Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP1216326.RA2_5c0dHRsbaUo-P2OBMiIQcgauHDk_F1RCVtNxgkDVA130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP1216326.RA2_5c0dHRsbaUo-P2OBMiIQcgauHDk_F1RCVtNxgkDVA130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP1216326.RA2_5c0dHRsbaUo-P2OBMiIQcgauHDk_F1RCVtNxgkDVA130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP1216326.RA2_5c0dHRsbaUo-P2OBMiIQcgauHDk_F1RCVtNxgkDVA130_provenance.
- 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.
- befree-2016 importedOn "2016-02-19" NP1216326.RA2_5c0dHRsbaUo-P2OBMiIQcgauHDk_F1RCVtNxgkDVA130_provenance.