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- source_evidence_literature type ECO_0000212 NP840293.RAwl6uor4c7XCEpj4n26-Jul-1du2XCO1aw4w0_oL3r_U130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP840293.RAwl6uor4c7XCEpj4n26-Jul-1du2XCO1aw4w0_oL3r_U130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP840293.RAwl6uor4c7XCEpj4n26-Jul-1du2XCO1aw4w0_oL3r_U130_provenance.
- NP840293.RAwl6uor4c7XCEpj4n26-Jul-1du2XCO1aw4w0_oL3r_U130_assertion description "[We have identified inactivating mutations in the gene BCKDK (Branched Chain Ketoacid Dehydrogenase Kinase) in consanguineous families with autism, epilepsy, and intellectual disability.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP840293.RAwl6uor4c7XCEpj4n26-Jul-1du2XCO1aw4w0_oL3r_U130_provenance.
- NP840293.RAwl6uor4c7XCEpj4n26-Jul-1du2XCO1aw4w0_oL3r_U130_assertion evidence source_evidence_literature NP840293.RAwl6uor4c7XCEpj4n26-Jul-1du2XCO1aw4w0_oL3r_U130_provenance.
- NP840293.RAwl6uor4c7XCEpj4n26-Jul-1du2XCO1aw4w0_oL3r_U130_assertion SIO_000772 22956686 NP840293.RAwl6uor4c7XCEpj4n26-Jul-1du2XCO1aw4w0_oL3r_U130_provenance.
- NP840293.RAwl6uor4c7XCEpj4n26-Jul-1du2XCO1aw4w0_oL3r_U130_assertion wasDerivedFrom befree-20150227 NP840293.RAwl6uor4c7XCEpj4n26-Jul-1du2XCO1aw4w0_oL3r_U130_provenance.
- NP840293.RAwl6uor4c7XCEpj4n26-Jul-1du2XCO1aw4w0_oL3r_U130_assertion wasGeneratedBy ECO_0000203 NP840293.RAwl6uor4c7XCEpj4n26-Jul-1du2XCO1aw4w0_oL3r_U130_provenance.
- befree-20150227 importedOn "2015-02-27" NP840293.RAwl6uor4c7XCEpj4n26-Jul-1du2XCO1aw4w0_oL3r_U130_provenance.