Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP690756.RABix091wlDnB_0KLBEYy-eLz2S4bSVWg_tWGrwvvt6VY130_assertion> ?p ?o ?g. }
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- NP690756.RABix091wlDnB_0KLBEYy-eLz2S4bSVWg_tWGrwvvt6VY130_assertion type Assertion NP690756.RABix091wlDnB_0KLBEYy-eLz2S4bSVWg_tWGrwvvt6VY130_head.
- NP690756.RABix091wlDnB_0KLBEYy-eLz2S4bSVWg_tWGrwvvt6VY130_assertion description "[The present findings, together with a previous negative study on MAPT and SOD1 mutation, further elucidated the lack of causative mutations in all exons, exon-intron boundaries, or some rearrangements of the reported major causative or susceptible genes related to ALS, FTLD, parkinsonism, synucleinopathy, TDP-43 proteinopathy, and tauopathy.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP690756.RABix091wlDnB_0KLBEYy-eLz2S4bSVWg_tWGrwvvt6VY130_provenance.
- NP690756.RABix091wlDnB_0KLBEYy-eLz2S4bSVWg_tWGrwvvt6VY130_assertion evidence source_evidence_literature NP690756.RABix091wlDnB_0KLBEYy-eLz2S4bSVWg_tWGrwvvt6VY130_provenance.
- NP690756.RABix091wlDnB_0KLBEYy-eLz2S4bSVWg_tWGrwvvt6VY130_assertion SIO_000772 18759352 NP690756.RABix091wlDnB_0KLBEYy-eLz2S4bSVWg_tWGrwvvt6VY130_provenance.
- NP690756.RABix091wlDnB_0KLBEYy-eLz2S4bSVWg_tWGrwvvt6VY130_assertion wasDerivedFrom befree-2016 NP690756.RABix091wlDnB_0KLBEYy-eLz2S4bSVWg_tWGrwvvt6VY130_provenance.
- NP690756.RABix091wlDnB_0KLBEYy-eLz2S4bSVWg_tWGrwvvt6VY130_assertion wasGeneratedBy ECO_0000203 NP690756.RABix091wlDnB_0KLBEYy-eLz2S4bSVWg_tWGrwvvt6VY130_provenance.