Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP333851.RAC9LauUsnbg7B0azTR8IKgTOtxvRAI1g9sVwS6yd5p4o130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP333851.RAC9LauUsnbg7B0azTR8IKgTOtxvRAI1g9sVwS6yd5p4o130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP333851.RAC9LauUsnbg7B0azTR8IKgTOtxvRAI1g9sVwS6yd5p4o130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP333851.RAC9LauUsnbg7B0azTR8IKgTOtxvRAI1g9sVwS6yd5p4o130_provenance.
- NP333851.RAC9LauUsnbg7B0azTR8IKgTOtxvRAI1g9sVwS6yd5p4o130_assertion description "[Unverricht-Lundborg disease (ULD), progressive myoclonic epilepsy type 1 (EPM1, OMIM254800), is an autosomal recessively inherited neurodegenerative disorder characterized by age of onset from 6 to 16 years, stimulus-sensitive myoclonus, and tonic-clonic epileptic seizures.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP333851.RAC9LauUsnbg7B0azTR8IKgTOtxvRAI1g9sVwS6yd5p4o130_provenance.
- NP333851.RAC9LauUsnbg7B0azTR8IKgTOtxvRAI1g9sVwS6yd5p4o130_assertion evidence source_evidence_literature NP333851.RAC9LauUsnbg7B0azTR8IKgTOtxvRAI1g9sVwS6yd5p4o130_provenance.
- NP333851.RAC9LauUsnbg7B0azTR8IKgTOtxvRAI1g9sVwS6yd5p4o130_assertion SIO_000772 18325013 NP333851.RAC9LauUsnbg7B0azTR8IKgTOtxvRAI1g9sVwS6yd5p4o130_provenance.
- NP333851.RAC9LauUsnbg7B0azTR8IKgTOtxvRAI1g9sVwS6yd5p4o130_assertion wasDerivedFrom befree-20150227 NP333851.RAC9LauUsnbg7B0azTR8IKgTOtxvRAI1g9sVwS6yd5p4o130_provenance.
- NP333851.RAC9LauUsnbg7B0azTR8IKgTOtxvRAI1g9sVwS6yd5p4o130_assertion wasGeneratedBy ECO_0000203 NP333851.RAC9LauUsnbg7B0azTR8IKgTOtxvRAI1g9sVwS6yd5p4o130_provenance.
- befree-20150227 importedOn "2015-02-27" NP333851.RAC9LauUsnbg7B0azTR8IKgTOtxvRAI1g9sVwS6yd5p4o130_provenance.