Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP768954.RA9rbYqPYEe7oyx4hHAA-U2pHaQm3M3CtixlX1ToQmlvo130_assertion> ?p ?o ?g. }
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- NP768954.RA9rbYqPYEe7oyx4hHAA-U2pHaQm3M3CtixlX1ToQmlvo130_assertion type Assertion NP768954.RA9rbYqPYEe7oyx4hHAA-U2pHaQm3M3CtixlX1ToQmlvo130_head.
- NP768954.RA9rbYqPYEe7oyx4hHAA-U2pHaQm3M3CtixlX1ToQmlvo130_assertion description "[The CNS pathology is characterized by a novel pattern of ubiquitin pathology distinct from sporadic and familial frontotemporal lobar degeneration with ubiquitin-positive inclusions (FTLD-U) without VCP mutations.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP768954.RA9rbYqPYEe7oyx4hHAA-U2pHaQm3M3CtixlX1ToQmlvo130_provenance.
- NP768954.RA9rbYqPYEe7oyx4hHAA-U2pHaQm3M3CtixlX1ToQmlvo130_assertion evidence source_evidence_literature NP768954.RA9rbYqPYEe7oyx4hHAA-U2pHaQm3M3CtixlX1ToQmlvo130_provenance.
- NP768954.RA9rbYqPYEe7oyx4hHAA-U2pHaQm3M3CtixlX1ToQmlvo130_assertion SIO_000772 17279000 NP768954.RA9rbYqPYEe7oyx4hHAA-U2pHaQm3M3CtixlX1ToQmlvo130_provenance.
- NP768954.RA9rbYqPYEe7oyx4hHAA-U2pHaQm3M3CtixlX1ToQmlvo130_assertion wasDerivedFrom befree-20150227 NP768954.RA9rbYqPYEe7oyx4hHAA-U2pHaQm3M3CtixlX1ToQmlvo130_provenance.
- NP768954.RA9rbYqPYEe7oyx4hHAA-U2pHaQm3M3CtixlX1ToQmlvo130_assertion wasGeneratedBy ECO_0000203 NP768954.RA9rbYqPYEe7oyx4hHAA-U2pHaQm3M3CtixlX1ToQmlvo130_provenance.