Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP224573.RAC_njpUyHsGS7HgyJw7oBwwVXz58ovaeiW7FtVSUdu4M130_assertion> ?p ?o ?g. }
Showing items 1 to 6 of
6
with 100 items per page.
- NP224573.RAC_njpUyHsGS7HgyJw7oBwwVXz58ovaeiW7FtVSUdu4M130_assertion type Assertion NP224573.RAC_njpUyHsGS7HgyJw7oBwwVXz58ovaeiW7FtVSUdu4M130_head.
- NP224573.RAC_njpUyHsGS7HgyJw7oBwwVXz58ovaeiW7FtVSUdu4M130_assertion wasGeneratedBy ECO_0000203 NP224573.RAC_njpUyHsGS7HgyJw7oBwwVXz58ovaeiW7FtVSUdu4M130_provenance.
- NP224573.RAC_njpUyHsGS7HgyJw7oBwwVXz58ovaeiW7FtVSUdu4M130_assertion wasDerivedFrom lhgdn-20090331 NP224573.RAC_njpUyHsGS7HgyJw7oBwwVXz58ovaeiW7FtVSUdu4M130_provenance.
- NP224573.RAC_njpUyHsGS7HgyJw7oBwwVXz58ovaeiW7FtVSUdu4M130_assertion SIO_000772 17457594 NP224573.RAC_njpUyHsGS7HgyJw7oBwwVXz58ovaeiW7FtVSUdu4M130_provenance.
- NP224573.RAC_njpUyHsGS7HgyJw7oBwwVXz58ovaeiW7FtVSUdu4M130_assertion evidence source_evidence_literature NP224573.RAC_njpUyHsGS7HgyJw7oBwwVXz58ovaeiW7FtVSUdu4M130_provenance.
- NP224573.RAC_njpUyHsGS7HgyJw7oBwwVXz58ovaeiW7FtVSUdu4M130_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." NP224573.RAC_njpUyHsGS7HgyJw7oBwwVXz58ovaeiW7FtVSUdu4M130_provenance.