Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP118692.RA7Ja7xLt0vws5nK71Dr0SQqmX9gKTC2W0V2-ETTZk6VM130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP118692.RA7Ja7xLt0vws5nK71Dr0SQqmX9gKTC2W0V2-ETTZk6VM130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP118692.RA7Ja7xLt0vws5nK71Dr0SQqmX9gKTC2W0V2-ETTZk6VM130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP118692.RA7Ja7xLt0vws5nK71Dr0SQqmX9gKTC2W0V2-ETTZk6VM130_provenance.
- NP118692.RA7Ja7xLt0vws5nK71Dr0SQqmX9gKTC2W0V2-ETTZk6VM130_assertion description "[SNP D19H, but not SNP T400K, in the ABCG8 gene is significantly associated with GSD in an Indian population.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP118692.RA7Ja7xLt0vws5nK71Dr0SQqmX9gKTC2W0V2-ETTZk6VM130_provenance.
- NP118692.RA7Ja7xLt0vws5nK71Dr0SQqmX9gKTC2W0V2-ETTZk6VM130_assertion evidence source_evidence_literature NP118692.RA7Ja7xLt0vws5nK71Dr0SQqmX9gKTC2W0V2-ETTZk6VM130_provenance.
- NP118692.RA7Ja7xLt0vws5nK71Dr0SQqmX9gKTC2W0V2-ETTZk6VM130_assertion SIO_000772 20594224 NP118692.RA7Ja7xLt0vws5nK71Dr0SQqmX9gKTC2W0V2-ETTZk6VM130_provenance.
- NP118692.RA7Ja7xLt0vws5nK71Dr0SQqmX9gKTC2W0V2-ETTZk6VM130_assertion wasDerivedFrom gad-20150221 NP118692.RA7Ja7xLt0vws5nK71Dr0SQqmX9gKTC2W0V2-ETTZk6VM130_provenance.
- NP118692.RA7Ja7xLt0vws5nK71Dr0SQqmX9gKTC2W0V2-ETTZk6VM130_assertion wasGeneratedBy ECO_0000203 NP118692.RA7Ja7xLt0vws5nK71Dr0SQqmX9gKTC2W0V2-ETTZk6VM130_provenance.
- gad-20150221 importedOn "2015-02-21" NP118692.RA7Ja7xLt0vws5nK71Dr0SQqmX9gKTC2W0V2-ETTZk6VM130_provenance.