Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP1137369.RAas4JHYKeoSFkr6ysnlDPGtyTLOtcgSLg7q0HMPgelDM130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP1137369.RAas4JHYKeoSFkr6ysnlDPGtyTLOtcgSLg7q0HMPgelDM130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP1137369.RAas4JHYKeoSFkr6ysnlDPGtyTLOtcgSLg7q0HMPgelDM130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP1137369.RAas4JHYKeoSFkr6ysnlDPGtyTLOtcgSLg7q0HMPgelDM130_provenance.
- NP1137369.RAas4JHYKeoSFkr6ysnlDPGtyTLOtcgSLg7q0HMPgelDM130_assertion description "[Mutations of the DCTN1 gene have been previously associated with amyotrophic lateral sclerosis and with Perry syndrome, a rare autosomal dominant disorder characterized by weight loss, parkinsonism, central hypoventilation, and psychiatric disturbances.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1137369.RAas4JHYKeoSFkr6ysnlDPGtyTLOtcgSLg7q0HMPgelDM130_provenance.
- NP1137369.RAas4JHYKeoSFkr6ysnlDPGtyTLOtcgSLg7q0HMPgelDM130_assertion evidence source_evidence_literature NP1137369.RAas4JHYKeoSFkr6ysnlDPGtyTLOtcgSLg7q0HMPgelDM130_provenance.
- NP1137369.RAas4JHYKeoSFkr6ysnlDPGtyTLOtcgSLg7q0HMPgelDM130_assertion SIO_000772 24343258 NP1137369.RAas4JHYKeoSFkr6ysnlDPGtyTLOtcgSLg7q0HMPgelDM130_provenance.
- NP1137369.RAas4JHYKeoSFkr6ysnlDPGtyTLOtcgSLg7q0HMPgelDM130_assertion wasDerivedFrom befree-2016 NP1137369.RAas4JHYKeoSFkr6ysnlDPGtyTLOtcgSLg7q0HMPgelDM130_provenance.
- NP1137369.RAas4JHYKeoSFkr6ysnlDPGtyTLOtcgSLg7q0HMPgelDM130_assertion wasGeneratedBy ECO_0000203 NP1137369.RAas4JHYKeoSFkr6ysnlDPGtyTLOtcgSLg7q0HMPgelDM130_provenance.
- befree-2016 importedOn "2016-02-19" NP1137369.RAas4JHYKeoSFkr6ysnlDPGtyTLOtcgSLg7q0HMPgelDM130_provenance.