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- source_evidence_literature type ECO_0000212 NP978147.RANIA_kB-1tlT_NhkzVJSVIg-CrTq_XeYxEz-EOdfaxuY130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP978147.RANIA_kB-1tlT_NhkzVJSVIg-CrTq_XeYxEz-EOdfaxuY130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP978147.RANIA_kB-1tlT_NhkzVJSVIg-CrTq_XeYxEz-EOdfaxuY130_provenance.
- NP978147.RANIA_kB-1tlT_NhkzVJSVIg-CrTq_XeYxEz-EOdfaxuY130_assertion description "[Brain magnetic resonance imaging (MRI) of all patients showed no brain malformations in contrast to the patients with a premature termination mutation in other exons of ARX.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP978147.RANIA_kB-1tlT_NhkzVJSVIg-CrTq_XeYxEz-EOdfaxuY130_provenance.
- NP978147.RANIA_kB-1tlT_NhkzVJSVIg-CrTq_XeYxEz-EOdfaxuY130_assertion evidence source_evidence_literature NP978147.RANIA_kB-1tlT_NhkzVJSVIg-CrTq_XeYxEz-EOdfaxuY130_provenance.
- NP978147.RANIA_kB-1tlT_NhkzVJSVIg-CrTq_XeYxEz-EOdfaxuY130_assertion SIO_000772 20384723 NP978147.RANIA_kB-1tlT_NhkzVJSVIg-CrTq_XeYxEz-EOdfaxuY130_provenance.
- NP978147.RANIA_kB-1tlT_NhkzVJSVIg-CrTq_XeYxEz-EOdfaxuY130_assertion wasDerivedFrom befree-20150227 NP978147.RANIA_kB-1tlT_NhkzVJSVIg-CrTq_XeYxEz-EOdfaxuY130_provenance.
- NP978147.RANIA_kB-1tlT_NhkzVJSVIg-CrTq_XeYxEz-EOdfaxuY130_assertion wasGeneratedBy ECO_0000203 NP978147.RANIA_kB-1tlT_NhkzVJSVIg-CrTq_XeYxEz-EOdfaxuY130_provenance.
- befree-20150227 importedOn "2015-02-27" NP978147.RANIA_kB-1tlT_NhkzVJSVIg-CrTq_XeYxEz-EOdfaxuY130_provenance.