Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP782568.RAlotvGxVO00bfe5YDCIAS_rLyVoWDZUaemRZbb5RDAgw130_assertion> ?p ?o ?g. }
Showing items 1 to 6 of
6
with 100 items per page.
- NP782568.RAlotvGxVO00bfe5YDCIAS_rLyVoWDZUaemRZbb5RDAgw130_assertion type Assertion NP782568.RAlotvGxVO00bfe5YDCIAS_rLyVoWDZUaemRZbb5RDAgw130_head.
- NP782568.RAlotvGxVO00bfe5YDCIAS_rLyVoWDZUaemRZbb5RDAgw130_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." NP782568.RAlotvGxVO00bfe5YDCIAS_rLyVoWDZUaemRZbb5RDAgw130_provenance.
- NP782568.RAlotvGxVO00bfe5YDCIAS_rLyVoWDZUaemRZbb5RDAgw130_assertion evidence source_evidence_literature NP782568.RAlotvGxVO00bfe5YDCIAS_rLyVoWDZUaemRZbb5RDAgw130_provenance.
- NP782568.RAlotvGxVO00bfe5YDCIAS_rLyVoWDZUaemRZbb5RDAgw130_assertion SIO_000772 15596616 NP782568.RAlotvGxVO00bfe5YDCIAS_rLyVoWDZUaemRZbb5RDAgw130_provenance.
- NP782568.RAlotvGxVO00bfe5YDCIAS_rLyVoWDZUaemRZbb5RDAgw130_assertion wasDerivedFrom befree-20150227 NP782568.RAlotvGxVO00bfe5YDCIAS_rLyVoWDZUaemRZbb5RDAgw130_provenance.
- NP782568.RAlotvGxVO00bfe5YDCIAS_rLyVoWDZUaemRZbb5RDAgw130_assertion wasGeneratedBy ECO_0000203 NP782568.RAlotvGxVO00bfe5YDCIAS_rLyVoWDZUaemRZbb5RDAgw130_provenance.