Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP4606.RA0QKD24ZURlmrNeqnRYY15P7tGDtYhJHV3ndxQJuLGEg130_provenance>. }
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- source_evidence_curated type ECO_0000205 NP4606.RA0QKD24ZURlmrNeqnRYY15P7tGDtYhJHV3ndxQJuLGEg130_provenance.
- source_evidence_curated label "DisGeNET evidence - CURATED" NP4606.RA0QKD24ZURlmrNeqnRYY15P7tGDtYhJHV3ndxQJuLGEg130_provenance.
- source_evidence_curated comment "Gene-disease associations manually curated." NP4606.RA0QKD24ZURlmrNeqnRYY15P7tGDtYhJHV3ndxQJuLGEg130_provenance.
- NP4606.RA0QKD24ZURlmrNeqnRYY15P7tGDtYhJHV3ndxQJuLGEg130_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." NP4606.RA0QKD24ZURlmrNeqnRYY15P7tGDtYhJHV3ndxQJuLGEg130_provenance.
- NP4606.RA0QKD24ZURlmrNeqnRYY15P7tGDtYhJHV3ndxQJuLGEg130_assertion evidence source_evidence_curated NP4606.RA0QKD24ZURlmrNeqnRYY15P7tGDtYhJHV3ndxQJuLGEg130_provenance.
- NP4606.RA0QKD24ZURlmrNeqnRYY15P7tGDtYhJHV3ndxQJuLGEg130_assertion SIO_000772 20140240 NP4606.RA0QKD24ZURlmrNeqnRYY15P7tGDtYhJHV3ndxQJuLGEg130_provenance.
- NP4606.RA0QKD24ZURlmrNeqnRYY15P7tGDtYhJHV3ndxQJuLGEg130_assertion wasDerivedFrom uniprot-20150221 NP4606.RA0QKD24ZURlmrNeqnRYY15P7tGDtYhJHV3ndxQJuLGEg130_provenance.
- NP4606.RA0QKD24ZURlmrNeqnRYY15P7tGDtYhJHV3ndxQJuLGEg130_assertion wasGeneratedBy ECO_0000218 NP4606.RA0QKD24ZURlmrNeqnRYY15P7tGDtYhJHV3ndxQJuLGEg130_provenance.
- uniprot-20150221 importedOn "2015-02-21" NP4606.RA0QKD24ZURlmrNeqnRYY15P7tGDtYhJHV3ndxQJuLGEg130_provenance.