Matches in Nanopublications for { <http://rdf.disgenet.org/nanopublications.trig#NP357247.RAJNvY7Tpih00VTr-t0dqp6QE8hR6bbN_Mi-vby2XM2Bo130_assertion> ?p ?o ?g. }
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- NP357247.RAJNvY7Tpih00VTr-t0dqp6QE8hR6bbN_Mi-vby2XM2Bo130_assertion type Assertion NP357247.RAJNvY7Tpih00VTr-t0dqp6QE8hR6bbN_Mi-vby2XM2Bo130_head.
- NP357247.RAJNvY7Tpih00VTr-t0dqp6QE8hR6bbN_Mi-vby2XM2Bo130_assertion description "[Mutations in the valosin-containing protein (VCP) gene on chromosome 9p13-p12 recently have been shown to cause autosomal dominant inclusion body myopathy associated with Paget's disease of the bone and frontotemporal dementia.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP357247.RAJNvY7Tpih00VTr-t0dqp6QE8hR6bbN_Mi-vby2XM2Bo130_provenance.
- NP357247.RAJNvY7Tpih00VTr-t0dqp6QE8hR6bbN_Mi-vby2XM2Bo130_assertion evidence source_evidence_literature NP357247.RAJNvY7Tpih00VTr-t0dqp6QE8hR6bbN_Mi-vby2XM2Bo130_provenance.
- NP357247.RAJNvY7Tpih00VTr-t0dqp6QE8hR6bbN_Mi-vby2XM2Bo130_assertion SIO_000772 15732117 NP357247.RAJNvY7Tpih00VTr-t0dqp6QE8hR6bbN_Mi-vby2XM2Bo130_provenance.
- NP357247.RAJNvY7Tpih00VTr-t0dqp6QE8hR6bbN_Mi-vby2XM2Bo130_assertion wasDerivedFrom befree-20140225 NP357247.RAJNvY7Tpih00VTr-t0dqp6QE8hR6bbN_Mi-vby2XM2Bo130_provenance.
- NP357247.RAJNvY7Tpih00VTr-t0dqp6QE8hR6bbN_Mi-vby2XM2Bo130_assertion wasGeneratedBy ECO_0000203 NP357247.RAJNvY7Tpih00VTr-t0dqp6QE8hR6bbN_Mi-vby2XM2Bo130_provenance.