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- source_evidence_literature type ECO_0000212 NP609383.RA_V2v547n1P17qpOlUXl19tw7LYdWIlBbSeP_dSTQB9M130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP609383.RA_V2v547n1P17qpOlUXl19tw7LYdWIlBbSeP_dSTQB9M130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP609383.RA_V2v547n1P17qpOlUXl19tw7LYdWIlBbSeP_dSTQB9M130_provenance.
- 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.
- befree-2016 importedOn "2016-02-19" NP609383.RA_V2v547n1P17qpOlUXl19tw7LYdWIlBbSeP_dSTQB9M130_provenance.