Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP932050.RADgaLmIQhEsRDDAZ7TY8pnDERC9V8194a3w7mFjsGi0M130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP932050.RADgaLmIQhEsRDDAZ7TY8pnDERC9V8194a3w7mFjsGi0M130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP932050.RADgaLmIQhEsRDDAZ7TY8pnDERC9V8194a3w7mFjsGi0M130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP932050.RADgaLmIQhEsRDDAZ7TY8pnDERC9V8194a3w7mFjsGi0M130_provenance.
- NP932050.RADgaLmIQhEsRDDAZ7TY8pnDERC9V8194a3w7mFjsGi0M130_assertion description "[They include well-recognized syndromes such as tuberous sclerosis complex, epilepsy associated with Rett syndrome, some of the progressive myoclonic epilepsies, and novel disorders such as epilepsy associated with mutations in the PCDH 19 gene.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP932050.RADgaLmIQhEsRDDAZ7TY8pnDERC9V8194a3w7mFjsGi0M130_provenance.
- NP932050.RADgaLmIQhEsRDDAZ7TY8pnDERC9V8194a3w7mFjsGi0M130_assertion evidence source_evidence_literature NP932050.RADgaLmIQhEsRDDAZ7TY8pnDERC9V8194a3w7mFjsGi0M130_provenance.
- NP932050.RADgaLmIQhEsRDDAZ7TY8pnDERC9V8194a3w7mFjsGi0M130_assertion SIO_000772 22946725 NP932050.RADgaLmIQhEsRDDAZ7TY8pnDERC9V8194a3w7mFjsGi0M130_provenance.
- NP932050.RADgaLmIQhEsRDDAZ7TY8pnDERC9V8194a3w7mFjsGi0M130_assertion wasDerivedFrom befree-20150227 NP932050.RADgaLmIQhEsRDDAZ7TY8pnDERC9V8194a3w7mFjsGi0M130_provenance.
- NP932050.RADgaLmIQhEsRDDAZ7TY8pnDERC9V8194a3w7mFjsGi0M130_assertion wasGeneratedBy ECO_0000203 NP932050.RADgaLmIQhEsRDDAZ7TY8pnDERC9V8194a3w7mFjsGi0M130_provenance.
- befree-20150227 importedOn "2015-02-27" NP932050.RADgaLmIQhEsRDDAZ7TY8pnDERC9V8194a3w7mFjsGi0M130_provenance.