Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP777918.RApMLJj166sMpHb0vgQ8jfaiyST_VuCXdWIv2lKiHoQIo130_assertion> ?p ?o ?g. }
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- NP777918.RApMLJj166sMpHb0vgQ8jfaiyST_VuCXdWIv2lKiHoQIo130_assertion type Assertion NP777918.RApMLJj166sMpHb0vgQ8jfaiyST_VuCXdWIv2lKiHoQIo130_head.
- NP777918.RApMLJj166sMpHb0vgQ8jfaiyST_VuCXdWIv2lKiHoQIo130_assertion description "[Werner syndrome (WS) is a progeroid syndrome caused by autosomal recessive null mutations at the WRN locus.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP777918.RApMLJj166sMpHb0vgQ8jfaiyST_VuCXdWIv2lKiHoQIo130_provenance.
- NP777918.RApMLJj166sMpHb0vgQ8jfaiyST_VuCXdWIv2lKiHoQIo130_assertion evidence source_evidence_literature NP777918.RApMLJj166sMpHb0vgQ8jfaiyST_VuCXdWIv2lKiHoQIo130_provenance.
- NP777918.RApMLJj166sMpHb0vgQ8jfaiyST_VuCXdWIv2lKiHoQIo130_assertion SIO_000772 11186893 NP777918.RApMLJj166sMpHb0vgQ8jfaiyST_VuCXdWIv2lKiHoQIo130_provenance.
- NP777918.RApMLJj166sMpHb0vgQ8jfaiyST_VuCXdWIv2lKiHoQIo130_assertion wasDerivedFrom befree-20150227 NP777918.RApMLJj166sMpHb0vgQ8jfaiyST_VuCXdWIv2lKiHoQIo130_provenance.
- NP777918.RApMLJj166sMpHb0vgQ8jfaiyST_VuCXdWIv2lKiHoQIo130_assertion wasGeneratedBy ECO_0000203 NP777918.RApMLJj166sMpHb0vgQ8jfaiyST_VuCXdWIv2lKiHoQIo130_provenance.