Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP757209.RAiRYb1QiGEYUpt6TJqxVxwveiZTT3KxwfKimm6w-uRDk130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP757209.RAiRYb1QiGEYUpt6TJqxVxwveiZTT3KxwfKimm6w-uRDk130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP757209.RAiRYb1QiGEYUpt6TJqxVxwveiZTT3KxwfKimm6w-uRDk130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP757209.RAiRYb1QiGEYUpt6TJqxVxwveiZTT3KxwfKimm6w-uRDk130_provenance.
- NP757209.RAiRYb1QiGEYUpt6TJqxVxwveiZTT3KxwfKimm6w-uRDk130_assertion description "[In order to shed some light on these inconsistent findings, a meta analysis was performed to clarify the role of G-403A polymorphism of RANTES gene in the susceptibility of CAD.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP757209.RAiRYb1QiGEYUpt6TJqxVxwveiZTT3KxwfKimm6w-uRDk130_provenance.
- NP757209.RAiRYb1QiGEYUpt6TJqxVxwveiZTT3KxwfKimm6w-uRDk130_assertion evidence source_evidence_literature NP757209.RAiRYb1QiGEYUpt6TJqxVxwveiZTT3KxwfKimm6w-uRDk130_provenance.
- NP757209.RAiRYb1QiGEYUpt6TJqxVxwveiZTT3KxwfKimm6w-uRDk130_assertion SIO_000772 23071760 NP757209.RAiRYb1QiGEYUpt6TJqxVxwveiZTT3KxwfKimm6w-uRDk130_provenance.
- NP757209.RAiRYb1QiGEYUpt6TJqxVxwveiZTT3KxwfKimm6w-uRDk130_assertion wasDerivedFrom befree-20140225 NP757209.RAiRYb1QiGEYUpt6TJqxVxwveiZTT3KxwfKimm6w-uRDk130_provenance.
- NP757209.RAiRYb1QiGEYUpt6TJqxVxwveiZTT3KxwfKimm6w-uRDk130_assertion wasGeneratedBy ECO_0000203 NP757209.RAiRYb1QiGEYUpt6TJqxVxwveiZTT3KxwfKimm6w-uRDk130_provenance.
- befree-20140225 importedOn "2014-02-25" NP757209.RAiRYb1QiGEYUpt6TJqxVxwveiZTT3KxwfKimm6w-uRDk130_provenance.