Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP25641.RAx4zzgXXFauAh-m3Tv9KAZyY2kd0IWK2JifUxXjwSVPA130_assertion> ?p ?o ?g. }
Showing items 1 to 6 of
6
with 100 items per page.
- NP25641.RAx4zzgXXFauAh-m3Tv9KAZyY2kd0IWK2JifUxXjwSVPA130_assertion type Assertion NP25641.RAx4zzgXXFauAh-m3Tv9KAZyY2kd0IWK2JifUxXjwSVPA130_head.
- NP25641.RAx4zzgXXFauAh-m3Tv9KAZyY2kd0IWK2JifUxXjwSVPA130_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." NP25641.RAx4zzgXXFauAh-m3Tv9KAZyY2kd0IWK2JifUxXjwSVPA130_provenance.
- NP25641.RAx4zzgXXFauAh-m3Tv9KAZyY2kd0IWK2JifUxXjwSVPA130_assertion evidence source_evidence_curated NP25641.RAx4zzgXXFauAh-m3Tv9KAZyY2kd0IWK2JifUxXjwSVPA130_provenance.
- NP25641.RAx4zzgXXFauAh-m3Tv9KAZyY2kd0IWK2JifUxXjwSVPA130_assertion SIO_000772 20140240 NP25641.RAx4zzgXXFauAh-m3Tv9KAZyY2kd0IWK2JifUxXjwSVPA130_provenance.
- NP25641.RAx4zzgXXFauAh-m3Tv9KAZyY2kd0IWK2JifUxXjwSVPA130_assertion wasDerivedFrom ctd_human-2016 NP25641.RAx4zzgXXFauAh-m3Tv9KAZyY2kd0IWK2JifUxXjwSVPA130_provenance.
- NP25641.RAx4zzgXXFauAh-m3Tv9KAZyY2kd0IWK2JifUxXjwSVPA130_assertion wasGeneratedBy ECO_0000218 NP25641.RAx4zzgXXFauAh-m3Tv9KAZyY2kd0IWK2JifUxXjwSVPA130_provenance.