Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP204158.RACRS9EaTVOTGSgwM_WCQZvmSOV9ePq66YBOgFCnHwRGc130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP204158.RACRS9EaTVOTGSgwM_WCQZvmSOV9ePq66YBOgFCnHwRGc130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP204158.RACRS9EaTVOTGSgwM_WCQZvmSOV9ePq66YBOgFCnHwRGc130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP204158.RACRS9EaTVOTGSgwM_WCQZvmSOV9ePq66YBOgFCnHwRGc130_provenance.
- lhgdn-20090331 importedOn "2009-03-31" NP204158.RACRS9EaTVOTGSgwM_WCQZvmSOV9ePq66YBOgFCnHwRGc130_provenance.
- NP204158.RACRS9EaTVOTGSgwM_WCQZvmSOV9ePq66YBOgFCnHwRGc130_assertion wasGeneratedBy ECO_0000203 NP204158.RACRS9EaTVOTGSgwM_WCQZvmSOV9ePq66YBOgFCnHwRGc130_provenance.
- NP204158.RACRS9EaTVOTGSgwM_WCQZvmSOV9ePq66YBOgFCnHwRGc130_assertion wasDerivedFrom lhgdn-20090331 NP204158.RACRS9EaTVOTGSgwM_WCQZvmSOV9ePq66YBOgFCnHwRGc130_provenance.
- NP204158.RACRS9EaTVOTGSgwM_WCQZvmSOV9ePq66YBOgFCnHwRGc130_assertion SIO_000772 11749051 NP204158.RACRS9EaTVOTGSgwM_WCQZvmSOV9ePq66YBOgFCnHwRGc130_provenance.
- NP204158.RACRS9EaTVOTGSgwM_WCQZvmSOV9ePq66YBOgFCnHwRGc130_assertion evidence source_evidence_literature NP204158.RACRS9EaTVOTGSgwM_WCQZvmSOV9ePq66YBOgFCnHwRGc130_provenance.
- NP204158.RACRS9EaTVOTGSgwM_WCQZvmSOV9ePq66YBOgFCnHwRGc130_assertion description "[Suggested as a candidate gene for a dominant syndrome that consists of inclusion body myopathy, Paget disease of bone, and dementia.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP204158.RACRS9EaTVOTGSgwM_WCQZvmSOV9ePq66YBOgFCnHwRGc130_provenance.