Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP646097.RA0eWoJ9nwLL0jdap2ZET5eFZPW4e1J52iCmD-Ze5vzI0130_assertion> ?p ?o ?g. }
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- NP646097.RA0eWoJ9nwLL0jdap2ZET5eFZPW4e1J52iCmD-Ze5vzI0130_assertion type Assertion NP646097.RA0eWoJ9nwLL0jdap2ZET5eFZPW4e1J52iCmD-Ze5vzI0130_head.
- NP646097.RA0eWoJ9nwLL0jdap2ZET5eFZPW4e1J52iCmD-Ze5vzI0130_assertion description "[A number of families have been reported with autosomal dominant FTD-ALS linked to chromosome 9p and these also have TDP-43-positive frontotemporal lobar degeneration with ubiquitinated inclusions pathology.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP646097.RA0eWoJ9nwLL0jdap2ZET5eFZPW4e1J52iCmD-Ze5vzI0130_provenance.
- NP646097.RA0eWoJ9nwLL0jdap2ZET5eFZPW4e1J52iCmD-Ze5vzI0130_assertion evidence source_evidence_literature NP646097.RA0eWoJ9nwLL0jdap2ZET5eFZPW4e1J52iCmD-Ze5vzI0130_provenance.
- NP646097.RA0eWoJ9nwLL0jdap2ZET5eFZPW4e1J52iCmD-Ze5vzI0130_assertion SIO_000772 18090423 NP646097.RA0eWoJ9nwLL0jdap2ZET5eFZPW4e1J52iCmD-Ze5vzI0130_provenance.
- NP646097.RA0eWoJ9nwLL0jdap2ZET5eFZPW4e1J52iCmD-Ze5vzI0130_assertion wasDerivedFrom befree-2016 NP646097.RA0eWoJ9nwLL0jdap2ZET5eFZPW4e1J52iCmD-Ze5vzI0130_provenance.
- NP646097.RA0eWoJ9nwLL0jdap2ZET5eFZPW4e1J52iCmD-Ze5vzI0130_assertion wasGeneratedBy ECO_0000203 NP646097.RA0eWoJ9nwLL0jdap2ZET5eFZPW4e1J52iCmD-Ze5vzI0130_provenance.