Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP504115.RAwhQOx1KeBqrtCRhCiFZKJC1JrlqNqzCpI7SFviE35Rw130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP504115.RAwhQOx1KeBqrtCRhCiFZKJC1JrlqNqzCpI7SFviE35Rw130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP504115.RAwhQOx1KeBqrtCRhCiFZKJC1JrlqNqzCpI7SFviE35Rw130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP504115.RAwhQOx1KeBqrtCRhCiFZKJC1JrlqNqzCpI7SFviE35Rw130_provenance.
- NP504115.RAwhQOx1KeBqrtCRhCiFZKJC1JrlqNqzCpI7SFviE35Rw130_assertion description "[Investigating all common variants in IL1A, IL1B, IL1RN,IL6 and IL10 genes revealed a statistically significant association (rs452204 p(empirical) = 0.02) with one IL1RN variant and ESRD.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP504115.RAwhQOx1KeBqrtCRhCiFZKJC1JrlqNqzCpI7SFviE35Rw130_provenance.
- NP504115.RAwhQOx1KeBqrtCRhCiFZKJC1JrlqNqzCpI7SFviE35Rw130_assertion evidence source_evidence_literature NP504115.RAwhQOx1KeBqrtCRhCiFZKJC1JrlqNqzCpI7SFviE35Rw130_provenance.
- NP504115.RAwhQOx1KeBqrtCRhCiFZKJC1JrlqNqzCpI7SFviE35Rw130_assertion SIO_000772 20551628 NP504115.RAwhQOx1KeBqrtCRhCiFZKJC1JrlqNqzCpI7SFviE35Rw130_provenance.
- NP504115.RAwhQOx1KeBqrtCRhCiFZKJC1JrlqNqzCpI7SFviE35Rw130_assertion wasDerivedFrom befree-20150227 NP504115.RAwhQOx1KeBqrtCRhCiFZKJC1JrlqNqzCpI7SFviE35Rw130_provenance.
- NP504115.RAwhQOx1KeBqrtCRhCiFZKJC1JrlqNqzCpI7SFviE35Rw130_assertion wasGeneratedBy ECO_0000203 NP504115.RAwhQOx1KeBqrtCRhCiFZKJC1JrlqNqzCpI7SFviE35Rw130_provenance.
- befree-20150227 importedOn "2015-02-27" NP504115.RAwhQOx1KeBqrtCRhCiFZKJC1JrlqNqzCpI7SFviE35Rw130_provenance.