Matches in Nanopublications for { <http://rdf.disgenet.org/nanopublications.trig#NP885627.RAJ1uM4Xf82FMiJoLwHKTMyo3bkQPGSI0EtJCDI9v3zhU130_assertion> ?p ?o ?g. }
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- NP885627.RAJ1uM4Xf82FMiJoLwHKTMyo3bkQPGSI0EtJCDI9v3zhU130_assertion type Assertion NP885627.RAJ1uM4Xf82FMiJoLwHKTMyo3bkQPGSI0EtJCDI9v3zhU130_head.
- NP885627.RAJ1uM4Xf82FMiJoLwHKTMyo3bkQPGSI0EtJCDI9v3zhU130_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." NP885627.RAJ1uM4Xf82FMiJoLwHKTMyo3bkQPGSI0EtJCDI9v3zhU130_provenance.
- NP885627.RAJ1uM4Xf82FMiJoLwHKTMyo3bkQPGSI0EtJCDI9v3zhU130_assertion evidence source_evidence_literature NP885627.RAJ1uM4Xf82FMiJoLwHKTMyo3bkQPGSI0EtJCDI9v3zhU130_provenance.
- NP885627.RAJ1uM4Xf82FMiJoLwHKTMyo3bkQPGSI0EtJCDI9v3zhU130_assertion SIO_000772 15732117 NP885627.RAJ1uM4Xf82FMiJoLwHKTMyo3bkQPGSI0EtJCDI9v3zhU130_provenance.
- NP885627.RAJ1uM4Xf82FMiJoLwHKTMyo3bkQPGSI0EtJCDI9v3zhU130_assertion wasDerivedFrom befree-20140225 NP885627.RAJ1uM4Xf82FMiJoLwHKTMyo3bkQPGSI0EtJCDI9v3zhU130_provenance.
- NP885627.RAJ1uM4Xf82FMiJoLwHKTMyo3bkQPGSI0EtJCDI9v3zhU130_assertion wasGeneratedBy ECO_0000203 NP885627.RAJ1uM4Xf82FMiJoLwHKTMyo3bkQPGSI0EtJCDI9v3zhU130_provenance.