Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP8832.RAuVSqNnWdBrbiIa60nMGU6A19MHdySAv4M4GrvnCIkQs130_provenance>. }
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- source_evidence_curated type ECO_0000205 NP8832.RAuVSqNnWdBrbiIa60nMGU6A19MHdySAv4M4GrvnCIkQs130_provenance.
- source_evidence_curated label "DisGeNET evidence - CURATED" NP8832.RAuVSqNnWdBrbiIa60nMGU6A19MHdySAv4M4GrvnCIkQs130_provenance.
- source_evidence_curated comment "Gene-disease associations manually curated." NP8832.RAuVSqNnWdBrbiIa60nMGU6A19MHdySAv4M4GrvnCIkQs130_provenance.
- NP8832.RAuVSqNnWdBrbiIa60nMGU6A19MHdySAv4M4GrvnCIkQs130_assertion description "[Autosomal recessive chronic granulomatous disease with absence of the 67-kD cytosolic NADPH oxidase component: identification of mutation and detection of carriers.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP8832.RAuVSqNnWdBrbiIa60nMGU6A19MHdySAv4M4GrvnCIkQs130_provenance.
- NP8832.RAuVSqNnWdBrbiIa60nMGU6A19MHdySAv4M4GrvnCIkQs130_assertion evidence source_evidence_curated NP8832.RAuVSqNnWdBrbiIa60nMGU6A19MHdySAv4M4GrvnCIkQs130_provenance.
- NP8832.RAuVSqNnWdBrbiIa60nMGU6A19MHdySAv4M4GrvnCIkQs130_assertion SIO_000772 8286749 NP8832.RAuVSqNnWdBrbiIa60nMGU6A19MHdySAv4M4GrvnCIkQs130_provenance.
- NP8832.RAuVSqNnWdBrbiIa60nMGU6A19MHdySAv4M4GrvnCIkQs130_assertion wasDerivedFrom uniprot-2016 NP8832.RAuVSqNnWdBrbiIa60nMGU6A19MHdySAv4M4GrvnCIkQs130_provenance.
- NP8832.RAuVSqNnWdBrbiIa60nMGU6A19MHdySAv4M4GrvnCIkQs130_assertion wasGeneratedBy ECO_0000218 NP8832.RAuVSqNnWdBrbiIa60nMGU6A19MHdySAv4M4GrvnCIkQs130_provenance.
- uniprot-2016 importedOn "2016-01-25" NP8832.RAuVSqNnWdBrbiIa60nMGU6A19MHdySAv4M4GrvnCIkQs130_provenance.