Matches in Nanopublications for { <http://rdf.disgenet.org/nanopublications.trig#NP455026.RAG5uzfx6bXABPTcKPih5HmLZp4wgcCt_Fz6JFQP7-zSw130_assertion> ?p ?o ?g. }
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- NP455026.RAG5uzfx6bXABPTcKPih5HmLZp4wgcCt_Fz6JFQP7-zSw130_assertion type Assertion NP455026.RAG5uzfx6bXABPTcKPih5HmLZp4wgcCt_Fz6JFQP7-zSw130_head.
- NP455026.RAG5uzfx6bXABPTcKPih5HmLZp4wgcCt_Fz6JFQP7-zSw130_assertion description "[All patients with POMT1 and POMT2 mutations had evidence of either structural or functional central nervous system involvement including four patients with mental retardation and a LGMD phenotype.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP455026.RAG5uzfx6bXABPTcKPih5HmLZp4wgcCt_Fz6JFQP7-zSw130_provenance.
- NP455026.RAG5uzfx6bXABPTcKPih5HmLZp4wgcCt_Fz6JFQP7-zSw130_assertion evidence source_evidence_literature NP455026.RAG5uzfx6bXABPTcKPih5HmLZp4wgcCt_Fz6JFQP7-zSw130_provenance.
- NP455026.RAG5uzfx6bXABPTcKPih5HmLZp4wgcCt_Fz6JFQP7-zSw130_assertion SIO_000772 17878207 NP455026.RAG5uzfx6bXABPTcKPih5HmLZp4wgcCt_Fz6JFQP7-zSw130_provenance.
- NP455026.RAG5uzfx6bXABPTcKPih5HmLZp4wgcCt_Fz6JFQP7-zSw130_assertion wasDerivedFrom befree-20140225 NP455026.RAG5uzfx6bXABPTcKPih5HmLZp4wgcCt_Fz6JFQP7-zSw130_provenance.
- NP455026.RAG5uzfx6bXABPTcKPih5HmLZp4wgcCt_Fz6JFQP7-zSw130_assertion wasGeneratedBy ECO_0000203 NP455026.RAG5uzfx6bXABPTcKPih5HmLZp4wgcCt_Fz6JFQP7-zSw130_provenance.