Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP76363.RAl_Wfj4L0uWQR7Y70LFW3FKZUqV9oZR79YpeVOWmxGq8130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP76363.RAl_Wfj4L0uWQR7Y70LFW3FKZUqV9oZR79YpeVOWmxGq8130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP76363.RAl_Wfj4L0uWQR7Y70LFW3FKZUqV9oZR79YpeVOWmxGq8130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP76363.RAl_Wfj4L0uWQR7Y70LFW3FKZUqV9oZR79YpeVOWmxGq8130_provenance.
- NP76363.RAl_Wfj4L0uWQR7Y70LFW3FKZUqV9oZR79YpeVOWmxGq8130_assertion description "[XRCC1 and XRCC3 variants and risk of glioma and meningioma.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP76363.RAl_Wfj4L0uWQR7Y70LFW3FKZUqV9oZR79YpeVOWmxGq8130_provenance.
- NP76363.RAl_Wfj4L0uWQR7Y70LFW3FKZUqV9oZR79YpeVOWmxGq8130_assertion evidence source_evidence_literature NP76363.RAl_Wfj4L0uWQR7Y70LFW3FKZUqV9oZR79YpeVOWmxGq8130_provenance.
- NP76363.RAl_Wfj4L0uWQR7Y70LFW3FKZUqV9oZR79YpeVOWmxGq8130_assertion SIO_000772 18330515 NP76363.RAl_Wfj4L0uWQR7Y70LFW3FKZUqV9oZR79YpeVOWmxGq8130_provenance.
- NP76363.RAl_Wfj4L0uWQR7Y70LFW3FKZUqV9oZR79YpeVOWmxGq8130_assertion wasDerivedFrom gad-20150221 NP76363.RAl_Wfj4L0uWQR7Y70LFW3FKZUqV9oZR79YpeVOWmxGq8130_provenance.
- NP76363.RAl_Wfj4L0uWQR7Y70LFW3FKZUqV9oZR79YpeVOWmxGq8130_assertion wasGeneratedBy ECO_0000203 NP76363.RAl_Wfj4L0uWQR7Y70LFW3FKZUqV9oZR79YpeVOWmxGq8130_provenance.
- gad-20150221 importedOn "2015-02-21" NP76363.RAl_Wfj4L0uWQR7Y70LFW3FKZUqV9oZR79YpeVOWmxGq8130_provenance.