Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP147969.RAIayXTpVPKYcaDy9Jevg6zrk08E67Cz9NKmyOEM7z4J0130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP147969.RAIayXTpVPKYcaDy9Jevg6zrk08E67Cz9NKmyOEM7z4J0130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP147969.RAIayXTpVPKYcaDy9Jevg6zrk08E67Cz9NKmyOEM7z4J0130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP147969.RAIayXTpVPKYcaDy9Jevg6zrk08E67Cz9NKmyOEM7z4J0130_provenance.
- NP147969.RAIayXTpVPKYcaDy9Jevg6zrk08E67Cz9NKmyOEM7z4J0130_assertion wasGeneratedBy ECO_0000203 NP147969.RAIayXTpVPKYcaDy9Jevg6zrk08E67Cz9NKmyOEM7z4J0130_provenance.
- NP147969.RAIayXTpVPKYcaDy9Jevg6zrk08E67Cz9NKmyOEM7z4J0130_assertion wasDerivedFrom lhgdn-20090331 NP147969.RAIayXTpVPKYcaDy9Jevg6zrk08E67Cz9NKmyOEM7z4J0130_provenance.
- NP147969.RAIayXTpVPKYcaDy9Jevg6zrk08E67Cz9NKmyOEM7z4J0130_assertion SIO_000772 16332676 NP147969.RAIayXTpVPKYcaDy9Jevg6zrk08E67Cz9NKmyOEM7z4J0130_provenance.
- NP147969.RAIayXTpVPKYcaDy9Jevg6zrk08E67Cz9NKmyOEM7z4J0130_assertion evidence source_evidence_literature NP147969.RAIayXTpVPKYcaDy9Jevg6zrk08E67Cz9NKmyOEM7z4J0130_provenance.
- NP147969.RAIayXTpVPKYcaDy9Jevg6zrk08E67Cz9NKmyOEM7z4J0130_assertion description "[identification of a novel KCNJ11 mutation associated with congenital hyperinsulinism that renders a missense mutation, F55L, in the Kir6.2 protein.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP147969.RAIayXTpVPKYcaDy9Jevg6zrk08E67Cz9NKmyOEM7z4J0130_provenance.
- lhgdn-20090331 importedOn "2009-03-31" NP147969.RAIayXTpVPKYcaDy9Jevg6zrk08E67Cz9NKmyOEM7z4J0130_provenance.