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- source_evidence_literature type ECO_0000212 NP895447.RACcMJWQ_ogB-AL-EPbrh-ItLuSh8U0Sp2SGrP7y55Hqc130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP895447.RACcMJWQ_ogB-AL-EPbrh-ItLuSh8U0Sp2SGrP7y55Hqc130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP895447.RACcMJWQ_ogB-AL-EPbrh-ItLuSh8U0Sp2SGrP7y55Hqc130_provenance.
- NP895447.RACcMJWQ_ogB-AL-EPbrh-ItLuSh8U0Sp2SGrP7y55Hqc130_assertion description "[Mutations in the UBQLN2 and SIGMAR1 genes were recently identified in X-linked dominant amyotrophic lateral sclerosis and/or frontotemporal dementia (ALS and/or FTD) and FTD and/or motor neuron disease, respectively.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP895447.RACcMJWQ_ogB-AL-EPbrh-ItLuSh8U0Sp2SGrP7y55Hqc130_provenance.
- NP895447.RACcMJWQ_ogB-AL-EPbrh-ItLuSh8U0Sp2SGrP7y55Hqc130_assertion evidence source_evidence_literature NP895447.RACcMJWQ_ogB-AL-EPbrh-ItLuSh8U0Sp2SGrP7y55Hqc130_provenance.
- NP895447.RACcMJWQ_ogB-AL-EPbrh-ItLuSh8U0Sp2SGrP7y55Hqc130_assertion SIO_000772 24684794 NP895447.RACcMJWQ_ogB-AL-EPbrh-ItLuSh8U0Sp2SGrP7y55Hqc130_provenance.
- NP895447.RACcMJWQ_ogB-AL-EPbrh-ItLuSh8U0Sp2SGrP7y55Hqc130_assertion wasDerivedFrom befree-20150227 NP895447.RACcMJWQ_ogB-AL-EPbrh-ItLuSh8U0Sp2SGrP7y55Hqc130_provenance.
- NP895447.RACcMJWQ_ogB-AL-EPbrh-ItLuSh8U0Sp2SGrP7y55Hqc130_assertion wasGeneratedBy ECO_0000203 NP895447.RACcMJWQ_ogB-AL-EPbrh-ItLuSh8U0Sp2SGrP7y55Hqc130_provenance.
- befree-20150227 importedOn "2015-02-27" NP895447.RACcMJWQ_ogB-AL-EPbrh-ItLuSh8U0Sp2SGrP7y55Hqc130_provenance.