Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP745425.RAv4T6zI76P2_MlOHcCTCqaLQHDt_JYfu7rsWtf7KweZw130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP745425.RAv4T6zI76P2_MlOHcCTCqaLQHDt_JYfu7rsWtf7KweZw130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP745425.RAv4T6zI76P2_MlOHcCTCqaLQHDt_JYfu7rsWtf7KweZw130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP745425.RAv4T6zI76P2_MlOHcCTCqaLQHDt_JYfu7rsWtf7KweZw130_provenance.
- NP745425.RAv4T6zI76P2_MlOHcCTCqaLQHDt_JYfu7rsWtf7KweZw130_assertion description "[(2) SCN1A testing should be considered in people with possible DS where the typical initial presentation is of a developmentally normal infant presenting with recurrent, febrile or afebrile prolonged, hemiclonic seizures or generalized status epilepticus.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP745425.RAv4T6zI76P2_MlOHcCTCqaLQHDt_JYfu7rsWtf7KweZw130_provenance.
- NP745425.RAv4T6zI76P2_MlOHcCTCqaLQHDt_JYfu7rsWtf7KweZw130_assertion evidence source_evidence_literature NP745425.RAv4T6zI76P2_MlOHcCTCqaLQHDt_JYfu7rsWtf7KweZw130_provenance.
- NP745425.RAv4T6zI76P2_MlOHcCTCqaLQHDt_JYfu7rsWtf7KweZw130_assertion SIO_000772 23586701 NP745425.RAv4T6zI76P2_MlOHcCTCqaLQHDt_JYfu7rsWtf7KweZw130_provenance.
- NP745425.RAv4T6zI76P2_MlOHcCTCqaLQHDt_JYfu7rsWtf7KweZw130_assertion wasDerivedFrom befree-20140225 NP745425.RAv4T6zI76P2_MlOHcCTCqaLQHDt_JYfu7rsWtf7KweZw130_provenance.
- NP745425.RAv4T6zI76P2_MlOHcCTCqaLQHDt_JYfu7rsWtf7KweZw130_assertion wasGeneratedBy ECO_0000203 NP745425.RAv4T6zI76P2_MlOHcCTCqaLQHDt_JYfu7rsWtf7KweZw130_provenance.
- befree-20140225 importedOn "2014-02-25" NP745425.RAv4T6zI76P2_MlOHcCTCqaLQHDt_JYfu7rsWtf7KweZw130_provenance.