Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP174122.RAdfVy_ecHhtfhJRDNxmlzzzB8-M0VN-EkGS67UqarjVk130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP174122.RAdfVy_ecHhtfhJRDNxmlzzzB8-M0VN-EkGS67UqarjVk130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP174122.RAdfVy_ecHhtfhJRDNxmlzzzB8-M0VN-EkGS67UqarjVk130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP174122.RAdfVy_ecHhtfhJRDNxmlzzzB8-M0VN-EkGS67UqarjVk130_provenance.
- gad-20150221 importedOn "2015-02-21" NP174122.RAdfVy_ecHhtfhJRDNxmlzzzB8-M0VN-EkGS67UqarjVk130_provenance.
- NP174122.RAdfVy_ecHhtfhJRDNxmlzzzB8-M0VN-EkGS67UqarjVk130_assertion wasGeneratedBy ECO_0000203 NP174122.RAdfVy_ecHhtfhJRDNxmlzzzB8-M0VN-EkGS67UqarjVk130_provenance.
- NP174122.RAdfVy_ecHhtfhJRDNxmlzzzB8-M0VN-EkGS67UqarjVk130_assertion wasDerivedFrom gad-20150221 NP174122.RAdfVy_ecHhtfhJRDNxmlzzzB8-M0VN-EkGS67UqarjVk130_provenance.
- NP174122.RAdfVy_ecHhtfhJRDNxmlzzzB8-M0VN-EkGS67UqarjVk130_assertion SIO_000772 20436471 NP174122.RAdfVy_ecHhtfhJRDNxmlzzzB8-M0VN-EkGS67UqarjVk130_provenance.
- NP174122.RAdfVy_ecHhtfhJRDNxmlzzzB8-M0VN-EkGS67UqarjVk130_assertion evidence source_evidence_literature NP174122.RAdfVy_ecHhtfhJRDNxmlzzzB8-M0VN-EkGS67UqarjVk130_provenance.
- NP174122.RAdfVy_ecHhtfhJRDNxmlzzzB8-M0VN-EkGS67UqarjVk130_assertion description "[Genome-wide association study identifies variants at CSF1, OPTN and TNFRSF11A as genetic risk factors for Paget's disease of bone.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP174122.RAdfVy_ecHhtfhJRDNxmlzzzB8-M0VN-EkGS67UqarjVk130_provenance.