Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP1216326.RA2_5c0dHRsbaUo-P2OBMiIQcgauHDk_F1RCVtNxgkDVA130_assertion> ?p ?o ?g. }
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- NP1216326.RA2_5c0dHRsbaUo-P2OBMiIQcgauHDk_F1RCVtNxgkDVA130_assertion type Assertion NP1216326.RA2_5c0dHRsbaUo-P2OBMiIQcgauHDk_F1RCVtNxgkDVA130_head.
- NP1216326.RA2_5c0dHRsbaUo-P2OBMiIQcgauHDk_F1RCVtNxgkDVA130_assertion description "[Co-occurrence of the C9ORF72 expansion and a novel GRN mutation in a family with alternative expression of frontotemporal dementia and amyotrophic lateral sclerosis.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1216326.RA2_5c0dHRsbaUo-P2OBMiIQcgauHDk_F1RCVtNxgkDVA130_provenance.
- NP1216326.RA2_5c0dHRsbaUo-P2OBMiIQcgauHDk_F1RCVtNxgkDVA130_assertion evidence source_evidence_literature NP1216326.RA2_5c0dHRsbaUo-P2OBMiIQcgauHDk_F1RCVtNxgkDVA130_provenance.
- NP1216326.RA2_5c0dHRsbaUo-P2OBMiIQcgauHDk_F1RCVtNxgkDVA130_assertion SIO_000772 25182743 NP1216326.RA2_5c0dHRsbaUo-P2OBMiIQcgauHDk_F1RCVtNxgkDVA130_provenance.
- NP1216326.RA2_5c0dHRsbaUo-P2OBMiIQcgauHDk_F1RCVtNxgkDVA130_assertion wasDerivedFrom befree-2016 NP1216326.RA2_5c0dHRsbaUo-P2OBMiIQcgauHDk_F1RCVtNxgkDVA130_provenance.
- NP1216326.RA2_5c0dHRsbaUo-P2OBMiIQcgauHDk_F1RCVtNxgkDVA130_assertion wasGeneratedBy ECO_0000203 NP1216326.RA2_5c0dHRsbaUo-P2OBMiIQcgauHDk_F1RCVtNxgkDVA130_provenance.