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- NP549.RAeV_rjMtNxKQ7XYr_qsnfXbOpPHZhqVEookvV4tEEGeo130_assertion type Assertion NP549.RAeV_rjMtNxKQ7XYr_qsnfXbOpPHZhqVEookvV4tEEGeo130_head.
- NP549.RAeV_rjMtNxKQ7XYr_qsnfXbOpPHZhqVEookvV4tEEGeo130_assertion wasGeneratedBy ECO_0000218 NP549.RAeV_rjMtNxKQ7XYr_qsnfXbOpPHZhqVEookvV4tEEGeo130_provenance.
- NP549.RAeV_rjMtNxKQ7XYr_qsnfXbOpPHZhqVEookvV4tEEGeo130_assertion wasDerivedFrom uniprot-20150221 NP549.RAeV_rjMtNxKQ7XYr_qsnfXbOpPHZhqVEookvV4tEEGeo130_provenance.
- NP549.RAeV_rjMtNxKQ7XYr_qsnfXbOpPHZhqVEookvV4tEEGeo130_assertion SIO_000772 12019207 NP549.RAeV_rjMtNxKQ7XYr_qsnfXbOpPHZhqVEookvV4tEEGeo130_provenance.
- NP549.RAeV_rjMtNxKQ7XYr_qsnfXbOpPHZhqVEookvV4tEEGeo130_assertion evidence source_evidence_curated NP549.RAeV_rjMtNxKQ7XYr_qsnfXbOpPHZhqVEookvV4tEEGeo130_provenance.
- NP549.RAeV_rjMtNxKQ7XYr_qsnfXbOpPHZhqVEookvV4tEEGeo130_assertion description "[Genotype-phenotype correlations for EPM2A mutations in Lafora's progressive myoclonus epilepsy: exon 1 mutations associate with an early-onset cognitive deficit subphenotype.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP549.RAeV_rjMtNxKQ7XYr_qsnfXbOpPHZhqVEookvV4tEEGeo130_provenance.