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- source_evidence_literature type ECO_0000212 NP864423.RAYw2f7PtUZIFuwDLy0CRyADZjIbzn4py44PhptrTf2fg130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP864423.RAYw2f7PtUZIFuwDLy0CRyADZjIbzn4py44PhptrTf2fg130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP864423.RAYw2f7PtUZIFuwDLy0CRyADZjIbzn4py44PhptrTf2fg130_provenance.
- NP864423.RAYw2f7PtUZIFuwDLy0CRyADZjIbzn4py44PhptrTf2fg130_assertion description "[Autosomal-dominant centronuclear myopathy (CNM) due to mutations in the dynamin 2 gene (DNM2) is a rare congenital myopathy histopathologically characterized by centrally located nuclei and a radial arrangement of sarcoplasmic strands around the central nuclei.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP864423.RAYw2f7PtUZIFuwDLy0CRyADZjIbzn4py44PhptrTf2fg130_provenance.
- NP864423.RAYw2f7PtUZIFuwDLy0CRyADZjIbzn4py44PhptrTf2fg130_assertion evidence source_evidence_literature NP864423.RAYw2f7PtUZIFuwDLy0CRyADZjIbzn4py44PhptrTf2fg130_provenance.
- NP864423.RAYw2f7PtUZIFuwDLy0CRyADZjIbzn4py44PhptrTf2fg130_assertion SIO_000772 21221624 NP864423.RAYw2f7PtUZIFuwDLy0CRyADZjIbzn4py44PhptrTf2fg130_provenance.
- NP864423.RAYw2f7PtUZIFuwDLy0CRyADZjIbzn4py44PhptrTf2fg130_assertion wasDerivedFrom befree-2016 NP864423.RAYw2f7PtUZIFuwDLy0CRyADZjIbzn4py44PhptrTf2fg130_provenance.
- NP864423.RAYw2f7PtUZIFuwDLy0CRyADZjIbzn4py44PhptrTf2fg130_assertion wasGeneratedBy ECO_0000203 NP864423.RAYw2f7PtUZIFuwDLy0CRyADZjIbzn4py44PhptrTf2fg130_provenance.
- befree-2016 importedOn "2016-02-19" NP864423.RAYw2f7PtUZIFuwDLy0CRyADZjIbzn4py44PhptrTf2fg130_provenance.