Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP782590.RAXc5MJgoFeMFwgI2gHy7FlCpD5omdT6aiStFv-8XRoeQ130_assertion> ?p ?o ?g. }
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- NP782590.RAXc5MJgoFeMFwgI2gHy7FlCpD5omdT6aiStFv-8XRoeQ130_assertion type Assertion NP782590.RAXc5MJgoFeMFwgI2gHy7FlCpD5omdT6aiStFv-8XRoeQ130_head.
- NP782590.RAXc5MJgoFeMFwgI2gHy7FlCpD5omdT6aiStFv-8XRoeQ130_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." NP782590.RAXc5MJgoFeMFwgI2gHy7FlCpD5omdT6aiStFv-8XRoeQ130_provenance.
- NP782590.RAXc5MJgoFeMFwgI2gHy7FlCpD5omdT6aiStFv-8XRoeQ130_assertion evidence source_evidence_literature NP782590.RAXc5MJgoFeMFwgI2gHy7FlCpD5omdT6aiStFv-8XRoeQ130_provenance.
- NP782590.RAXc5MJgoFeMFwgI2gHy7FlCpD5omdT6aiStFv-8XRoeQ130_assertion SIO_000772 15596616 NP782590.RAXc5MJgoFeMFwgI2gHy7FlCpD5omdT6aiStFv-8XRoeQ130_provenance.
- NP782590.RAXc5MJgoFeMFwgI2gHy7FlCpD5omdT6aiStFv-8XRoeQ130_assertion wasDerivedFrom befree-20150227 NP782590.RAXc5MJgoFeMFwgI2gHy7FlCpD5omdT6aiStFv-8XRoeQ130_provenance.
- NP782590.RAXc5MJgoFeMFwgI2gHy7FlCpD5omdT6aiStFv-8XRoeQ130_assertion wasGeneratedBy ECO_0000203 NP782590.RAXc5MJgoFeMFwgI2gHy7FlCpD5omdT6aiStFv-8XRoeQ130_provenance.