Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP183876.RA4U3hGUvEaENieaoS3zGht23LT-Vfi9hvSxvcArN0gtI130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP183876.RA4U3hGUvEaENieaoS3zGht23LT-Vfi9hvSxvcArN0gtI130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP183876.RA4U3hGUvEaENieaoS3zGht23LT-Vfi9hvSxvcArN0gtI130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP183876.RA4U3hGUvEaENieaoS3zGht23LT-Vfi9hvSxvcArN0gtI130_provenance.
- NP183876.RA4U3hGUvEaENieaoS3zGht23LT-Vfi9hvSxvcArN0gtI130_assertion description "[Variation in folate pathway genes contributes to risk of congenital heart defects among individuals with Down syndrome.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP183876.RA4U3hGUvEaENieaoS3zGht23LT-Vfi9hvSxvcArN0gtI130_provenance.
- NP183876.RA4U3hGUvEaENieaoS3zGht23LT-Vfi9hvSxvcArN0gtI130_assertion evidence source_evidence_literature NP183876.RA4U3hGUvEaENieaoS3zGht23LT-Vfi9hvSxvcArN0gtI130_provenance.
- NP183876.RA4U3hGUvEaENieaoS3zGht23LT-Vfi9hvSxvcArN0gtI130_assertion SIO_000772 20718043 NP183876.RA4U3hGUvEaENieaoS3zGht23LT-Vfi9hvSxvcArN0gtI130_provenance.
- NP183876.RA4U3hGUvEaENieaoS3zGht23LT-Vfi9hvSxvcArN0gtI130_assertion wasDerivedFrom gad-20150221 NP183876.RA4U3hGUvEaENieaoS3zGht23LT-Vfi9hvSxvcArN0gtI130_provenance.
- NP183876.RA4U3hGUvEaENieaoS3zGht23LT-Vfi9hvSxvcArN0gtI130_assertion wasGeneratedBy ECO_0000203 NP183876.RA4U3hGUvEaENieaoS3zGht23LT-Vfi9hvSxvcArN0gtI130_provenance.
- gad-20150221 importedOn "2015-02-21" NP183876.RA4U3hGUvEaENieaoS3zGht23LT-Vfi9hvSxvcArN0gtI130_provenance.