Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP1238556.RA4DJAhVrAowZLnvHU8WPBI3538AMvVNDBMamacl2lTyo130_assertion> ?p ?o ?g. }
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- NP1238556.RA4DJAhVrAowZLnvHU8WPBI3538AMvVNDBMamacl2lTyo130_assertion type Assertion NP1238556.RA4DJAhVrAowZLnvHU8WPBI3538AMvVNDBMamacl2lTyo130_head.
- NP1238556.RA4DJAhVrAowZLnvHU8WPBI3538AMvVNDBMamacl2lTyo130_assertion description "[Its mutant form, P56S-VAPB, which has been linked to a dominantly inherited form of Amyotrophic Lateral Sclerosis (ALS8), generates intracellular inclusions consisting in restructured ER domains whose role in ALS pathogenesis has not been elucidated.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1238556.RA4DJAhVrAowZLnvHU8WPBI3538AMvVNDBMamacl2lTyo130_provenance.
- NP1238556.RA4DJAhVrAowZLnvHU8WPBI3538AMvVNDBMamacl2lTyo130_assertion evidence source_evidence_literature NP1238556.RA4DJAhVrAowZLnvHU8WPBI3538AMvVNDBMamacl2lTyo130_provenance.
- NP1238556.RA4DJAhVrAowZLnvHU8WPBI3538AMvVNDBMamacl2lTyo130_assertion SIO_000772 25409455 NP1238556.RA4DJAhVrAowZLnvHU8WPBI3538AMvVNDBMamacl2lTyo130_provenance.
- NP1238556.RA4DJAhVrAowZLnvHU8WPBI3538AMvVNDBMamacl2lTyo130_assertion wasDerivedFrom befree-2016 NP1238556.RA4DJAhVrAowZLnvHU8WPBI3538AMvVNDBMamacl2lTyo130_provenance.
- NP1238556.RA4DJAhVrAowZLnvHU8WPBI3538AMvVNDBMamacl2lTyo130_assertion wasGeneratedBy ECO_0000203 NP1238556.RA4DJAhVrAowZLnvHU8WPBI3538AMvVNDBMamacl2lTyo130_provenance.