Matches in Nanopublications for { <http://rdf.disgenet.org/nanopublications.trig#NP29834.RAIJcwXYz0ShNuP-vLHdjKCLL4IQwaX730yraMhVLEAVE130_assertion> ?p ?o ?g. }
Showing items 1 to 6 of
6
with 100 items per page.
- NP29834.RAIJcwXYz0ShNuP-vLHdjKCLL4IQwaX730yraMhVLEAVE130_assertion type Assertion NP29834.RAIJcwXYz0ShNuP-vLHdjKCLL4IQwaX730yraMhVLEAVE130_head.
- NP29834.RAIJcwXYz0ShNuP-vLHdjKCLL4IQwaX730yraMhVLEAVE130_assertion description "[Mutations in SLC29A3, encoding an equilibrative nucleoside transporter ENT3, cause a familial histiocytosis syndrome (Faisalabad histiocytosis) and familial Rosai-Dorfman disease.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP29834.RAIJcwXYz0ShNuP-vLHdjKCLL4IQwaX730yraMhVLEAVE130_provenance.
- NP29834.RAIJcwXYz0ShNuP-vLHdjKCLL4IQwaX730yraMhVLEAVE130_assertion evidence source_evidence_curated NP29834.RAIJcwXYz0ShNuP-vLHdjKCLL4IQwaX730yraMhVLEAVE130_provenance.
- NP29834.RAIJcwXYz0ShNuP-vLHdjKCLL4IQwaX730yraMhVLEAVE130_assertion SIO_000772 20140240 NP29834.RAIJcwXYz0ShNuP-vLHdjKCLL4IQwaX730yraMhVLEAVE130_provenance.
- NP29834.RAIJcwXYz0ShNuP-vLHdjKCLL4IQwaX730yraMhVLEAVE130_assertion wasDerivedFrom ctd_human-20130708 NP29834.RAIJcwXYz0ShNuP-vLHdjKCLL4IQwaX730yraMhVLEAVE130_provenance.
- NP29834.RAIJcwXYz0ShNuP-vLHdjKCLL4IQwaX730yraMhVLEAVE130_assertion wasGeneratedBy ECO_0000218 NP29834.RAIJcwXYz0ShNuP-vLHdjKCLL4IQwaX730yraMhVLEAVE130_provenance.