Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP8778.RA-pDEfKxjd8jQfadiqmMMM4jY83Z4t2TwsbeQhisw75k130_provenance>. }
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- source_evidence_curated type ECO_0000205 NP8778.RA-pDEfKxjd8jQfadiqmMMM4jY83Z4t2TwsbeQhisw75k130_provenance.
- source_evidence_curated label "DisGeNET evidence - CURATED" NP8778.RA-pDEfKxjd8jQfadiqmMMM4jY83Z4t2TwsbeQhisw75k130_provenance.
- source_evidence_curated comment "Gene-disease associations manually curated." NP8778.RA-pDEfKxjd8jQfadiqmMMM4jY83Z4t2TwsbeQhisw75k130_provenance.
- NP8778.RA-pDEfKxjd8jQfadiqmMMM4jY83Z4t2TwsbeQhisw75k130_assertion description "[Identification of allele-specific p22-phox mutations in a compound heterozygous patient with chronic granulomatous disease by mismatch PCR and restriction enzyme analysis.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP8778.RA-pDEfKxjd8jQfadiqmMMM4jY83Z4t2TwsbeQhisw75k130_provenance.
- NP8778.RA-pDEfKxjd8jQfadiqmMMM4jY83Z4t2TwsbeQhisw75k130_assertion evidence source_evidence_curated NP8778.RA-pDEfKxjd8jQfadiqmMMM4jY83Z4t2TwsbeQhisw75k130_provenance.
- NP8778.RA-pDEfKxjd8jQfadiqmMMM4jY83Z4t2TwsbeQhisw75k130_assertion SIO_000772 8168815 NP8778.RA-pDEfKxjd8jQfadiqmMMM4jY83Z4t2TwsbeQhisw75k130_provenance.
- NP8778.RA-pDEfKxjd8jQfadiqmMMM4jY83Z4t2TwsbeQhisw75k130_assertion wasDerivedFrom uniprot-2016 NP8778.RA-pDEfKxjd8jQfadiqmMMM4jY83Z4t2TwsbeQhisw75k130_provenance.
- NP8778.RA-pDEfKxjd8jQfadiqmMMM4jY83Z4t2TwsbeQhisw75k130_assertion wasGeneratedBy ECO_0000218 NP8778.RA-pDEfKxjd8jQfadiqmMMM4jY83Z4t2TwsbeQhisw75k130_provenance.
- uniprot-2016 importedOn "2016-01-25" NP8778.RA-pDEfKxjd8jQfadiqmMMM4jY83Z4t2TwsbeQhisw75k130_provenance.