Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP1599.RAOh-01iWApcoFZXVASC4YgMRRXIb4DOIKUyLyapw0b7s130_provenance>. }
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- source_evidence_curated type ECO_0000205 NP1599.RAOh-01iWApcoFZXVASC4YgMRRXIb4DOIKUyLyapw0b7s130_provenance.
- source_evidence_curated label "DisGeNET evidence - CURATED" NP1599.RAOh-01iWApcoFZXVASC4YgMRRXIb4DOIKUyLyapw0b7s130_provenance.
- source_evidence_curated comment "Gene-disease associations manually curated." NP1599.RAOh-01iWApcoFZXVASC4YgMRRXIb4DOIKUyLyapw0b7s130_provenance.
- NP1599.RAOh-01iWApcoFZXVASC4YgMRRXIb4DOIKUyLyapw0b7s130_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." NP1599.RAOh-01iWApcoFZXVASC4YgMRRXIb4DOIKUyLyapw0b7s130_provenance.
- NP1599.RAOh-01iWApcoFZXVASC4YgMRRXIb4DOIKUyLyapw0b7s130_assertion evidence source_evidence_curated NP1599.RAOh-01iWApcoFZXVASC4YgMRRXIb4DOIKUyLyapw0b7s130_provenance.
- NP1599.RAOh-01iWApcoFZXVASC4YgMRRXIb4DOIKUyLyapw0b7s130_assertion SIO_000772 8168815 NP1599.RAOh-01iWApcoFZXVASC4YgMRRXIb4DOIKUyLyapw0b7s130_provenance.
- NP1599.RAOh-01iWApcoFZXVASC4YgMRRXIb4DOIKUyLyapw0b7s130_assertion wasDerivedFrom uniprot-20150221 NP1599.RAOh-01iWApcoFZXVASC4YgMRRXIb4DOIKUyLyapw0b7s130_provenance.
- NP1599.RAOh-01iWApcoFZXVASC4YgMRRXIb4DOIKUyLyapw0b7s130_assertion wasGeneratedBy ECO_0000218 NP1599.RAOh-01iWApcoFZXVASC4YgMRRXIb4DOIKUyLyapw0b7s130_provenance.
- uniprot-20150221 importedOn "2015-02-21" NP1599.RAOh-01iWApcoFZXVASC4YgMRRXIb4DOIKUyLyapw0b7s130_provenance.