Matches in Nanopublications for { <http://rdf.disgenet.org/nanopublications.trig#NP698478.RAgwhs0CouNUUexbN96ANt7S9nxWcaAG9GSsvaQYHemt4130_assertion> ?p ?o ?g. }
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- NP698478.RAgwhs0CouNUUexbN96ANt7S9nxWcaAG9GSsvaQYHemt4130_assertion type Assertion NP698478.RAgwhs0CouNUUexbN96ANt7S9nxWcaAG9GSsvaQYHemt4130_head.
- NP698478.RAgwhs0CouNUUexbN96ANt7S9nxWcaAG9GSsvaQYHemt4130_assertion wasGeneratedBy ECO_0000203 NP698478.RAgwhs0CouNUUexbN96ANt7S9nxWcaAG9GSsvaQYHemt4130_provenance.
- NP698478.RAgwhs0CouNUUexbN96ANt7S9nxWcaAG9GSsvaQYHemt4130_assertion wasDerivedFrom befree-20140225 NP698478.RAgwhs0CouNUUexbN96ANt7S9nxWcaAG9GSsvaQYHemt4130_provenance.
- NP698478.RAgwhs0CouNUUexbN96ANt7S9nxWcaAG9GSsvaQYHemt4130_assertion SIO_000772 22407275 NP698478.RAgwhs0CouNUUexbN96ANt7S9nxWcaAG9GSsvaQYHemt4130_provenance.
- NP698478.RAgwhs0CouNUUexbN96ANt7S9nxWcaAG9GSsvaQYHemt4130_assertion evidence source_evidence_literature NP698478.RAgwhs0CouNUUexbN96ANt7S9nxWcaAG9GSsvaQYHemt4130_provenance.
- NP698478.RAgwhs0CouNUUexbN96ANt7S9nxWcaAG9GSsvaQYHemt4130_assertion description "[Myotonic dystrophy type 2 (DM2) is a common adult onset muscular dystrophy caused by a dominantly transmitted (CCTG)( n ) expansion in intron 1 of the CNBP gene.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP698478.RAgwhs0CouNUUexbN96ANt7S9nxWcaAG9GSsvaQYHemt4130_provenance.