Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP777918.RApMLJj166sMpHb0vgQ8jfaiyST_VuCXdWIv2lKiHoQIo130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP777918.RApMLJj166sMpHb0vgQ8jfaiyST_VuCXdWIv2lKiHoQIo130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP777918.RApMLJj166sMpHb0vgQ8jfaiyST_VuCXdWIv2lKiHoQIo130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP777918.RApMLJj166sMpHb0vgQ8jfaiyST_VuCXdWIv2lKiHoQIo130_provenance.
- 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.
- befree-20150227 importedOn "2015-02-27" NP777918.RApMLJj166sMpHb0vgQ8jfaiyST_VuCXdWIv2lKiHoQIo130_provenance.