Matches in Nanopublications for { <http://rdf.disgenet.org/nanopublications.trig#NP688347.RA4Hzj6iLfb9pPjW9ReWBAn7McO1Rpv1Iw6upadI0MnjQ130_assertion> ?p ?o ?g. }
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- NP688347.RA4Hzj6iLfb9pPjW9ReWBAn7McO1Rpv1Iw6upadI0MnjQ130_assertion type Assertion NP688347.RA4Hzj6iLfb9pPjW9ReWBAn7McO1Rpv1Iw6upadI0MnjQ130_head.
- NP688347.RA4Hzj6iLfb9pPjW9ReWBAn7McO1Rpv1Iw6upadI0MnjQ130_assertion description "[PROMM (proximal myotonic myopathy) and DM2 (myotonic dystrophy Type 2) are autosomal dominant multisystem disorders that have both been linked to chromosome 3q.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP688347.RA4Hzj6iLfb9pPjW9ReWBAn7McO1Rpv1Iw6upadI0MnjQ130_provenance.
- NP688347.RA4Hzj6iLfb9pPjW9ReWBAn7McO1Rpv1Iw6upadI0MnjQ130_assertion evidence source_evidence_literature NP688347.RA4Hzj6iLfb9pPjW9ReWBAn7McO1Rpv1Iw6upadI0MnjQ130_provenance.
- NP688347.RA4Hzj6iLfb9pPjW9ReWBAn7McO1Rpv1Iw6upadI0MnjQ130_assertion SIO_000772 15261229 NP688347.RA4Hzj6iLfb9pPjW9ReWBAn7McO1Rpv1Iw6upadI0MnjQ130_provenance.
- NP688347.RA4Hzj6iLfb9pPjW9ReWBAn7McO1Rpv1Iw6upadI0MnjQ130_assertion wasDerivedFrom befree-20140225 NP688347.RA4Hzj6iLfb9pPjW9ReWBAn7McO1Rpv1Iw6upadI0MnjQ130_provenance.
- NP688347.RA4Hzj6iLfb9pPjW9ReWBAn7McO1Rpv1Iw6upadI0MnjQ130_assertion wasGeneratedBy ECO_0000203 NP688347.RA4Hzj6iLfb9pPjW9ReWBAn7McO1Rpv1Iw6upadI0MnjQ130_provenance.