Matches in Nanopublications for { <http://rdf.disgenet.org/nanopublications.trig#NP590781.RACsJFhltcUKPN_Sv6vKEWypUd5LnmBJP7cgx98aMwItE130_assertion> ?p ?o ?g. }
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- NP590781.RACsJFhltcUKPN_Sv6vKEWypUd5LnmBJP7cgx98aMwItE130_assertion type Assertion NP590781.RACsJFhltcUKPN_Sv6vKEWypUd5LnmBJP7cgx98aMwItE130_head.
- NP590781.RACsJFhltcUKPN_Sv6vKEWypUd5LnmBJP7cgx98aMwItE130_assertion description "[X-linked hydrocephalus, MASA syndrome and certain forms of X-linked spastic paraplegia and agenesis of corpus callosum are now known to be due to mutations in the gene for the neural cell adhesion molecule L1 (19, 30).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP590781.RACsJFhltcUKPN_Sv6vKEWypUd5LnmBJP7cgx98aMwItE130_provenance.
- NP590781.RACsJFhltcUKPN_Sv6vKEWypUd5LnmBJP7cgx98aMwItE130_assertion evidence source_evidence_literature NP590781.RACsJFhltcUKPN_Sv6vKEWypUd5LnmBJP7cgx98aMwItE130_provenance.
- NP590781.RACsJFhltcUKPN_Sv6vKEWypUd5LnmBJP7cgx98aMwItE130_assertion SIO_000772 9266556 NP590781.RACsJFhltcUKPN_Sv6vKEWypUd5LnmBJP7cgx98aMwItE130_provenance.
- NP590781.RACsJFhltcUKPN_Sv6vKEWypUd5LnmBJP7cgx98aMwItE130_assertion wasDerivedFrom befree-20140225 NP590781.RACsJFhltcUKPN_Sv6vKEWypUd5LnmBJP7cgx98aMwItE130_provenance.
- NP590781.RACsJFhltcUKPN_Sv6vKEWypUd5LnmBJP7cgx98aMwItE130_assertion wasGeneratedBy ECO_0000203 NP590781.RACsJFhltcUKPN_Sv6vKEWypUd5LnmBJP7cgx98aMwItE130_provenance.