Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP428617.RAGjy6xwE1CJnZy6XgSRt-LYxZ6O_J6xm2S-KikIrZgzY130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP428617.RAGjy6xwE1CJnZy6XgSRt-LYxZ6O_J6xm2S-KikIrZgzY130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP428617.RAGjy6xwE1CJnZy6XgSRt-LYxZ6O_J6xm2S-KikIrZgzY130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP428617.RAGjy6xwE1CJnZy6XgSRt-LYxZ6O_J6xm2S-KikIrZgzY130_provenance.
- NP428617.RAGjy6xwE1CJnZy6XgSRt-LYxZ6O_J6xm2S-KikIrZgzY130_assertion description "[This combination of early infantile spasms followed by a complex movement disorder contributes further to extent the pleiotropy of the ARX-linked `interneuronopathy` and should lead the clinician to ARX mutation screening.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP428617.RAGjy6xwE1CJnZy6XgSRt-LYxZ6O_J6xm2S-KikIrZgzY130_provenance.
- NP428617.RAGjy6xwE1CJnZy6XgSRt-LYxZ6O_J6xm2S-KikIrZgzY130_assertion evidence source_evidence_literature NP428617.RAGjy6xwE1CJnZy6XgSRt-LYxZ6O_J6xm2S-KikIrZgzY130_provenance.
- NP428617.RAGjy6xwE1CJnZy6XgSRt-LYxZ6O_J6xm2S-KikIrZgzY130_assertion SIO_000772 18468866 NP428617.RAGjy6xwE1CJnZy6XgSRt-LYxZ6O_J6xm2S-KikIrZgzY130_provenance.
- NP428617.RAGjy6xwE1CJnZy6XgSRt-LYxZ6O_J6xm2S-KikIrZgzY130_assertion wasDerivedFrom befree-20140225 NP428617.RAGjy6xwE1CJnZy6XgSRt-LYxZ6O_J6xm2S-KikIrZgzY130_provenance.
- NP428617.RAGjy6xwE1CJnZy6XgSRt-LYxZ6O_J6xm2S-KikIrZgzY130_assertion wasGeneratedBy ECO_0000203 NP428617.RAGjy6xwE1CJnZy6XgSRt-LYxZ6O_J6xm2S-KikIrZgzY130_provenance.
- befree-20140225 importedOn "2014-02-25" NP428617.RAGjy6xwE1CJnZy6XgSRt-LYxZ6O_J6xm2S-KikIrZgzY130_provenance.