Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP90351.RAVX7EvruVNq5HlhWY2TOefL7wiknXYZByjqu1OD3EZfc130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP90351.RAVX7EvruVNq5HlhWY2TOefL7wiknXYZByjqu1OD3EZfc130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP90351.RAVX7EvruVNq5HlhWY2TOefL7wiknXYZByjqu1OD3EZfc130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP90351.RAVX7EvruVNq5HlhWY2TOefL7wiknXYZByjqu1OD3EZfc130_provenance.
- NP90351.RAVX7EvruVNq5HlhWY2TOefL7wiknXYZByjqu1OD3EZfc130_assertion description "[ The rare CX3CR1 alleles were associated with an increased risk of BI and with reduced frequency of cardiovascular history. We propose that the extra adhesion of monocytes observed in individuals carrying rare alleles of CX3CR1 may favor mechanisms leadin]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP90351.RAVX7EvruVNq5HlhWY2TOefL7wiknXYZByjqu1OD3EZfc130_provenance.
- NP90351.RAVX7EvruVNq5HlhWY2TOefL7wiknXYZByjqu1OD3EZfc130_assertion evidence source_evidence_literature NP90351.RAVX7EvruVNq5HlhWY2TOefL7wiknXYZByjqu1OD3EZfc130_provenance.
- NP90351.RAVX7EvruVNq5HlhWY2TOefL7wiknXYZByjqu1OD3EZfc130_assertion SIO_000772 15681302 NP90351.RAVX7EvruVNq5HlhWY2TOefL7wiknXYZByjqu1OD3EZfc130_provenance.
- NP90351.RAVX7EvruVNq5HlhWY2TOefL7wiknXYZByjqu1OD3EZfc130_assertion wasDerivedFrom gad-20150221 NP90351.RAVX7EvruVNq5HlhWY2TOefL7wiknXYZByjqu1OD3EZfc130_provenance.
- NP90351.RAVX7EvruVNq5HlhWY2TOefL7wiknXYZByjqu1OD3EZfc130_assertion wasGeneratedBy ECO_0000203 NP90351.RAVX7EvruVNq5HlhWY2TOefL7wiknXYZByjqu1OD3EZfc130_provenance.
- gad-20150221 importedOn "2015-02-21" NP90351.RAVX7EvruVNq5HlhWY2TOefL7wiknXYZByjqu1OD3EZfc130_provenance.