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- NP530334.RATi2B2ml-W24L963fQHrOG2jD_hVCIs-kM5_zZZaWCFo130_assertion type Assertion NP530334.RATi2B2ml-W24L963fQHrOG2jD_hVCIs-kM5_zZZaWCFo130_head.
- NP530334.RATi2B2ml-W24L963fQHrOG2jD_hVCIs-kM5_zZZaWCFo130_assertion wasGeneratedBy ECO_0000203 NP530334.RATi2B2ml-W24L963fQHrOG2jD_hVCIs-kM5_zZZaWCFo130_provenance.
- NP530334.RATi2B2ml-W24L963fQHrOG2jD_hVCIs-kM5_zZZaWCFo130_assertion wasDerivedFrom befree-20150227 NP530334.RATi2B2ml-W24L963fQHrOG2jD_hVCIs-kM5_zZZaWCFo130_provenance.
- NP530334.RATi2B2ml-W24L963fQHrOG2jD_hVCIs-kM5_zZZaWCFo130_assertion SIO_000772 9027848 NP530334.RATi2B2ml-W24L963fQHrOG2jD_hVCIs-kM5_zZZaWCFo130_provenance.
- NP530334.RATi2B2ml-W24L963fQHrOG2jD_hVCIs-kM5_zZZaWCFo130_assertion evidence source_evidence_literature NP530334.RATi2B2ml-W24L963fQHrOG2jD_hVCIs-kM5_zZZaWCFo130_provenance.
- NP530334.RATi2B2ml-W24L963fQHrOG2jD_hVCIs-kM5_zZZaWCFo130_assertion description "[Merosin-deficient congenital muscular dystrophy (CMD) is caused by mutations in the laminin alpha 2 chain gene.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP530334.RATi2B2ml-W24L963fQHrOG2jD_hVCIs-kM5_zZZaWCFo130_provenance.