Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP824754.RArID63kYQh-pv2uYVQeqGxd5NNOwJeeSKZoVIsehQ1NY130_assertion> ?p ?o ?g. }
Showing items 1 to 6 of
6
with 100 items per page.
- NP824754.RArID63kYQh-pv2uYVQeqGxd5NNOwJeeSKZoVIsehQ1NY130_assertion type Assertion NP824754.RArID63kYQh-pv2uYVQeqGxd5NNOwJeeSKZoVIsehQ1NY130_head.
- NP824754.RArID63kYQh-pv2uYVQeqGxd5NNOwJeeSKZoVIsehQ1NY130_assertion wasGeneratedBy ECO_0000203 NP824754.RArID63kYQh-pv2uYVQeqGxd5NNOwJeeSKZoVIsehQ1NY130_provenance.
- NP824754.RArID63kYQh-pv2uYVQeqGxd5NNOwJeeSKZoVIsehQ1NY130_assertion wasDerivedFrom befree-20150227 NP824754.RArID63kYQh-pv2uYVQeqGxd5NNOwJeeSKZoVIsehQ1NY130_provenance.
- NP824754.RArID63kYQh-pv2uYVQeqGxd5NNOwJeeSKZoVIsehQ1NY130_assertion SIO_000772 21336781 NP824754.RArID63kYQh-pv2uYVQeqGxd5NNOwJeeSKZoVIsehQ1NY130_provenance.
- NP824754.RArID63kYQh-pv2uYVQeqGxd5NNOwJeeSKZoVIsehQ1NY130_assertion evidence source_evidence_literature NP824754.RArID63kYQh-pv2uYVQeqGxd5NNOwJeeSKZoVIsehQ1NY130_provenance.
- NP824754.RArID63kYQh-pv2uYVQeqGxd5NNOwJeeSKZoVIsehQ1NY130_assertion description "[Here we describe a patient with limb girdle muscular dystrophy 1A (LGMD1A) due to a novel myotilin gene (MYOT) mutation with late onset, rapid progression, loss of ambulation and respiratory failure.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP824754.RArID63kYQh-pv2uYVQeqGxd5NNOwJeeSKZoVIsehQ1NY130_provenance.