Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP204158.RACRS9EaTVOTGSgwM_WCQZvmSOV9ePq66YBOgFCnHwRGc130_assertion> ?p ?o ?g. }
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- NP204158.RACRS9EaTVOTGSgwM_WCQZvmSOV9ePq66YBOgFCnHwRGc130_assertion type Assertion NP204158.RACRS9EaTVOTGSgwM_WCQZvmSOV9ePq66YBOgFCnHwRGc130_head.
- 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.
- NP204158.RACRS9EaTVOTGSgwM_WCQZvmSOV9ePq66YBOgFCnHwRGc130_assertion evidence source_evidence_literature NP204158.RACRS9EaTVOTGSgwM_WCQZvmSOV9ePq66YBOgFCnHwRGc130_provenance.
- NP204158.RACRS9EaTVOTGSgwM_WCQZvmSOV9ePq66YBOgFCnHwRGc130_assertion SIO_000772 11749051 NP204158.RACRS9EaTVOTGSgwM_WCQZvmSOV9ePq66YBOgFCnHwRGc130_provenance.
- NP204158.RACRS9EaTVOTGSgwM_WCQZvmSOV9ePq66YBOgFCnHwRGc130_assertion wasDerivedFrom lhgdn-20090331 NP204158.RACRS9EaTVOTGSgwM_WCQZvmSOV9ePq66YBOgFCnHwRGc130_provenance.
- NP204158.RACRS9EaTVOTGSgwM_WCQZvmSOV9ePq66YBOgFCnHwRGc130_assertion wasGeneratedBy ECO_0000203 NP204158.RACRS9EaTVOTGSgwM_WCQZvmSOV9ePq66YBOgFCnHwRGc130_provenance.