Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP487997.RAinkNz8TViP_-JFhOj5cMnO2PGZkddJU43RYCf3lxaAY130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP487997.RAinkNz8TViP_-JFhOj5cMnO2PGZkddJU43RYCf3lxaAY130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP487997.RAinkNz8TViP_-JFhOj5cMnO2PGZkddJU43RYCf3lxaAY130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP487997.RAinkNz8TViP_-JFhOj5cMnO2PGZkddJU43RYCf3lxaAY130_provenance.
- NP487997.RAinkNz8TViP_-JFhOj5cMnO2PGZkddJU43RYCf3lxaAY130_assertion description "[We studied genetic polymorphisms in the promoter region at position -511 of the interleukin (IL) -1beta gene (IL-1B-511) and at position -889 of the IL-1alpha gene (IL-1A-889), in 111 Japanese patients with multiple system atrophy (MSA) and 160 controls.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP487997.RAinkNz8TViP_-JFhOj5cMnO2PGZkddJU43RYCf3lxaAY130_provenance.
- NP487997.RAinkNz8TViP_-JFhOj5cMnO2PGZkddJU43RYCf3lxaAY130_assertion evidence source_evidence_literature NP487997.RAinkNz8TViP_-JFhOj5cMnO2PGZkddJU43RYCf3lxaAY130_provenance.
- NP487997.RAinkNz8TViP_-JFhOj5cMnO2PGZkddJU43RYCf3lxaAY130_assertion SIO_000772 12210881 NP487997.RAinkNz8TViP_-JFhOj5cMnO2PGZkddJU43RYCf3lxaAY130_provenance.
- NP487997.RAinkNz8TViP_-JFhOj5cMnO2PGZkddJU43RYCf3lxaAY130_assertion wasDerivedFrom befree-20150227 NP487997.RAinkNz8TViP_-JFhOj5cMnO2PGZkddJU43RYCf3lxaAY130_provenance.
- NP487997.RAinkNz8TViP_-JFhOj5cMnO2PGZkddJU43RYCf3lxaAY130_assertion wasGeneratedBy ECO_0000203 NP487997.RAinkNz8TViP_-JFhOj5cMnO2PGZkddJU43RYCf3lxaAY130_provenance.
- befree-20150227 importedOn "2015-02-27" NP487997.RAinkNz8TViP_-JFhOj5cMnO2PGZkddJU43RYCf3lxaAY130_provenance.