Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP1334472.RA67DAsjoQOzZi7tB8YQwEQ5iSuXLyHQS_GswTYtXQ7-s130_assertion> ?p ?o ?g. }
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- NP1334472.RA67DAsjoQOzZi7tB8YQwEQ5iSuXLyHQS_GswTYtXQ7-s130_assertion type Assertion NP1334472.RA67DAsjoQOzZi7tB8YQwEQ5iSuXLyHQS_GswTYtXQ7-s130_head.
- NP1334472.RA67DAsjoQOzZi7tB8YQwEQ5iSuXLyHQS_GswTYtXQ7-s130_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." NP1334472.RA67DAsjoQOzZi7tB8YQwEQ5iSuXLyHQS_GswTYtXQ7-s130_provenance.
- NP1334472.RA67DAsjoQOzZi7tB8YQwEQ5iSuXLyHQS_GswTYtXQ7-s130_assertion evidence source_evidence_literature NP1334472.RA67DAsjoQOzZi7tB8YQwEQ5iSuXLyHQS_GswTYtXQ7-s130_provenance.
- NP1334472.RA67DAsjoQOzZi7tB8YQwEQ5iSuXLyHQS_GswTYtXQ7-s130_assertion SIO_000772 8168815 NP1334472.RA67DAsjoQOzZi7tB8YQwEQ5iSuXLyHQS_GswTYtXQ7-s130_provenance.
- NP1334472.RA67DAsjoQOzZi7tB8YQwEQ5iSuXLyHQS_GswTYtXQ7-s130_assertion wasDerivedFrom befree-2016 NP1334472.RA67DAsjoQOzZi7tB8YQwEQ5iSuXLyHQS_GswTYtXQ7-s130_provenance.
- NP1334472.RA67DAsjoQOzZi7tB8YQwEQ5iSuXLyHQS_GswTYtXQ7-s130_assertion wasGeneratedBy ECO_0000203 NP1334472.RA67DAsjoQOzZi7tB8YQwEQ5iSuXLyHQS_GswTYtXQ7-s130_provenance.