Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP5084.RAvufW9MxndY_h6bEltcrphnNMcSv0XKRDZQSk57rMf2w130_provenance>. }
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- source_evidence_curated type ECO_0000205 NP5084.RAvufW9MxndY_h6bEltcrphnNMcSv0XKRDZQSk57rMf2w130_provenance.
- source_evidence_curated label "DisGeNET evidence - CURATED" NP5084.RAvufW9MxndY_h6bEltcrphnNMcSv0XKRDZQSk57rMf2w130_provenance.
- source_evidence_curated comment "Gene-disease associations manually curated." NP5084.RAvufW9MxndY_h6bEltcrphnNMcSv0XKRDZQSk57rMf2w130_provenance.
- NP5084.RAvufW9MxndY_h6bEltcrphnNMcSv0XKRDZQSk57rMf2w130_assertion description "[A human purine nucleoside phosphorylase deficiency caused by a single base change.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP5084.RAvufW9MxndY_h6bEltcrphnNMcSv0XKRDZQSk57rMf2w130_provenance.
- NP5084.RAvufW9MxndY_h6bEltcrphnNMcSv0XKRDZQSk57rMf2w130_assertion evidence source_evidence_curated NP5084.RAvufW9MxndY_h6bEltcrphnNMcSv0XKRDZQSk57rMf2w130_provenance.
- NP5084.RAvufW9MxndY_h6bEltcrphnNMcSv0XKRDZQSk57rMf2w130_assertion SIO_000772 3029074 NP5084.RAvufW9MxndY_h6bEltcrphnNMcSv0XKRDZQSk57rMf2w130_provenance.
- NP5084.RAvufW9MxndY_h6bEltcrphnNMcSv0XKRDZQSk57rMf2w130_assertion wasDerivedFrom uniprot-20130724 NP5084.RAvufW9MxndY_h6bEltcrphnNMcSv0XKRDZQSk57rMf2w130_provenance.
- NP5084.RAvufW9MxndY_h6bEltcrphnNMcSv0XKRDZQSk57rMf2w130_assertion wasGeneratedBy ECO_0000218 NP5084.RAvufW9MxndY_h6bEltcrphnNMcSv0XKRDZQSk57rMf2w130_provenance.
- uniprot-20130724 importedOn "2013-07-24" NP5084.RAvufW9MxndY_h6bEltcrphnNMcSv0XKRDZQSk57rMf2w130_provenance.