Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP884058.RApPCJPfVH4iAKgRciqhZ_CFZzdtOxmmFbO6PWHrhzTYA130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP884058.RApPCJPfVH4iAKgRciqhZ_CFZzdtOxmmFbO6PWHrhzTYA130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP884058.RApPCJPfVH4iAKgRciqhZ_CFZzdtOxmmFbO6PWHrhzTYA130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP884058.RApPCJPfVH4iAKgRciqhZ_CFZzdtOxmmFbO6PWHrhzTYA130_provenance.
- NP884058.RApPCJPfVH4iAKgRciqhZ_CFZzdtOxmmFbO6PWHrhzTYA130_assertion description "[In this study, we performed a mutational screening of KCNJ10 in 52 patients with epilepsy of unknown cause associated with impairment of either cognitive or communicative abilities, or both.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP884058.RApPCJPfVH4iAKgRciqhZ_CFZzdtOxmmFbO6PWHrhzTYA130_provenance.
- NP884058.RApPCJPfVH4iAKgRciqhZ_CFZzdtOxmmFbO6PWHrhzTYA130_assertion evidence source_evidence_literature NP884058.RApPCJPfVH4iAKgRciqhZ_CFZzdtOxmmFbO6PWHrhzTYA130_provenance.
- NP884058.RApPCJPfVH4iAKgRciqhZ_CFZzdtOxmmFbO6PWHrhzTYA130_assertion SIO_000772 21458570 NP884058.RApPCJPfVH4iAKgRciqhZ_CFZzdtOxmmFbO6PWHrhzTYA130_provenance.
- NP884058.RApPCJPfVH4iAKgRciqhZ_CFZzdtOxmmFbO6PWHrhzTYA130_assertion wasDerivedFrom befree-2016 NP884058.RApPCJPfVH4iAKgRciqhZ_CFZzdtOxmmFbO6PWHrhzTYA130_provenance.
- NP884058.RApPCJPfVH4iAKgRciqhZ_CFZzdtOxmmFbO6PWHrhzTYA130_assertion wasGeneratedBy ECO_0000203 NP884058.RApPCJPfVH4iAKgRciqhZ_CFZzdtOxmmFbO6PWHrhzTYA130_provenance.
- befree-2016 importedOn "2016-02-19" NP884058.RApPCJPfVH4iAKgRciqhZ_CFZzdtOxmmFbO6PWHrhzTYA130_provenance.