Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP702988.RAtdygxTkHOU-rDEsDDx-Hr3jAMVc_28PS5qrGkEb-MfQ130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP702988.RAtdygxTkHOU-rDEsDDx-Hr3jAMVc_28PS5qrGkEb-MfQ130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP702988.RAtdygxTkHOU-rDEsDDx-Hr3jAMVc_28PS5qrGkEb-MfQ130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP702988.RAtdygxTkHOU-rDEsDDx-Hr3jAMVc_28PS5qrGkEb-MfQ130_provenance.
- NP702988.RAtdygxTkHOU-rDEsDDx-Hr3jAMVc_28PS5qrGkEb-MfQ130_assertion description "[Also, a variant SYT-SSX4 fusion gene has recently been shown in a single SS case.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP702988.RAtdygxTkHOU-rDEsDDx-Hr3jAMVc_28PS5qrGkEb-MfQ130_provenance.
- NP702988.RAtdygxTkHOU-rDEsDDx-Hr3jAMVc_28PS5qrGkEb-MfQ130_assertion evidence source_evidence_literature NP702988.RAtdygxTkHOU-rDEsDDx-Hr3jAMVc_28PS5qrGkEb-MfQ130_provenance.
- NP702988.RAtdygxTkHOU-rDEsDDx-Hr3jAMVc_28PS5qrGkEb-MfQ130_assertion SIO_000772 10879732 NP702988.RAtdygxTkHOU-rDEsDDx-Hr3jAMVc_28PS5qrGkEb-MfQ130_provenance.
- NP702988.RAtdygxTkHOU-rDEsDDx-Hr3jAMVc_28PS5qrGkEb-MfQ130_assertion wasDerivedFrom befree-20140225 NP702988.RAtdygxTkHOU-rDEsDDx-Hr3jAMVc_28PS5qrGkEb-MfQ130_provenance.
- NP702988.RAtdygxTkHOU-rDEsDDx-Hr3jAMVc_28PS5qrGkEb-MfQ130_assertion wasGeneratedBy ECO_0000203 NP702988.RAtdygxTkHOU-rDEsDDx-Hr3jAMVc_28PS5qrGkEb-MfQ130_provenance.
- befree-20140225 importedOn "2014-02-25" NP702988.RAtdygxTkHOU-rDEsDDx-Hr3jAMVc_28PS5qrGkEb-MfQ130_provenance.