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- NP315833.RA8K0h4u1rCqKp2jl3XoU8N2evyLplzkxDZaDXtJBJB5s130_assertion type Assertion NP315833.RA8K0h4u1rCqKp2jl3XoU8N2evyLplzkxDZaDXtJBJB5s130_head.
- NP315833.RA8K0h4u1rCqKp2jl3XoU8N2evyLplzkxDZaDXtJBJB5s130_assertion wasGeneratedBy ECO_0000203 NP315833.RA8K0h4u1rCqKp2jl3XoU8N2evyLplzkxDZaDXtJBJB5s130_provenance.
- NP315833.RA8K0h4u1rCqKp2jl3XoU8N2evyLplzkxDZaDXtJBJB5s130_assertion wasDerivedFrom befree-20140225 NP315833.RA8K0h4u1rCqKp2jl3XoU8N2evyLplzkxDZaDXtJBJB5s130_provenance.
- NP315833.RA8K0h4u1rCqKp2jl3XoU8N2evyLplzkxDZaDXtJBJB5s130_assertion SIO_000772 17457594 NP315833.RA8K0h4u1rCqKp2jl3XoU8N2evyLplzkxDZaDXtJBJB5s130_provenance.
- NP315833.RA8K0h4u1rCqKp2jl3XoU8N2evyLplzkxDZaDXtJBJB5s130_assertion evidence source_evidence_literature NP315833.RA8K0h4u1rCqKp2jl3XoU8N2evyLplzkxDZaDXtJBJB5s130_provenance.
- NP315833.RA8K0h4u1rCqKp2jl3XoU8N2evyLplzkxDZaDXtJBJB5s130_assertion description "[Frontotemporal dementia with inclusion body myopathy and Paget's disease of bone (IBMPFD) is a rare, autosomal dominant disorder caused by mutations in the gene valosin-containing protein (VCP).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP315833.RA8K0h4u1rCqKp2jl3XoU8N2evyLplzkxDZaDXtJBJB5s130_provenance.