Matches in Nanopublications for { <http://rdf.disgenet.org/nanopublications.trig#NP313448.RAUoZHpzeGMAU8-Tlv47DVVb-A0-EEtc9v4xD8jXXR3Gw130_assertion> ?p ?o ?g. }
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- NP313448.RAUoZHpzeGMAU8-Tlv47DVVb-A0-EEtc9v4xD8jXXR3Gw130_assertion type Assertion NP313448.RAUoZHpzeGMAU8-Tlv47DVVb-A0-EEtc9v4xD8jXXR3Gw130_head.
- NP313448.RAUoZHpzeGMAU8-Tlv47DVVb-A0-EEtc9v4xD8jXXR3Gw130_assertion wasGeneratedBy ECO_0000203 NP313448.RAUoZHpzeGMAU8-Tlv47DVVb-A0-EEtc9v4xD8jXXR3Gw130_provenance.
- NP313448.RAUoZHpzeGMAU8-Tlv47DVVb-A0-EEtc9v4xD8jXXR3Gw130_assertion wasDerivedFrom befree-20140225 NP313448.RAUoZHpzeGMAU8-Tlv47DVVb-A0-EEtc9v4xD8jXXR3Gw130_provenance.
- NP313448.RAUoZHpzeGMAU8-Tlv47DVVb-A0-EEtc9v4xD8jXXR3Gw130_assertion SIO_000772 11739371 NP313448.RAUoZHpzeGMAU8-Tlv47DVVb-A0-EEtc9v4xD8jXXR3Gw130_provenance.
- NP313448.RAUoZHpzeGMAU8-Tlv47DVVb-A0-EEtc9v4xD8jXXR3Gw130_assertion evidence source_evidence_literature NP313448.RAUoZHpzeGMAU8-Tlv47DVVb-A0-EEtc9v4xD8jXXR3Gw130_provenance.
- NP313448.RAUoZHpzeGMAU8-Tlv47DVVb-A0-EEtc9v4xD8jXXR3Gw130_assertion description "[Lafora disease (progressive myoclonus epilepsy of Lafora type) is an autosomal recessive neurodegenerative disorder resulting from defects in the EPM2A gene.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP313448.RAUoZHpzeGMAU8-Tlv47DVVb-A0-EEtc9v4xD8jXXR3Gw130_provenance.