Matches in Nanopublications for { <http://rdf.disgenet.org/nanopublications.trig#NP461552.RA6Gg-gpFOG6S1KXI6L365G6IpuodR4ZUXSfpO8QmFDAQ130_assertion> ?p ?o ?g. }
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- NP461552.RA6Gg-gpFOG6S1KXI6L365G6IpuodR4ZUXSfpO8QmFDAQ130_assertion type Assertion NP461552.RA6Gg-gpFOG6S1KXI6L365G6IpuodR4ZUXSfpO8QmFDAQ130_head.
- NP461552.RA6Gg-gpFOG6S1KXI6L365G6IpuodR4ZUXSfpO8QmFDAQ130_assertion description "[Myotonic dystrophy type 2/proximal myotonic myopathy (DM2/PROMM) is an autosomal dominant multisystem disorder.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP461552.RA6Gg-gpFOG6S1KXI6L365G6IpuodR4ZUXSfpO8QmFDAQ130_provenance.
- NP461552.RA6Gg-gpFOG6S1KXI6L365G6IpuodR4ZUXSfpO8QmFDAQ130_assertion evidence source_evidence_literature NP461552.RA6Gg-gpFOG6S1KXI6L365G6IpuodR4ZUXSfpO8QmFDAQ130_provenance.
- NP461552.RA6Gg-gpFOG6S1KXI6L365G6IpuodR4ZUXSfpO8QmFDAQ130_assertion SIO_000772 15596616 NP461552.RA6Gg-gpFOG6S1KXI6L365G6IpuodR4ZUXSfpO8QmFDAQ130_provenance.
- NP461552.RA6Gg-gpFOG6S1KXI6L365G6IpuodR4ZUXSfpO8QmFDAQ130_assertion wasDerivedFrom befree-20140225 NP461552.RA6Gg-gpFOG6S1KXI6L365G6IpuodR4ZUXSfpO8QmFDAQ130_provenance.
- NP461552.RA6Gg-gpFOG6S1KXI6L365G6IpuodR4ZUXSfpO8QmFDAQ130_assertion wasGeneratedBy ECO_0000203 NP461552.RA6Gg-gpFOG6S1KXI6L365G6IpuodR4ZUXSfpO8QmFDAQ130_provenance.