Matches in Nanopublications for { <http://rdf.disgenet.org/nanopublications.trig#NP285472.RAdm3IEioPV8f1rBqIL9SLWgG_meJcu2FMUAkH3_DxXuY130_assertion> ?p ?o ?g. }
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- NP285472.RAdm3IEioPV8f1rBqIL9SLWgG_meJcu2FMUAkH3_DxXuY130_assertion type Assertion NP285472.RAdm3IEioPV8f1rBqIL9SLWgG_meJcu2FMUAkH3_DxXuY130_head.
- NP285472.RAdm3IEioPV8f1rBqIL9SLWgG_meJcu2FMUAkH3_DxXuY130_assertion description "[A founder mutation in BBS2 is responsible for Bardet-Biedl syndrome in the Hutterite population: utility of SNP arrays in genetically heterogeneous disorders.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP285472.RAdm3IEioPV8f1rBqIL9SLWgG_meJcu2FMUAkH3_DxXuY130_provenance.
- NP285472.RAdm3IEioPV8f1rBqIL9SLWgG_meJcu2FMUAkH3_DxXuY130_assertion evidence source_evidence_literature NP285472.RAdm3IEioPV8f1rBqIL9SLWgG_meJcu2FMUAkH3_DxXuY130_provenance.
- NP285472.RAdm3IEioPV8f1rBqIL9SLWgG_meJcu2FMUAkH3_DxXuY130_assertion SIO_000772 20618352 NP285472.RAdm3IEioPV8f1rBqIL9SLWgG_meJcu2FMUAkH3_DxXuY130_provenance.
- NP285472.RAdm3IEioPV8f1rBqIL9SLWgG_meJcu2FMUAkH3_DxXuY130_assertion wasDerivedFrom befree-20140225 NP285472.RAdm3IEioPV8f1rBqIL9SLWgG_meJcu2FMUAkH3_DxXuY130_provenance.
- NP285472.RAdm3IEioPV8f1rBqIL9SLWgG_meJcu2FMUAkH3_DxXuY130_assertion wasGeneratedBy ECO_0000203 NP285472.RAdm3IEioPV8f1rBqIL9SLWgG_meJcu2FMUAkH3_DxXuY130_provenance.