Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP414116.RAYnkPYqMs8hT0_ANqBFDtx5z2v4yIsWqeGePeTb8Znd0130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP414116.RAYnkPYqMs8hT0_ANqBFDtx5z2v4yIsWqeGePeTb8Znd0130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP414116.RAYnkPYqMs8hT0_ANqBFDtx5z2v4yIsWqeGePeTb8Znd0130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP414116.RAYnkPYqMs8hT0_ANqBFDtx5z2v4yIsWqeGePeTb8Znd0130_provenance.
- NP414116.RAYnkPYqMs8hT0_ANqBFDtx5z2v4yIsWqeGePeTb8Znd0130_assertion description "[SCN1A mutation analysis in myoclonic astatic epilepsy and severe idiopathic generalized epilepsy of infancy with generalized tonic-clonic seizures.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP414116.RAYnkPYqMs8hT0_ANqBFDtx5z2v4yIsWqeGePeTb8Znd0130_provenance.
- NP414116.RAYnkPYqMs8hT0_ANqBFDtx5z2v4yIsWqeGePeTb8Znd0130_assertion evidence source_evidence_literature NP414116.RAYnkPYqMs8hT0_ANqBFDtx5z2v4yIsWqeGePeTb8Znd0130_provenance.
- NP414116.RAYnkPYqMs8hT0_ANqBFDtx5z2v4yIsWqeGePeTb8Znd0130_assertion SIO_000772 15944908 NP414116.RAYnkPYqMs8hT0_ANqBFDtx5z2v4yIsWqeGePeTb8Znd0130_provenance.
- NP414116.RAYnkPYqMs8hT0_ANqBFDtx5z2v4yIsWqeGePeTb8Znd0130_assertion wasDerivedFrom befree-20140225 NP414116.RAYnkPYqMs8hT0_ANqBFDtx5z2v4yIsWqeGePeTb8Znd0130_provenance.
- NP414116.RAYnkPYqMs8hT0_ANqBFDtx5z2v4yIsWqeGePeTb8Znd0130_assertion wasGeneratedBy ECO_0000203 NP414116.RAYnkPYqMs8hT0_ANqBFDtx5z2v4yIsWqeGePeTb8Znd0130_provenance.
- befree-20140225 importedOn "2014-02-25" NP414116.RAYnkPYqMs8hT0_ANqBFDtx5z2v4yIsWqeGePeTb8Znd0130_provenance.