Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP486239.RAykL5MXFojA9eRwx6Myx2A3cNZwhjFXrPmUWL5iplI0o130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP486239.RAykL5MXFojA9eRwx6Myx2A3cNZwhjFXrPmUWL5iplI0o130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP486239.RAykL5MXFojA9eRwx6Myx2A3cNZwhjFXrPmUWL5iplI0o130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP486239.RAykL5MXFojA9eRwx6Myx2A3cNZwhjFXrPmUWL5iplI0o130_provenance.
- NP486239.RAykL5MXFojA9eRwx6Myx2A3cNZwhjFXrPmUWL5iplI0o130_assertion description "[These data suggest a potential role of the KIR2DL2-rs2756923 polymorphism in T1D in Germans and Belgians.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP486239.RAykL5MXFojA9eRwx6Myx2A3cNZwhjFXrPmUWL5iplI0o130_provenance.
- NP486239.RAykL5MXFojA9eRwx6Myx2A3cNZwhjFXrPmUWL5iplI0o130_assertion evidence source_evidence_literature NP486239.RAykL5MXFojA9eRwx6Myx2A3cNZwhjFXrPmUWL5iplI0o130_provenance.
- NP486239.RAykL5MXFojA9eRwx6Myx2A3cNZwhjFXrPmUWL5iplI0o130_assertion SIO_000772 19392800 NP486239.RAykL5MXFojA9eRwx6Myx2A3cNZwhjFXrPmUWL5iplI0o130_provenance.
- NP486239.RAykL5MXFojA9eRwx6Myx2A3cNZwhjFXrPmUWL5iplI0o130_assertion wasDerivedFrom befree-20140225 NP486239.RAykL5MXFojA9eRwx6Myx2A3cNZwhjFXrPmUWL5iplI0o130_provenance.
- NP486239.RAykL5MXFojA9eRwx6Myx2A3cNZwhjFXrPmUWL5iplI0o130_assertion wasGeneratedBy ECO_0000203 NP486239.RAykL5MXFojA9eRwx6Myx2A3cNZwhjFXrPmUWL5iplI0o130_provenance.
- befree-20140225 importedOn "2014-02-25" NP486239.RAykL5MXFojA9eRwx6Myx2A3cNZwhjFXrPmUWL5iplI0o130_provenance.