Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP488921.RAegpkM4zq4FYC_lWgwjki0P7FRjpUVZu88UEcXbCDWSs130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP488921.RAegpkM4zq4FYC_lWgwjki0P7FRjpUVZu88UEcXbCDWSs130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP488921.RAegpkM4zq4FYC_lWgwjki0P7FRjpUVZu88UEcXbCDWSs130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP488921.RAegpkM4zq4FYC_lWgwjki0P7FRjpUVZu88UEcXbCDWSs130_provenance.
- NP488921.RAegpkM4zq4FYC_lWgwjki0P7FRjpUVZu88UEcXbCDWSs130_assertion description "[When the simple FS patients were divided into two groups according to either having (familial) or not having a family history of FS in close relatives (sporadic), there was a significant association between IL1B -511 SNP and sporadic simple FS (p=0.003).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP488921.RAegpkM4zq4FYC_lWgwjki0P7FRjpUVZu88UEcXbCDWSs130_provenance.
- NP488921.RAegpkM4zq4FYC_lWgwjki0P7FRjpUVZu88UEcXbCDWSs130_assertion evidence source_evidence_literature NP488921.RAegpkM4zq4FYC_lWgwjki0P7FRjpUVZu88UEcXbCDWSs130_provenance.
- NP488921.RAegpkM4zq4FYC_lWgwjki0P7FRjpUVZu88UEcXbCDWSs130_assertion SIO_000772 19854014 NP488921.RAegpkM4zq4FYC_lWgwjki0P7FRjpUVZu88UEcXbCDWSs130_provenance.
- NP488921.RAegpkM4zq4FYC_lWgwjki0P7FRjpUVZu88UEcXbCDWSs130_assertion wasDerivedFrom befree-20150227 NP488921.RAegpkM4zq4FYC_lWgwjki0P7FRjpUVZu88UEcXbCDWSs130_provenance.
- NP488921.RAegpkM4zq4FYC_lWgwjki0P7FRjpUVZu88UEcXbCDWSs130_assertion wasGeneratedBy ECO_0000203 NP488921.RAegpkM4zq4FYC_lWgwjki0P7FRjpUVZu88UEcXbCDWSs130_provenance.
- befree-20150227 importedOn "2015-02-27" NP488921.RAegpkM4zq4FYC_lWgwjki0P7FRjpUVZu88UEcXbCDWSs130_provenance.