Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP919531.RAyul4rK1k2uOs-U6HdvSpDKfCXZj_0Cpj0ZL2gv98Y0M130_assertion> ?p ?o ?g. }
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- NP919531.RAyul4rK1k2uOs-U6HdvSpDKfCXZj_0Cpj0ZL2gv98Y0M130_assertion type Assertion NP919531.RAyul4rK1k2uOs-U6HdvSpDKfCXZj_0Cpj0ZL2gv98Y0M130_head.
- NP919531.RAyul4rK1k2uOs-U6HdvSpDKfCXZj_0Cpj0ZL2gv98Y0M130_assertion description "[The secondary ?-dystroglycanopathies usually present in infancy as congenital muscular dystrophies but may manifest later in childhood or adult life (limb-girdle muscular dystrophy (LGMD) 2I, LGMD2K, LGMD2M, LGMD2N, and LGMD2O).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP919531.RAyul4rK1k2uOs-U6HdvSpDKfCXZj_0Cpj0ZL2gv98Y0M130_provenance.
- NP919531.RAyul4rK1k2uOs-U6HdvSpDKfCXZj_0Cpj0ZL2gv98Y0M130_assertion evidence source_evidence_literature NP919531.RAyul4rK1k2uOs-U6HdvSpDKfCXZj_0Cpj0ZL2gv98Y0M130_provenance.
- NP919531.RAyul4rK1k2uOs-U6HdvSpDKfCXZj_0Cpj0ZL2gv98Y0M130_assertion SIO_000772 21496628 NP919531.RAyul4rK1k2uOs-U6HdvSpDKfCXZj_0Cpj0ZL2gv98Y0M130_provenance.
- NP919531.RAyul4rK1k2uOs-U6HdvSpDKfCXZj_0Cpj0ZL2gv98Y0M130_assertion wasDerivedFrom befree-20150227 NP919531.RAyul4rK1k2uOs-U6HdvSpDKfCXZj_0Cpj0ZL2gv98Y0M130_provenance.
- NP919531.RAyul4rK1k2uOs-U6HdvSpDKfCXZj_0Cpj0ZL2gv98Y0M130_assertion wasGeneratedBy ECO_0000203 NP919531.RAyul4rK1k2uOs-U6HdvSpDKfCXZj_0Cpj0ZL2gv98Y0M130_provenance.