Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP226778.RAilH4NrWA2Ua3gEcWBHif_zzl9XUWTSu_28Bjdi72GRU130_assertion> ?p ?o ?g. }
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- NP226778.RAilH4NrWA2Ua3gEcWBHif_zzl9XUWTSu_28Bjdi72GRU130_assertion type Assertion NP226778.RAilH4NrWA2Ua3gEcWBHif_zzl9XUWTSu_28Bjdi72GRU130_head.
- NP226778.RAilH4NrWA2Ua3gEcWBHif_zzl9XUWTSu_28Bjdi72GRU130_assertion description "[Malignant mutation in lamin A/C gene causing progressive conduction system disease and early death in limb-girdle muscular dystrophy.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP226778.RAilH4NrWA2Ua3gEcWBHif_zzl9XUWTSu_28Bjdi72GRU130_provenance.
- NP226778.RAilH4NrWA2Ua3gEcWBHif_zzl9XUWTSu_28Bjdi72GRU130_assertion evidence source_evidence_literature NP226778.RAilH4NrWA2Ua3gEcWBHif_zzl9XUWTSu_28Bjdi72GRU130_provenance.
- NP226778.RAilH4NrWA2Ua3gEcWBHif_zzl9XUWTSu_28Bjdi72GRU130_assertion SIO_000772 17605093 NP226778.RAilH4NrWA2Ua3gEcWBHif_zzl9XUWTSu_28Bjdi72GRU130_provenance.
- NP226778.RAilH4NrWA2Ua3gEcWBHif_zzl9XUWTSu_28Bjdi72GRU130_assertion wasDerivedFrom lhgdn-20090331 NP226778.RAilH4NrWA2Ua3gEcWBHif_zzl9XUWTSu_28Bjdi72GRU130_provenance.
- NP226778.RAilH4NrWA2Ua3gEcWBHif_zzl9XUWTSu_28Bjdi72GRU130_assertion wasGeneratedBy ECO_0000203 NP226778.RAilH4NrWA2Ua3gEcWBHif_zzl9XUWTSu_28Bjdi72GRU130_provenance.