Matches in Nanopublications for { <http://rdf.disgenet.org/nanopublications.trig#NP195652.RABcbomPVLE1TTBPj5I2peXe7fV88fMVJKZp7rj2WcE5U130_assertion> ?p ?o ?g. }
Showing items 1 to 6 of
6
with 100 items per page.
- NP195652.RABcbomPVLE1TTBPj5I2peXe7fV88fMVJKZp7rj2WcE5U130_assertion type Assertion NP195652.RABcbomPVLE1TTBPj5I2peXe7fV88fMVJKZp7rj2WcE5U130_head.
- NP195652.RABcbomPVLE1TTBPj5I2peXe7fV88fMVJKZp7rj2WcE5U130_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." NP195652.RABcbomPVLE1TTBPj5I2peXe7fV88fMVJKZp7rj2WcE5U130_provenance.
- NP195652.RABcbomPVLE1TTBPj5I2peXe7fV88fMVJKZp7rj2WcE5U130_assertion evidence source_evidence_literature NP195652.RABcbomPVLE1TTBPj5I2peXe7fV88fMVJKZp7rj2WcE5U130_provenance.
- NP195652.RABcbomPVLE1TTBPj5I2peXe7fV88fMVJKZp7rj2WcE5U130_assertion SIO_000772 15596616 NP195652.RABcbomPVLE1TTBPj5I2peXe7fV88fMVJKZp7rj2WcE5U130_provenance.
- NP195652.RABcbomPVLE1TTBPj5I2peXe7fV88fMVJKZp7rj2WcE5U130_assertion wasDerivedFrom befree-20140225 NP195652.RABcbomPVLE1TTBPj5I2peXe7fV88fMVJKZp7rj2WcE5U130_provenance.
- NP195652.RABcbomPVLE1TTBPj5I2peXe7fV88fMVJKZp7rj2WcE5U130_assertion wasGeneratedBy ECO_0000203 NP195652.RABcbomPVLE1TTBPj5I2peXe7fV88fMVJKZp7rj2WcE5U130_provenance.