Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP787168.RAMQCT1K-AgTMDL95C41711VFscnwMB5EsVLfD6hSCOA4130_assertion> ?p ?o ?g. }
Showing items 1 to 6 of
6
with 100 items per page.
- NP787168.RAMQCT1K-AgTMDL95C41711VFscnwMB5EsVLfD6hSCOA4130_assertion type Assertion NP787168.RAMQCT1K-AgTMDL95C41711VFscnwMB5EsVLfD6hSCOA4130_head.
- NP787168.RAMQCT1K-AgTMDL95C41711VFscnwMB5EsVLfD6hSCOA4130_assertion wasGeneratedBy ECO_0000203 NP787168.RAMQCT1K-AgTMDL95C41711VFscnwMB5EsVLfD6hSCOA4130_provenance.
- NP787168.RAMQCT1K-AgTMDL95C41711VFscnwMB5EsVLfD6hSCOA4130_assertion wasDerivedFrom befree-2016 NP787168.RAMQCT1K-AgTMDL95C41711VFscnwMB5EsVLfD6hSCOA4130_provenance.
- NP787168.RAMQCT1K-AgTMDL95C41711VFscnwMB5EsVLfD6hSCOA4130_assertion SIO_000772 20075015 NP787168.RAMQCT1K-AgTMDL95C41711VFscnwMB5EsVLfD6hSCOA4130_provenance.
- NP787168.RAMQCT1K-AgTMDL95C41711VFscnwMB5EsVLfD6hSCOA4130_assertion evidence source_evidence_literature NP787168.RAMQCT1K-AgTMDL95C41711VFscnwMB5EsVLfD6hSCOA4130_provenance.
- NP787168.RAMQCT1K-AgTMDL95C41711VFscnwMB5EsVLfD6hSCOA4130_assertion description "[Mutations in the WRN gene are the causative factor of Werner syndrome (WS).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP787168.RAMQCT1K-AgTMDL95C41711VFscnwMB5EsVLfD6hSCOA4130_provenance.