Matches in Nanopublications for { ?s ?p "[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."@en ?g. }
Showing items 1 to 2 of
2
with 100 items per page.
- 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.
- NP307697.RAHKvn4fxYQJovSQcqyM3oyuRVklcmGxDV0Zbe1VK21d8130_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." NP307697.RAHKvn4fxYQJovSQcqyM3oyuRVklcmGxDV0Zbe1VK21d8130_provenance.