Matches in Nanopublications for { <http://rdf.disgenet.org/nanopublications.trig#NP1638.RAd3xlzRonA9GUm6MziPMjlQ7rfmUbGZ3Qy1IZbCzUgus130_assertion> ?p ?o ?g. }
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- NP1638.RAd3xlzRonA9GUm6MziPMjlQ7rfmUbGZ3Qy1IZbCzUgus130_assertion type Assertion NP1638.RAd3xlzRonA9GUm6MziPMjlQ7rfmUbGZ3Qy1IZbCzUgus130_head.
- NP1638.RAd3xlzRonA9GUm6MziPMjlQ7rfmUbGZ3Qy1IZbCzUgus130_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." NP1638.RAd3xlzRonA9GUm6MziPMjlQ7rfmUbGZ3Qy1IZbCzUgus130_provenance.
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- NP1638.RAd3xlzRonA9GUm6MziPMjlQ7rfmUbGZ3Qy1IZbCzUgus130_assertion SIO_000772 8168815 NP1638.RAd3xlzRonA9GUm6MziPMjlQ7rfmUbGZ3Qy1IZbCzUgus130_provenance.
- NP1638.RAd3xlzRonA9GUm6MziPMjlQ7rfmUbGZ3Qy1IZbCzUgus130_assertion wasDerivedFrom uniprot-20130724 NP1638.RAd3xlzRonA9GUm6MziPMjlQ7rfmUbGZ3Qy1IZbCzUgus130_provenance.
- NP1638.RAd3xlzRonA9GUm6MziPMjlQ7rfmUbGZ3Qy1IZbCzUgus130_assertion wasGeneratedBy ECO_0000218 NP1638.RAd3xlzRonA9GUm6MziPMjlQ7rfmUbGZ3Qy1IZbCzUgus130_provenance.