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- source_evidence_literature type ECO_0000212 NP1158069.RAJzGEMYlkjwIh6mxlLOaJaCNldumn0-GmeLfAN5GjUnQ130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP1158069.RAJzGEMYlkjwIh6mxlLOaJaCNldumn0-GmeLfAN5GjUnQ130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP1158069.RAJzGEMYlkjwIh6mxlLOaJaCNldumn0-GmeLfAN5GjUnQ130_provenance.
- NP1158069.RAJzGEMYlkjwIh6mxlLOaJaCNldumn0-GmeLfAN5GjUnQ130_assertion description "[The most severe form of the disease, X-linked centronuclear myopathy, is due to mutations in the gene encoding myotubularin (MTM1), while mutations in dynamin 2 (DNM2) and amphiphysin 2/BIN1 (AMPH2) cause milder forms of myopathy.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1158069.RAJzGEMYlkjwIh6mxlLOaJaCNldumn0-GmeLfAN5GjUnQ130_provenance.
- NP1158069.RAJzGEMYlkjwIh6mxlLOaJaCNldumn0-GmeLfAN5GjUnQ130_assertion evidence source_evidence_literature NP1158069.RAJzGEMYlkjwIh6mxlLOaJaCNldumn0-GmeLfAN5GjUnQ130_provenance.
- NP1158069.RAJzGEMYlkjwIh6mxlLOaJaCNldumn0-GmeLfAN5GjUnQ130_assertion SIO_000772 24569368 NP1158069.RAJzGEMYlkjwIh6mxlLOaJaCNldumn0-GmeLfAN5GjUnQ130_provenance.
- NP1158069.RAJzGEMYlkjwIh6mxlLOaJaCNldumn0-GmeLfAN5GjUnQ130_assertion wasDerivedFrom befree-2016 NP1158069.RAJzGEMYlkjwIh6mxlLOaJaCNldumn0-GmeLfAN5GjUnQ130_provenance.
- NP1158069.RAJzGEMYlkjwIh6mxlLOaJaCNldumn0-GmeLfAN5GjUnQ130_assertion wasGeneratedBy ECO_0000203 NP1158069.RAJzGEMYlkjwIh6mxlLOaJaCNldumn0-GmeLfAN5GjUnQ130_provenance.
- befree-2016 importedOn "2016-02-19" NP1158069.RAJzGEMYlkjwIh6mxlLOaJaCNldumn0-GmeLfAN5GjUnQ130_provenance.