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- source_evidence_literature type ECO_0000212 NP586817.RAAL2lVnSDfTcdLwMAKDPEtpqX3R670a6YFwf-5dkWmeA130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP586817.RAAL2lVnSDfTcdLwMAKDPEtpqX3R670a6YFwf-5dkWmeA130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP586817.RAAL2lVnSDfTcdLwMAKDPEtpqX3R670a6YFwf-5dkWmeA130_provenance.
- NP586817.RAAL2lVnSDfTcdLwMAKDPEtpqX3R670a6YFwf-5dkWmeA130_assertion description "[Furthermore, torsinA, that is mutated in DYT1 dystonia, a rare type of primary dystonia, binds to and promotes the degradation of epsilon-sarcoglycan mutants when both proteins are co-expressed.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP586817.RAAL2lVnSDfTcdLwMAKDPEtpqX3R670a6YFwf-5dkWmeA130_provenance.
- NP586817.RAAL2lVnSDfTcdLwMAKDPEtpqX3R670a6YFwf-5dkWmeA130_assertion evidence source_evidence_literature NP586817.RAAL2lVnSDfTcdLwMAKDPEtpqX3R670a6YFwf-5dkWmeA130_provenance.
- NP586817.RAAL2lVnSDfTcdLwMAKDPEtpqX3R670a6YFwf-5dkWmeA130_assertion SIO_000772 17200151 NP586817.RAAL2lVnSDfTcdLwMAKDPEtpqX3R670a6YFwf-5dkWmeA130_provenance.
- NP586817.RAAL2lVnSDfTcdLwMAKDPEtpqX3R670a6YFwf-5dkWmeA130_assertion wasDerivedFrom befree-2016 NP586817.RAAL2lVnSDfTcdLwMAKDPEtpqX3R670a6YFwf-5dkWmeA130_provenance.
- NP586817.RAAL2lVnSDfTcdLwMAKDPEtpqX3R670a6YFwf-5dkWmeA130_assertion wasGeneratedBy ECO_0000203 NP586817.RAAL2lVnSDfTcdLwMAKDPEtpqX3R670a6YFwf-5dkWmeA130_provenance.
- befree-2016 importedOn "2016-02-19" NP586817.RAAL2lVnSDfTcdLwMAKDPEtpqX3R670a6YFwf-5dkWmeA130_provenance.