Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP222399.RAykA-Mt2Ky-XDEyUV9VKy9-dYAqOvy3wyoR5nwekAlJg130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP222399.RAykA-Mt2Ky-XDEyUV9VKy9-dYAqOvy3wyoR5nwekAlJg130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP222399.RAykA-Mt2Ky-XDEyUV9VKy9-dYAqOvy3wyoR5nwekAlJg130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP222399.RAykA-Mt2Ky-XDEyUV9VKy9-dYAqOvy3wyoR5nwekAlJg130_provenance.
- NP222399.RAykA-Mt2Ky-XDEyUV9VKy9-dYAqOvy3wyoR5nwekAlJg130_assertion description "[a possibly inactivating mutation in the SNRPN minimal promoter region was identified in Prader-Willi syndrome ]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP222399.RAykA-Mt2Ky-XDEyUV9VKy9-dYAqOvy3wyoR5nwekAlJg130_provenance.
- NP222399.RAykA-Mt2Ky-XDEyUV9VKy9-dYAqOvy3wyoR5nwekAlJg130_assertion evidence source_evidence_literature NP222399.RAykA-Mt2Ky-XDEyUV9VKy9-dYAqOvy3wyoR5nwekAlJg130_provenance.
- NP222399.RAykA-Mt2Ky-XDEyUV9VKy9-dYAqOvy3wyoR5nwekAlJg130_assertion SIO_000772 17262171 NP222399.RAykA-Mt2Ky-XDEyUV9VKy9-dYAqOvy3wyoR5nwekAlJg130_provenance.
- NP222399.RAykA-Mt2Ky-XDEyUV9VKy9-dYAqOvy3wyoR5nwekAlJg130_assertion wasDerivedFrom lhgdn-20090331 NP222399.RAykA-Mt2Ky-XDEyUV9VKy9-dYAqOvy3wyoR5nwekAlJg130_provenance.
- NP222399.RAykA-Mt2Ky-XDEyUV9VKy9-dYAqOvy3wyoR5nwekAlJg130_assertion wasGeneratedBy ECO_0000203 NP222399.RAykA-Mt2Ky-XDEyUV9VKy9-dYAqOvy3wyoR5nwekAlJg130_provenance.
- lhgdn-20090331 importedOn "2009-03-31" NP222399.RAykA-Mt2Ky-XDEyUV9VKy9-dYAqOvy3wyoR5nwekAlJg130_provenance.