Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP4395.RASTC9NqaGpNzIILqEjT6xqp3PPMNJUEBkq3NT8_PNo9o130_provenance>. }
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- source_evidence_curated type ECO_0000205 NP4395.RASTC9NqaGpNzIILqEjT6xqp3PPMNJUEBkq3NT8_PNo9o130_provenance.
- source_evidence_curated label "DisGeNET evidence - CURATED" NP4395.RASTC9NqaGpNzIILqEjT6xqp3PPMNJUEBkq3NT8_PNo9o130_provenance.
- source_evidence_curated comment "Gene-disease associations manually curated." NP4395.RASTC9NqaGpNzIILqEjT6xqp3PPMNJUEBkq3NT8_PNo9o130_provenance.
- NP4395.RASTC9NqaGpNzIILqEjT6xqp3PPMNJUEBkq3NT8_PNo9o130_assertion wasGeneratedBy ECO_0000218 NP4395.RASTC9NqaGpNzIILqEjT6xqp3PPMNJUEBkq3NT8_PNo9o130_provenance.
- NP4395.RASTC9NqaGpNzIILqEjT6xqp3PPMNJUEBkq3NT8_PNo9o130_assertion wasDerivedFrom uniprot-20130724 NP4395.RASTC9NqaGpNzIILqEjT6xqp3PPMNJUEBkq3NT8_PNo9o130_provenance.
- NP4395.RASTC9NqaGpNzIILqEjT6xqp3PPMNJUEBkq3NT8_PNo9o130_assertion SIO_000772 8286749 NP4395.RASTC9NqaGpNzIILqEjT6xqp3PPMNJUEBkq3NT8_PNo9o130_provenance.
- NP4395.RASTC9NqaGpNzIILqEjT6xqp3PPMNJUEBkq3NT8_PNo9o130_assertion evidence source_evidence_curated NP4395.RASTC9NqaGpNzIILqEjT6xqp3PPMNJUEBkq3NT8_PNo9o130_provenance.
- NP4395.RASTC9NqaGpNzIILqEjT6xqp3PPMNJUEBkq3NT8_PNo9o130_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." NP4395.RASTC9NqaGpNzIILqEjT6xqp3PPMNJUEBkq3NT8_PNo9o130_provenance.
- uniprot-20130724 importedOn "2013-07-24" NP4395.RASTC9NqaGpNzIILqEjT6xqp3PPMNJUEBkq3NT8_PNo9o130_provenance.