Matches in Nanopublications for { <http://rdf.disgenet.org/nanopublications.trig#NP29830.RA_K_ckx1s1mfq3Mv0BoOsSFZIQGeAWGXOme45-8r1M6w130_assertion> ?p ?o ?g. }
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- NP29830.RA_K_ckx1s1mfq3Mv0BoOsSFZIQGeAWGXOme45-8r1M6w130_assertion type Assertion NP29830.RA_K_ckx1s1mfq3Mv0BoOsSFZIQGeAWGXOme45-8r1M6w130_head.
- NP29830.RA_K_ckx1s1mfq3Mv0BoOsSFZIQGeAWGXOme45-8r1M6w130_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." NP29830.RA_K_ckx1s1mfq3Mv0BoOsSFZIQGeAWGXOme45-8r1M6w130_provenance.
- NP29830.RA_K_ckx1s1mfq3Mv0BoOsSFZIQGeAWGXOme45-8r1M6w130_assertion evidence source_evidence_curated NP29830.RA_K_ckx1s1mfq3Mv0BoOsSFZIQGeAWGXOme45-8r1M6w130_provenance.
- NP29830.RA_K_ckx1s1mfq3Mv0BoOsSFZIQGeAWGXOme45-8r1M6w130_assertion SIO_000772 20140240 NP29830.RA_K_ckx1s1mfq3Mv0BoOsSFZIQGeAWGXOme45-8r1M6w130_provenance.
- NP29830.RA_K_ckx1s1mfq3Mv0BoOsSFZIQGeAWGXOme45-8r1M6w130_assertion wasDerivedFrom ctd_human-20130708 NP29830.RA_K_ckx1s1mfq3Mv0BoOsSFZIQGeAWGXOme45-8r1M6w130_provenance.
- NP29830.RA_K_ckx1s1mfq3Mv0BoOsSFZIQGeAWGXOme45-8r1M6w130_assertion wasGeneratedBy ECO_0000218 NP29830.RA_K_ckx1s1mfq3Mv0BoOsSFZIQGeAWGXOme45-8r1M6w130_provenance.