Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP858467.RA1bhdFrgEPDLkhl1EtxDRNmoUZCtIWsyh-qfYaGcIunQ130_assertion> ?p ?o ?g. }
Showing items 1 to 6 of
6
with 100 items per page.
- NP858467.RA1bhdFrgEPDLkhl1EtxDRNmoUZCtIWsyh-qfYaGcIunQ130_assertion type Assertion NP858467.RA1bhdFrgEPDLkhl1EtxDRNmoUZCtIWsyh-qfYaGcIunQ130_head.
- NP858467.RA1bhdFrgEPDLkhl1EtxDRNmoUZCtIWsyh-qfYaGcIunQ130_assertion description "[Necdin deletion is associated with Prader-Willi syndrome.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP858467.RA1bhdFrgEPDLkhl1EtxDRNmoUZCtIWsyh-qfYaGcIunQ130_provenance.
- NP858467.RA1bhdFrgEPDLkhl1EtxDRNmoUZCtIWsyh-qfYaGcIunQ130_assertion evidence source_evidence_literature NP858467.RA1bhdFrgEPDLkhl1EtxDRNmoUZCtIWsyh-qfYaGcIunQ130_provenance.
- NP858467.RA1bhdFrgEPDLkhl1EtxDRNmoUZCtIWsyh-qfYaGcIunQ130_assertion SIO_000772 21150695 NP858467.RA1bhdFrgEPDLkhl1EtxDRNmoUZCtIWsyh-qfYaGcIunQ130_provenance.
- NP858467.RA1bhdFrgEPDLkhl1EtxDRNmoUZCtIWsyh-qfYaGcIunQ130_assertion wasDerivedFrom befree-2016 NP858467.RA1bhdFrgEPDLkhl1EtxDRNmoUZCtIWsyh-qfYaGcIunQ130_provenance.
- NP858467.RA1bhdFrgEPDLkhl1EtxDRNmoUZCtIWsyh-qfYaGcIunQ130_assertion wasGeneratedBy ECO_0000203 NP858467.RA1bhdFrgEPDLkhl1EtxDRNmoUZCtIWsyh-qfYaGcIunQ130_provenance.