Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP758225.RAhff_9OTyjdV4xXXlp_N0i3YZVf-yPFbyJtc-mzBAuXo130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP758225.RAhff_9OTyjdV4xXXlp_N0i3YZVf-yPFbyJtc-mzBAuXo130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP758225.RAhff_9OTyjdV4xXXlp_N0i3YZVf-yPFbyJtc-mzBAuXo130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP758225.RAhff_9OTyjdV4xXXlp_N0i3YZVf-yPFbyJtc-mzBAuXo130_provenance.
- NP758225.RAhff_9OTyjdV4xXXlp_N0i3YZVf-yPFbyJtc-mzBAuXo130_assertion description "[A high frequency of epilepsy (43%) was observed in our patients with GLUD1 mutations.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP758225.RAhff_9OTyjdV4xXXlp_N0i3YZVf-yPFbyJtc-mzBAuXo130_provenance.
- NP758225.RAhff_9OTyjdV4xXXlp_N0i3YZVf-yPFbyJtc-mzBAuXo130_assertion evidence source_evidence_literature NP758225.RAhff_9OTyjdV4xXXlp_N0i3YZVf-yPFbyJtc-mzBAuXo130_provenance.
- NP758225.RAhff_9OTyjdV4xXXlp_N0i3YZVf-yPFbyJtc-mzBAuXo130_assertion SIO_000772 19690084 NP758225.RAhff_9OTyjdV4xXXlp_N0i3YZVf-yPFbyJtc-mzBAuXo130_provenance.
- NP758225.RAhff_9OTyjdV4xXXlp_N0i3YZVf-yPFbyJtc-mzBAuXo130_assertion wasDerivedFrom befree-2016 NP758225.RAhff_9OTyjdV4xXXlp_N0i3YZVf-yPFbyJtc-mzBAuXo130_provenance.
- NP758225.RAhff_9OTyjdV4xXXlp_N0i3YZVf-yPFbyJtc-mzBAuXo130_assertion wasGeneratedBy ECO_0000203 NP758225.RAhff_9OTyjdV4xXXlp_N0i3YZVf-yPFbyJtc-mzBAuXo130_provenance.
- befree-2016 importedOn "2016-02-19" NP758225.RAhff_9OTyjdV4xXXlp_N0i3YZVf-yPFbyJtc-mzBAuXo130_provenance.