Matches in Nanopublications for { <http://rdf.disgenet.org/nanopublications.trig#NP156088.RArf6g0vAgyr6wIv0pNFYEjTcoFumVS7Xb--iA67de4vY130_assertion> ?p ?o ?g. }
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- NP156088.RArf6g0vAgyr6wIv0pNFYEjTcoFumVS7Xb--iA67de4vY130_assertion type Assertion NP156088.RArf6g0vAgyr6wIv0pNFYEjTcoFumVS7Xb--iA67de4vY130_head.
- NP156088.RArf6g0vAgyr6wIv0pNFYEjTcoFumVS7Xb--iA67de4vY130_assertion description "[Hence, these studies identify novel biological functions for merosin in myoblast fusion and muscle cell survival; furthermore, these explain some of the pathogenic events observed in congenital muscular dystrophy caused by merosin deficiency and provide in vitro models to further investigate the molecular mechanisms of this disease.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP156088.RArf6g0vAgyr6wIv0pNFYEjTcoFumVS7Xb--iA67de4vY130_provenance.
- NP156088.RArf6g0vAgyr6wIv0pNFYEjTcoFumVS7Xb--iA67de4vY130_assertion evidence source_evidence_literature NP156088.RArf6g0vAgyr6wIv0pNFYEjTcoFumVS7Xb--iA67de4vY130_provenance.
- NP156088.RArf6g0vAgyr6wIv0pNFYEjTcoFumVS7Xb--iA67de4vY130_assertion SIO_000772 8830776 NP156088.RArf6g0vAgyr6wIv0pNFYEjTcoFumVS7Xb--iA67de4vY130_provenance.
- NP156088.RArf6g0vAgyr6wIv0pNFYEjTcoFumVS7Xb--iA67de4vY130_assertion wasDerivedFrom befree-20140225 NP156088.RArf6g0vAgyr6wIv0pNFYEjTcoFumVS7Xb--iA67de4vY130_provenance.
- NP156088.RArf6g0vAgyr6wIv0pNFYEjTcoFumVS7Xb--iA67de4vY130_assertion wasGeneratedBy ECO_0000203 NP156088.RArf6g0vAgyr6wIv0pNFYEjTcoFumVS7Xb--iA67de4vY130_provenance.