Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP609383.RA_V2v547n1P17qpOlUXl19tw7LYdWIlBbSeP_dSTQB9M130_assertion> ?p ?o ?g. }
Showing items 1 to 6 of
6
with 100 items per page.
- NP609383.RA_V2v547n1P17qpOlUXl19tw7LYdWIlBbSeP_dSTQB9M130_assertion type Assertion NP609383.RA_V2v547n1P17qpOlUXl19tw7LYdWIlBbSeP_dSTQB9M130_head.
- NP609383.RA_V2v547n1P17qpOlUXl19tw7LYdWIlBbSeP_dSTQB9M130_assertion description "[Selected exonic sequencing of the AGXT gene provides a genetic diagnosis in 50% of patients with primary hyperoxaluria type 1.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP609383.RA_V2v547n1P17qpOlUXl19tw7LYdWIlBbSeP_dSTQB9M130_provenance.
- NP609383.RA_V2v547n1P17qpOlUXl19tw7LYdWIlBbSeP_dSTQB9M130_assertion evidence source_evidence_literature NP609383.RA_V2v547n1P17qpOlUXl19tw7LYdWIlBbSeP_dSTQB9M130_provenance.
- NP609383.RA_V2v547n1P17qpOlUXl19tw7LYdWIlBbSeP_dSTQB9M130_assertion SIO_000772 17495019 NP609383.RA_V2v547n1P17qpOlUXl19tw7LYdWIlBbSeP_dSTQB9M130_provenance.
- NP609383.RA_V2v547n1P17qpOlUXl19tw7LYdWIlBbSeP_dSTQB9M130_assertion wasDerivedFrom befree-2016 NP609383.RA_V2v547n1P17qpOlUXl19tw7LYdWIlBbSeP_dSTQB9M130_provenance.
- NP609383.RA_V2v547n1P17qpOlUXl19tw7LYdWIlBbSeP_dSTQB9M130_assertion wasGeneratedBy ECO_0000203 NP609383.RA_V2v547n1P17qpOlUXl19tw7LYdWIlBbSeP_dSTQB9M130_provenance.