Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP769525.RALGdckgQPs33KFbK4WxPa8a9R2jXjVirQq4g-Efz0TqA130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP769525.RALGdckgQPs33KFbK4WxPa8a9R2jXjVirQq4g-Efz0TqA130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP769525.RALGdckgQPs33KFbK4WxPa8a9R2jXjVirQq4g-Efz0TqA130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP769525.RALGdckgQPs33KFbK4WxPa8a9R2jXjVirQq4g-Efz0TqA130_provenance.
- NP769525.RALGdckgQPs33KFbK4WxPa8a9R2jXjVirQq4g-Efz0TqA130_assertion description "[These data indicate that carriage of the less frequent allele of the Taq I RFLP (t) in the VDR gene significantly increases the risk of developing L-EOP.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP769525.RALGdckgQPs33KFbK4WxPa8a9R2jXjVirQq4g-Efz0TqA130_provenance.
- NP769525.RALGdckgQPs33KFbK4WxPa8a9R2jXjVirQq4g-Efz0TqA130_assertion evidence source_evidence_literature NP769525.RALGdckgQPs33KFbK4WxPa8a9R2jXjVirQq4g-Efz0TqA130_provenance.
- NP769525.RALGdckgQPs33KFbK4WxPa8a9R2jXjVirQq4g-Efz0TqA130_assertion SIO_000772 10505806 NP769525.RALGdckgQPs33KFbK4WxPa8a9R2jXjVirQq4g-Efz0TqA130_provenance.
- NP769525.RALGdckgQPs33KFbK4WxPa8a9R2jXjVirQq4g-Efz0TqA130_assertion wasDerivedFrom befree-20150227 NP769525.RALGdckgQPs33KFbK4WxPa8a9R2jXjVirQq4g-Efz0TqA130_provenance.
- NP769525.RALGdckgQPs33KFbK4WxPa8a9R2jXjVirQq4g-Efz0TqA130_assertion wasGeneratedBy ECO_0000203 NP769525.RALGdckgQPs33KFbK4WxPa8a9R2jXjVirQq4g-Efz0TqA130_provenance.
- befree-20150227 importedOn "2015-02-27" NP769525.RALGdckgQPs33KFbK4WxPa8a9R2jXjVirQq4g-Efz0TqA130_provenance.