Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP777254.RAo4CIwSH7PeEPJL19qSWEWK_zC9OQ2SiRf1c8sX10xAg130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP777254.RAo4CIwSH7PeEPJL19qSWEWK_zC9OQ2SiRf1c8sX10xAg130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP777254.RAo4CIwSH7PeEPJL19qSWEWK_zC9OQ2SiRf1c8sX10xAg130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP777254.RAo4CIwSH7PeEPJL19qSWEWK_zC9OQ2SiRf1c8sX10xAg130_provenance.
- NP777254.RAo4CIwSH7PeEPJL19qSWEWK_zC9OQ2SiRf1c8sX10xAg130_assertion description "[Whilst DNM2-related CMT may feature non-neurological findings including cataracts, this has not been reported in DNM2-related centronuclear myopathy.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP777254.RAo4CIwSH7PeEPJL19qSWEWK_zC9OQ2SiRf1c8sX10xAg130_provenance.
- NP777254.RAo4CIwSH7PeEPJL19qSWEWK_zC9OQ2SiRf1c8sX10xAg130_assertion evidence source_evidence_literature NP777254.RAo4CIwSH7PeEPJL19qSWEWK_zC9OQ2SiRf1c8sX10xAg130_provenance.
- NP777254.RAo4CIwSH7PeEPJL19qSWEWK_zC9OQ2SiRf1c8sX10xAg130_assertion SIO_000772 19932620 NP777254.RAo4CIwSH7PeEPJL19qSWEWK_zC9OQ2SiRf1c8sX10xAg130_provenance.
- NP777254.RAo4CIwSH7PeEPJL19qSWEWK_zC9OQ2SiRf1c8sX10xAg130_assertion wasDerivedFrom befree-2016 NP777254.RAo4CIwSH7PeEPJL19qSWEWK_zC9OQ2SiRf1c8sX10xAg130_provenance.
- NP777254.RAo4CIwSH7PeEPJL19qSWEWK_zC9OQ2SiRf1c8sX10xAg130_assertion wasGeneratedBy ECO_0000203 NP777254.RAo4CIwSH7PeEPJL19qSWEWK_zC9OQ2SiRf1c8sX10xAg130_provenance.
- befree-2016 importedOn "2016-02-19" NP777254.RAo4CIwSH7PeEPJL19qSWEWK_zC9OQ2SiRf1c8sX10xAg130_provenance.