Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP813935.RAhg7s4ZtsZ7YI1PP_12e4ZH1OTCgjzLbFc3CCuzc7-R8130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP813935.RAhg7s4ZtsZ7YI1PP_12e4ZH1OTCgjzLbFc3CCuzc7-R8130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP813935.RAhg7s4ZtsZ7YI1PP_12e4ZH1OTCgjzLbFc3CCuzc7-R8130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP813935.RAhg7s4ZtsZ7YI1PP_12e4ZH1OTCgjzLbFc3CCuzc7-R8130_provenance.
- NP813935.RAhg7s4ZtsZ7YI1PP_12e4ZH1OTCgjzLbFc3CCuzc7-R8130_assertion description "[These findings suggest that pathological aggregation of alpha/beta spectrin heterodimers and abnormal AIS integrity resulting from SPTAN1 mutations were involved in pathogenesis of infantile epilepsy.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP813935.RAhg7s4ZtsZ7YI1PP_12e4ZH1OTCgjzLbFc3CCuzc7-R8130_provenance.
- NP813935.RAhg7s4ZtsZ7YI1PP_12e4ZH1OTCgjzLbFc3CCuzc7-R8130_assertion evidence source_evidence_literature NP813935.RAhg7s4ZtsZ7YI1PP_12e4ZH1OTCgjzLbFc3CCuzc7-R8130_provenance.
- NP813935.RAhg7s4ZtsZ7YI1PP_12e4ZH1OTCgjzLbFc3CCuzc7-R8130_assertion SIO_000772 20493457 NP813935.RAhg7s4ZtsZ7YI1PP_12e4ZH1OTCgjzLbFc3CCuzc7-R8130_provenance.
- NP813935.RAhg7s4ZtsZ7YI1PP_12e4ZH1OTCgjzLbFc3CCuzc7-R8130_assertion wasDerivedFrom befree-2016 NP813935.RAhg7s4ZtsZ7YI1PP_12e4ZH1OTCgjzLbFc3CCuzc7-R8130_provenance.
- NP813935.RAhg7s4ZtsZ7YI1PP_12e4ZH1OTCgjzLbFc3CCuzc7-R8130_assertion wasGeneratedBy ECO_0000203 NP813935.RAhg7s4ZtsZ7YI1PP_12e4ZH1OTCgjzLbFc3CCuzc7-R8130_provenance.
- befree-2016 importedOn "2016-02-19" NP813935.RAhg7s4ZtsZ7YI1PP_12e4ZH1OTCgjzLbFc3CCuzc7-R8130_provenance.