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- source_evidence_literature type ECO_0000212 NP1293227.RA4MWONzChNYpYTMbsSh3HRNlSNo2Xvuj_lc3TiCuwUR4130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP1293227.RA4MWONzChNYpYTMbsSh3HRNlSNo2Xvuj_lc3TiCuwUR4130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP1293227.RA4MWONzChNYpYTMbsSh3HRNlSNo2Xvuj_lc3TiCuwUR4130_provenance.
- NP1293227.RA4MWONzChNYpYTMbsSh3HRNlSNo2Xvuj_lc3TiCuwUR4130_assertion description "[The GGGGCC (G4C2) repeat expansion in a noncoding region of C9orf72 is the most common cause of sporadic and familial forms of amyotrophic lateral sclerosis and frontotemporal dementia.The basis for pathogenesis is unknown.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1293227.RA4MWONzChNYpYTMbsSh3HRNlSNo2Xvuj_lc3TiCuwUR4130_provenance.
- NP1293227.RA4MWONzChNYpYTMbsSh3HRNlSNo2Xvuj_lc3TiCuwUR4130_assertion evidence source_evidence_literature NP1293227.RA4MWONzChNYpYTMbsSh3HRNlSNo2Xvuj_lc3TiCuwUR4130_provenance.
- NP1293227.RA4MWONzChNYpYTMbsSh3HRNlSNo2Xvuj_lc3TiCuwUR4130_assertion SIO_000772 26308899 NP1293227.RA4MWONzChNYpYTMbsSh3HRNlSNo2Xvuj_lc3TiCuwUR4130_provenance.
- NP1293227.RA4MWONzChNYpYTMbsSh3HRNlSNo2Xvuj_lc3TiCuwUR4130_assertion wasDerivedFrom befree-2016 NP1293227.RA4MWONzChNYpYTMbsSh3HRNlSNo2Xvuj_lc3TiCuwUR4130_provenance.
- NP1293227.RA4MWONzChNYpYTMbsSh3HRNlSNo2Xvuj_lc3TiCuwUR4130_assertion wasGeneratedBy ECO_0000203 NP1293227.RA4MWONzChNYpYTMbsSh3HRNlSNo2Xvuj_lc3TiCuwUR4130_provenance.
- befree-2016 importedOn "2016-02-19" NP1293227.RA4MWONzChNYpYTMbsSh3HRNlSNo2Xvuj_lc3TiCuwUR4130_provenance.