Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP682351.RAtAi1EyA2YW1nKaXOQ3d2zjB45HsHeDxKvD6vrqTG598130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP682351.RAtAi1EyA2YW1nKaXOQ3d2zjB45HsHeDxKvD6vrqTG598130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP682351.RAtAi1EyA2YW1nKaXOQ3d2zjB45HsHeDxKvD6vrqTG598130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP682351.RAtAi1EyA2YW1nKaXOQ3d2zjB45HsHeDxKvD6vrqTG598130_provenance.
- befree-20150227 importedOn "2015-02-27" NP682351.RAtAi1EyA2YW1nKaXOQ3d2zjB45HsHeDxKvD6vrqTG598130_provenance.
- NP682351.RAtAi1EyA2YW1nKaXOQ3d2zjB45HsHeDxKvD6vrqTG598130_assertion wasGeneratedBy ECO_0000203 NP682351.RAtAi1EyA2YW1nKaXOQ3d2zjB45HsHeDxKvD6vrqTG598130_provenance.
- NP682351.RAtAi1EyA2YW1nKaXOQ3d2zjB45HsHeDxKvD6vrqTG598130_assertion wasDerivedFrom befree-20150227 NP682351.RAtAi1EyA2YW1nKaXOQ3d2zjB45HsHeDxKvD6vrqTG598130_provenance.
- NP682351.RAtAi1EyA2YW1nKaXOQ3d2zjB45HsHeDxKvD6vrqTG598130_assertion SIO_000772 12610651 NP682351.RAtAi1EyA2YW1nKaXOQ3d2zjB45HsHeDxKvD6vrqTG598130_provenance.
- NP682351.RAtAi1EyA2YW1nKaXOQ3d2zjB45HsHeDxKvD6vrqTG598130_assertion evidence source_evidence_literature NP682351.RAtAi1EyA2YW1nKaXOQ3d2zjB45HsHeDxKvD6vrqTG598130_provenance.
- NP682351.RAtAi1EyA2YW1nKaXOQ3d2zjB45HsHeDxKvD6vrqTG598130_assertion description "[R542Q in SCN1A was observed in one autism family and had previously been identified in a patient with juvenile myoclonic epilepsy.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP682351.RAtAi1EyA2YW1nKaXOQ3d2zjB45HsHeDxKvD6vrqTG598130_provenance.