Matches in Nanopublications for { <http://rdf.disgenet.org/nanopublications.trig#NP539600.RAqVa4HrvREvtN0UPy4SD7fm4zlyDCn4mTQdD4-oE6TwQ130_assertion> ?p ?o ?g. }
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- NP539600.RAqVa4HrvREvtN0UPy4SD7fm4zlyDCn4mTQdD4-oE6TwQ130_assertion type Assertion NP539600.RAqVa4HrvREvtN0UPy4SD7fm4zlyDCn4mTQdD4-oE6TwQ130_head.
- NP539600.RAqVa4HrvREvtN0UPy4SD7fm4zlyDCn4mTQdD4-oE6TwQ130_assertion description "[The conditions studied were scans of genetically confirmed cases of Becker muscular dystrophy (BMD) (n = 28), LGMD2C-F (sarcoglycanopathies) (n = 11), LGMD2I (n = 4), LGMD1B (n = 26), LGMD2A (n = 24), Bethlem myopathy (n = 14), and LGMD2L (n = 11).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP539600.RAqVa4HrvREvtN0UPy4SD7fm4zlyDCn4mTQdD4-oE6TwQ130_provenance.
- NP539600.RAqVa4HrvREvtN0UPy4SD7fm4zlyDCn4mTQdD4-oE6TwQ130_assertion evidence source_evidence_literature NP539600.RAqVa4HrvREvtN0UPy4SD7fm4zlyDCn4mTQdD4-oE6TwQ130_provenance.
- NP539600.RAqVa4HrvREvtN0UPy4SD7fm4zlyDCn4mTQdD4-oE6TwQ130_assertion SIO_000772 23035061 NP539600.RAqVa4HrvREvtN0UPy4SD7fm4zlyDCn4mTQdD4-oE6TwQ130_provenance.
- NP539600.RAqVa4HrvREvtN0UPy4SD7fm4zlyDCn4mTQdD4-oE6TwQ130_assertion wasDerivedFrom befree-20140225 NP539600.RAqVa4HrvREvtN0UPy4SD7fm4zlyDCn4mTQdD4-oE6TwQ130_provenance.
- NP539600.RAqVa4HrvREvtN0UPy4SD7fm4zlyDCn4mTQdD4-oE6TwQ130_assertion wasGeneratedBy ECO_0000203 NP539600.RAqVa4HrvREvtN0UPy4SD7fm4zlyDCn4mTQdD4-oE6TwQ130_provenance.