Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP453249.RAxG5pi09zhRdGj2g0tmrRqfWIs-07XUBONqjaNPn6ZIo130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP453249.RAxG5pi09zhRdGj2g0tmrRqfWIs-07XUBONqjaNPn6ZIo130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP453249.RAxG5pi09zhRdGj2g0tmrRqfWIs-07XUBONqjaNPn6ZIo130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP453249.RAxG5pi09zhRdGj2g0tmrRqfWIs-07XUBONqjaNPn6ZIo130_provenance.
- NP453249.RAxG5pi09zhRdGj2g0tmrRqfWIs-07XUBONqjaNPn6ZIo130_assertion description "[Heterozygous mutations of the GCK gene may result in neonatal diabetes similar to type 1 diabetes, the cause of such phenotype variety is still unknown.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP453249.RAxG5pi09zhRdGj2g0tmrRqfWIs-07XUBONqjaNPn6ZIo130_provenance.
- NP453249.RAxG5pi09zhRdGj2g0tmrRqfWIs-07XUBONqjaNPn6ZIo130_assertion evidence source_evidence_literature NP453249.RAxG5pi09zhRdGj2g0tmrRqfWIs-07XUBONqjaNPn6ZIo130_provenance.
- NP453249.RAxG5pi09zhRdGj2g0tmrRqfWIs-07XUBONqjaNPn6ZIo130_assertion SIO_000772 21437567 NP453249.RAxG5pi09zhRdGj2g0tmrRqfWIs-07XUBONqjaNPn6ZIo130_provenance.
- NP453249.RAxG5pi09zhRdGj2g0tmrRqfWIs-07XUBONqjaNPn6ZIo130_assertion wasDerivedFrom befree-20140225 NP453249.RAxG5pi09zhRdGj2g0tmrRqfWIs-07XUBONqjaNPn6ZIo130_provenance.
- NP453249.RAxG5pi09zhRdGj2g0tmrRqfWIs-07XUBONqjaNPn6ZIo130_assertion wasGeneratedBy ECO_0000203 NP453249.RAxG5pi09zhRdGj2g0tmrRqfWIs-07XUBONqjaNPn6ZIo130_provenance.
- befree-20140225 importedOn "2014-02-25" NP453249.RAxG5pi09zhRdGj2g0tmrRqfWIs-07XUBONqjaNPn6ZIo130_provenance.