Matches in Nanopublications for { <http://rdf.disgenet.org/nanopublications.trig#NP241973.RAzKH-zsiMganY6ZsB3bQdSGgCYxrWBKAC0drluzpT5k0130_assertion> ?p ?o ?g. }
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- NP241973.RAzKH-zsiMganY6ZsB3bQdSGgCYxrWBKAC0drluzpT5k0130_assertion type Assertion NP241973.RAzKH-zsiMganY6ZsB3bQdSGgCYxrWBKAC0drluzpT5k0130_head.
- NP241973.RAzKH-zsiMganY6ZsB3bQdSGgCYxrWBKAC0drluzpT5k0130_assertion description "[The frequency of UBQLN2 and PFN1 genetic variants in the FTLD patients was low at 0.30% and 0.91% respectively.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP241973.RAzKH-zsiMganY6ZsB3bQdSGgCYxrWBKAC0drluzpT5k0130_provenance.
- NP241973.RAzKH-zsiMganY6ZsB3bQdSGgCYxrWBKAC0drluzpT5k0130_assertion evidence source_evidence_literature NP241973.RAzKH-zsiMganY6ZsB3bQdSGgCYxrWBKAC0drluzpT5k0130_provenance.
- NP241973.RAzKH-zsiMganY6ZsB3bQdSGgCYxrWBKAC0drluzpT5k0130_assertion SIO_000772 23312802 NP241973.RAzKH-zsiMganY6ZsB3bQdSGgCYxrWBKAC0drluzpT5k0130_provenance.
- NP241973.RAzKH-zsiMganY6ZsB3bQdSGgCYxrWBKAC0drluzpT5k0130_assertion wasDerivedFrom befree-20140225 NP241973.RAzKH-zsiMganY6ZsB3bQdSGgCYxrWBKAC0drluzpT5k0130_provenance.
- NP241973.RAzKH-zsiMganY6ZsB3bQdSGgCYxrWBKAC0drluzpT5k0130_assertion wasGeneratedBy ECO_0000203 NP241973.RAzKH-zsiMganY6ZsB3bQdSGgCYxrWBKAC0drluzpT5k0130_provenance.