Matches in Nanopublications for { <http://rdf.disgenet.org/nanopublications.trig#NP416579.RAy-S-UPuvJrRFvYRHEW24cpf16HB5sV-FCOE_sgRkBWQ130_assertion> ?p ?o ?g. }
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- NP416579.RAy-S-UPuvJrRFvYRHEW24cpf16HB5sV-FCOE_sgRkBWQ130_assertion type Assertion NP416579.RAy-S-UPuvJrRFvYRHEW24cpf16HB5sV-FCOE_sgRkBWQ130_head.
- NP416579.RAy-S-UPuvJrRFvYRHEW24cpf16HB5sV-FCOE_sgRkBWQ130_assertion wasGeneratedBy ECO_0000203 NP416579.RAy-S-UPuvJrRFvYRHEW24cpf16HB5sV-FCOE_sgRkBWQ130_provenance.
- NP416579.RAy-S-UPuvJrRFvYRHEW24cpf16HB5sV-FCOE_sgRkBWQ130_assertion wasDerivedFrom befree-20140225 NP416579.RAy-S-UPuvJrRFvYRHEW24cpf16HB5sV-FCOE_sgRkBWQ130_provenance.
- NP416579.RAy-S-UPuvJrRFvYRHEW24cpf16HB5sV-FCOE_sgRkBWQ130_assertion SIO_000772 12467726 NP416579.RAy-S-UPuvJrRFvYRHEW24cpf16HB5sV-FCOE_sgRkBWQ130_provenance.
- NP416579.RAy-S-UPuvJrRFvYRHEW24cpf16HB5sV-FCOE_sgRkBWQ130_assertion evidence source_evidence_literature NP416579.RAy-S-UPuvJrRFvYRHEW24cpf16HB5sV-FCOE_sgRkBWQ130_provenance.
- NP416579.RAy-S-UPuvJrRFvYRHEW24cpf16HB5sV-FCOE_sgRkBWQ130_assertion description "[Merosin-deficient congenital muscular dystrophy with mental retardation and cerebellar cysts, unlinked to the LAMA2, FCMD, MEB and CMD1B loci, in three Tunisian patients.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP416579.RAy-S-UPuvJrRFvYRHEW24cpf16HB5sV-FCOE_sgRkBWQ130_provenance.