and the LGI1 gene, which is mutated in autosomal dominant partial epilepsy with auditory features (ADPEAF).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP758657.RA510GtbzYANbe-214IFtR6r3Drd1shtkgTXL7ztF2l1E130_provenance.
- NP758657.RA510GtbzYANbe-214IFtR6r3Drd1shtkgTXL7ztF2l1E130_assertion evidence source_evidence_literature NP758657.RA510GtbzYANbe-214IFtR6r3Drd1shtkgTXL7ztF2l1E130_provenance.
- NP758657.RA510GtbzYANbe-214IFtR6r3Drd1shtkgTXL7ztF2l1E130_assertion SIO_000772 12095917 NP758657.RA510GtbzYANbe-214IFtR6r3Drd1shtkgTXL7ztF2l1E130_provenance.
- NP758657.RA510GtbzYANbe-214IFtR6r3Drd1shtkgTXL7ztF2l1E130_assertion wasDerivedFrom befree-20140225 NP758657.RA510GtbzYANbe-214IFtR6r3Drd1shtkgTXL7ztF2l1E130_provenance.
- NP758657.RA510GtbzYANbe-214IFtR6r3Drd1shtkgTXL7ztF2l1E130_assertion wasGeneratedBy ECO_0000203 NP758657.RA510GtbzYANbe-214IFtR6r3Drd1shtkgTXL7ztF2l1E130_provenance.
- befree-20140225 importedOn "2014-02-25" NP758657.RA510GtbzYANbe-214IFtR6r3Drd1shtkgTXL7ztF2l1E130_provenance.