Matches in Nanopublications for { <http://rdf.disgenet.org/nanopublications.trig#NP196590.RAnjPXD3iH-9f5nr6BGebvc3QIrHNnYytgT6orPvDLwNA130_assertion> ?p ?o ?g. }
Showing items 1 to 6 of
6
with 100 items per page.
- NP196590.RAnjPXD3iH-9f5nr6BGebvc3QIrHNnYytgT6orPvDLwNA130_assertion type Assertion NP196590.RAnjPXD3iH-9f5nr6BGebvc3QIrHNnYytgT6orPvDLwNA130_head.
- NP196590.RAnjPXD3iH-9f5nr6BGebvc3QIrHNnYytgT6orPvDLwNA130_assertion description "[We propose that familial cortical myoclonus is a novel movement disorder that may be caused by mutation in NOL3.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP196590.RAnjPXD3iH-9f5nr6BGebvc3QIrHNnYytgT6orPvDLwNA130_provenance.
- NP196590.RAnjPXD3iH-9f5nr6BGebvc3QIrHNnYytgT6orPvDLwNA130_assertion evidence source_evidence_literature NP196590.RAnjPXD3iH-9f5nr6BGebvc3QIrHNnYytgT6orPvDLwNA130_provenance.
- NP196590.RAnjPXD3iH-9f5nr6BGebvc3QIrHNnYytgT6orPvDLwNA130_assertion SIO_000772 22926851 NP196590.RAnjPXD3iH-9f5nr6BGebvc3QIrHNnYytgT6orPvDLwNA130_provenance.
- NP196590.RAnjPXD3iH-9f5nr6BGebvc3QIrHNnYytgT6orPvDLwNA130_assertion wasDerivedFrom befree-20140225 NP196590.RAnjPXD3iH-9f5nr6BGebvc3QIrHNnYytgT6orPvDLwNA130_provenance.
- NP196590.RAnjPXD3iH-9f5nr6BGebvc3QIrHNnYytgT6orPvDLwNA130_assertion wasGeneratedBy ECO_0000203 NP196590.RAnjPXD3iH-9f5nr6BGebvc3QIrHNnYytgT6orPvDLwNA130_provenance.