Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP307546.RACza8hYkEtffRSQcnetdvAq3K6BB2SW3Iq4cfqQ2Mtbc130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP307546.RACza8hYkEtffRSQcnetdvAq3K6BB2SW3Iq4cfqQ2Mtbc130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP307546.RACza8hYkEtffRSQcnetdvAq3K6BB2SW3Iq4cfqQ2Mtbc130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP307546.RACza8hYkEtffRSQcnetdvAq3K6BB2SW3Iq4cfqQ2Mtbc130_provenance.
- NP307546.RACza8hYkEtffRSQcnetdvAq3K6BB2SW3Iq4cfqQ2Mtbc130_assertion description "[All four familial cases of BWS showed reduced methylation of KCNQ1OT1, suggesting that in these cases the imprinting switch mechanism is disturbed.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP307546.RACza8hYkEtffRSQcnetdvAq3K6BB2SW3Iq4cfqQ2Mtbc130_provenance.
- NP307546.RACza8hYkEtffRSQcnetdvAq3K6BB2SW3Iq4cfqQ2Mtbc130_assertion evidence source_evidence_literature NP307546.RACza8hYkEtffRSQcnetdvAq3K6BB2SW3Iq4cfqQ2Mtbc130_provenance.
- NP307546.RACza8hYkEtffRSQcnetdvAq3K6BB2SW3Iq4cfqQ2Mtbc130_assertion SIO_000772 11181570 NP307546.RACza8hYkEtffRSQcnetdvAq3K6BB2SW3Iq4cfqQ2Mtbc130_provenance.
- NP307546.RACza8hYkEtffRSQcnetdvAq3K6BB2SW3Iq4cfqQ2Mtbc130_assertion wasDerivedFrom befree-2016 NP307546.RACza8hYkEtffRSQcnetdvAq3K6BB2SW3Iq4cfqQ2Mtbc130_provenance.
- NP307546.RACza8hYkEtffRSQcnetdvAq3K6BB2SW3Iq4cfqQ2Mtbc130_assertion wasGeneratedBy ECO_0000203 NP307546.RACza8hYkEtffRSQcnetdvAq3K6BB2SW3Iq4cfqQ2Mtbc130_provenance.
- befree-2016 importedOn "2016-02-19" NP307546.RACza8hYkEtffRSQcnetdvAq3K6BB2SW3Iq4cfqQ2Mtbc130_provenance.